Next Article in Journal
Female Germ Cell Development, Functioning and Associated Adversities under Unfavorable Circumstances
Previous Article in Journal
Molecular Dissection of Escherichia coli CpdB: Roles of the N Domain in Catalysis and Phosphate Inhibition, and of the C Domain in Substrate Specificity and Adenosine Inhibition
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
IJMS
Volume 22
Issue 4
10.3390/ijms22041976
ijms-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

PrPC Aptamer Conjugated–Gold Nanoparticles for Targeted Delivery of Doxorubicin to Colorectal Cancer Cells

by
Gyeongyun Go
1,2,
Chang-Seuk Lee
3,
Yeo Min Yoon
4,
Ji Ho Lim
2,4,
Tae Hyun Kim
3,5,* and
Sang Hun Lee
1,2,4,*
1
Department of Biochemistry, Soonchunhyang University College of Medicine, Cheonan 31151, Korea
2
Department of Biochemistry, BK21FOUR Project2, College of Medicine, Soonchunhyang University, Cheonan 31151, Korea
3
Department of ICT Environmental Health System, Graduate School, Soonchunhyang University, Asan 31538, Korea
4
Medical Science Research Institute, Soonchunhyang University Seoul Hospital, Seoul 04401, Korea
5
Department of Chemistry, Soonchunhyang University, Asan 31538, Korea
*
Authors to whom correspondence should be addressed.
Int. J. Mol. Sci. 2021, 22(4), 1976; https://0-doi-org.brum.beds.ac.uk/10.3390/ijms22041976
Submission received: 2 January 2021 / Revised: 11 February 2021 / Accepted: 13 February 2021 / Published: 17 February 2021
(This article belongs to the Section Molecular Biology)
Browse Figures
Versions Notes

Abstract

:
Anticancer drugs, such as fluorouracil (5-FU), oxaliplatin, and doxorubicin (Dox) are commonly used to treat colorectal cancer (CRC); however, owing to their low response rate and adverse effects, the development of efficient drug delivery systems (DDSs) is required. The cellular prion protein PrPC, which is a cell surface glycoprotein, has been demonstrated to be overexpressed in CRC, however, there has been no research on the development of PrPC-targeting DDSs for targeted drug delivery to CRC. In this study, PrPC aptamer (Apt)-conjugated gold nanoparticles (AuNPs) were synthesized for targeted delivery of Dox to CRC. Thiol-terminated PrPC-Apt was conjugated to AuNPs, followed by hybridization of its complementary DNA for drug loading. Finally, Dox was loaded onto the AuNPs to synthesize PrPC-Apt-functionalized doxorubicin-oligomer-AuNPs (PrPC-Apt DOA). The PrPC-Apt DOA were spherical nanoparticles with an average diameter of 20 nm. Treatment of CRC cells with PrPC-Apt DOA induced reactive oxygen species generation by decreasing catalase and superoxide dismutase activities. In addition, treatment with PrPC-Apt DOA inhibited mitochondrial functions by decreasing the expression of peroxisome proliferator-activated receptor gamma coactivator 1-alpha, complex 4 activity, and oxygen consumption rates. Compared to free Dox, PrPC-Apt DOA decreased proliferation and increased apoptosis of CRC cells to a greater degree. In this study, we demonstrated that PrPC-Apt DOA targeting could effectively deliver Dox to CRC cells. PrPC-Apt DOA can be used as a treatment for CRC, and have the potential to replace existing anticancer drugs, such as 5-FU, oxaliplatin, and Dox.

1. Introduction

Colorectal cancer (CRC) is classified as one of the four major cancers, along with lung, breast, and prostate cancers [1]. In 2020, the total number of people diagnosed with CRC was estimated to be 147,950, which accounts for 8.2% of all cancers in the United States [1]. Chemotherapy is primarily used to kill the CRC cells remaining after surgery or for symptom relief in the later stages of cancer. Fluorouracil (5-FU) is mainly used as an anticancer agent for CRC, but it shows a low response rate of approximately 20% [2]. Oxaliplatin is also used for CRC treatment. Oxaliplatin is known to be effective in colorectal cancer cells which are resistant to other platinum-based anticancer drugs. In particular, oxaliplatin shows synergistic effects through combination treatment with 5-FU [3], but the response rate for each patient varies, from 20 to 50% [4,5,6]. Doxorubicin (Dox) is an anticancer agent that is most commonly used in chemotherapy, and known to bind to deoxyribonucleic acid (DNA), to inhibit DNA synthesis and induce apoptosis. Compared to other anticancer drugs, Dox has the advantage of being relatively cheap; however, CRC patients display resistance to it, Dox induces adverse effects including vomiting, hair loss, and cardiotoxicity [7]. To overcome these challenges, there is a need for safe and efficient drug delivery systems (DDSs) for Dox.
Various DDSs, such as micelles [8,9], superparamagnetic iron oxide nanoparticles [10,11], quantum dots [12,13], dendrimers [14], exosome mimetics [15,16], viral nanoparticles [17], and gold nanoparticles (AuNPs) [18,19] are being actively developed. Among these, AuNPs have several advantages as anticancer DDSs. First, AuNPs can be synthesized in various sizes and shapes. In addition, AuNPs can easily be modified through surface chemistry to display various types of molecules on the surface, which results in the functionalization of the AuNPs. As AuNPs are known to be potentially toxic, several studies have been conducted to overcome this issue through surface modification. Various biological materials, including DNA [20], polyethylene glycol (PEG) [21,22], polyamidoamine [23], cell-penetrating peptides, and chitosan [24,25] have been used to enhance the biocompatibility of AuNPs. Furthermore, nucleic acid components can also be used to enhance drug loading. For example, oligonucleotide-coated AuNPs can be loaded with the DNA-intercalating drug Dox with high efficiency [18,19].
The cellular prion protein (PrPC) is a glycophosphatidylinositol-anchored cell surface protein that is associated with diverse cellular functions, including stress protection and cellular differentiation [26]. Recently, several studies have shown that PrPC is highly expressed in various types of cancers, including gastric [27], pancreatic [28], breast cancers, and CRC [29,30]. Furthermore, it has been reported that PrPC promotes cancer progression by enhancing cancer cell proliferation, metastasis, and drug resistance. These results suggest that PrPC is a promising therapeutic target for cancer [29,30]. In this study, we hypothesized that an efficient targeted DDS could be developed for CRC treatment by targeting PrPC. In a previous study, we developed AuNPs coated with Dox-loaded oligonucleotides (Dox-oligomer-AuNP, DOA). In this study, we synthesized an oligonucleotide with an aptamer (Apt) sequence to target PrPC, which was then used to fabricate the PrPC-targeted Dox DDS (PrPC-Apt-functionalized doxorubicin-oligomer-AuNPs (PrPC-Apt DOA)) for CRC treatment. We evaluated the efficacy of PrPC-Apt DOA by determining the effect of PrPC-Apt DOA on the mitochondrial functions, proliferation, and apoptosis of CRC cells. Compared to free Dox, PrPC-Apt DOA significantly inhibited the mitochondrial function of CRCs. PrPC-Apt DOA also markedly inhibited the proliferation of CRCs and induced apoptosis. In developing cancer targeted DDSs, selecting an appropriate cancer target is important [31]. Until now, EGFR, HER2, folate receptor, and transferrin receptor have been mainly used as cancer targets [31]. In this study, we demonstrated that an effective cancer-targeted DDSs can be developed by targeting PrPC.

2. Results

2.1. Characterization of PrPC-Apt DOA

The AuNPs were synthesized by the thermal reduction in AuCl4− using citrate. To functionalize the AuNPs for PrPC targeting, thiol-terminated PrPC-Apt was conjugated to the AuNPs. The complementary DNA was hybridized for Dox loading. Finally, Dox was loaded onto the AuNPs to generate PrPC-Apt DOA (Figure 1A). The size of AuNPs is one of the important parameters that affects drug loading, cellular uptake, and in vivo targeting [32,33]. Because AuNPs have intrinsic self-aggregation properties, they may gradually increase in size or become crystallized over time [34]. Therefore, it is important to characterize AuNPs during preparation. A transmission electron microscopy image of AuNPs revealed that the AuNPs have spherical shapes with 13 nm of diameter suggesting successful synthesis of AuNPs (Supplemental Figure S1). Ultraviolet-visible (UV-Vis) spectroscopy and dynamic light scattering (DLS) analyses were conducted to characterize the size of PrPC-Apt DOA in the present study. Figure 1B shows the absorption spectra of AuNPs at each preparation step of PrPC-Apt DOA. All absorption spectra of AuNPs showed a similar shape and λmax of 520 nm, which indicated that the AuNPs had a diameter of 13 nm without aggregation, owing to electrostatic repulsive forces [35,36]. DLS analysis was conducted to measure the size distribution of PrPC-Apt DOA. As shown in Figure 1C, the average diameter of bare AuNPs was 13 nm and that of PrPC-Apt-conjugated AuNPs increased to 20 nm after the incubation of the bare AuNPs with the aptamers, suggesting successful immobilization of PrPC-Apt onto the AuNPs (Figure 1C). As Dox has an intrinsic fluorescence and quenching effect by photoelectron transfer (PET) from the π-electrons of intercalated DNA, the Dox loading amount of Apt-DOA was determined using fluorescence spectroscopy. The amount of Dox loaded onto complementary drug loading DNA (cDL-DNA), cDL-DNA/PrPC Apt, and cDL-DNA/PrPC Apt-AuNPs were determined to be 5.27, 7.97, and 798.25 molar equivalents (Dox/cDL-DNA, Dox/cDL-DNA/PrPC Apt, Dox/cDL-DNA/PrPC Apt-AuNPs), respectively (Figure 1D). Furthermore, we determined the fluorescence intensity of Dox which released from PrPC-Apt DOA in different conditions of pH and temperature. The initial-burst release was observed within 2 h in all the conditions, though the amount of Dox in pH 5.4 released was higher than pH 7.4. The fluorescence intensity of Dox showed negligible changes in different temperature condition of 25 °C and 36.5 °C (Supplemental Figure S2). These results indicate the possibility of a pH-triggered drug release of the PrPC-Apt DOA due to the acidic pH condition of the cancer microenvironment. Taken together, these results suggest that PrPC-Apt DOA are stable spherical nanoparticles, without aggregation or degradation. In addition, PrPC-Apt DOA serve as a promising DDS with a high drug-loading capacity, which is capable of loading a large amount of Dox.

2.2. PrPC-Apt DOA Show Active Targeting to PrPC-Positive CRC Cells

Next, we checked the active targeting of PrPC-Apt DOA to PrPC-positive CRC cells. First, we separated the PrPC-negative cells and PrPC-positive cells from SNU-C5 CRC cells using magnetic activated cell sorting. We determined the expression of PrPC in PrPC-negative and PrPC-positive cells and confirmed that PrPC expression is higher in the PrPC-positive cells (Figure 2A). Then, we evaluated PrPC targeting of PrPC-Apt DOA after the treatment of PrPC-Apt DOA to PrPC-negative and PrPC-positive cells. The flow cytometry results revealed that the uptake of PrPC-Apt DOA was significantly increased in PrPC-positive cells compared to PrPC-negative cells, suggesting the interaction of PrPC Apt and PrPC facilitates uptake of PrPC-Apt DOA (Figure 2B). We further confirmed the PrPC targeting of PrPC-Apt DOA using fluorescence microscopy. The results showed that the fluorescence intensity of Dox was greatly increased in PrPC-positive CRC cells. These results indicate that PrPC-Apt DOA can efficiently deliver Dox by targeting PrPC.

2.3. PrPC-Apt DOA Increase Reactive Oxygen Species (ROS) Formation by Decreasing Catalase and Superoxide Dismutase (SOD) Activities

As Dox treatment is known to induce ROS formation, we first determined the effect of PrPC-Apt DOA on ROS formation. To determine whether PrPC-Apt DOA inhibit the catalase activity of CRC cells, SNU-C5 cells were treated with PrPC-Apt DOA, followed by measurement of the catalase activity. As shown in Figure 3A, treatment of SNU-C5 cells with PrPC-Apt DOA (2.5 nM of PrPC-Apt DOA containing 2 μM of Dox, 48 h) caused a greater decrease in the catalase activity, as compared to treatment with an equivalent concentration of free Dox (2 μM, 48 h). To further determine the effect of PrPC-Apt DOA on SOD activity, SNU-C5 cells were treated with PrPC-Apt DOA or free Dox, and the SOD activity was measured. As expected, treatment with PrPC-Apt DOA caused a greater decrease in the SOD activity of SNU-C5 cells, as compared to an equivalent concentration of free Dox (Figure 3B). Finally, we performed flow cytometry analysis of PrPC-Apt DOA or free Dox-treated SNU-C5 cells post dihydroethidium (DHE) staining. Since DHE is oxidized by ROS and become fluorescent, the ROS generation in live cells can be represented as total DHE fluorescence. DHE staining results showed that PrPC-Apt DOA significantly increased ROS formation in SNU-C5 cells (Figure 3C). These results indicate that PrPC-Apt DOA efficiently increased ROS formation in CRC cells by decreasing catalase and SOD activities.

2.4. PrPC-Apt DOA Efficiently Inhibit the Mitochondrial Function of CRC Cells

To determine whether PrPC-Apt DOA affects the mitochondrial function of CRC cells, we performed western blot analysis of PrPC-Apt DOA-treated CRC cells for peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC-1α) expression. PGC-1α is a transcriptional coactivator that regulates cellular energy metabolism. PGC-1α enhances mitochondrial function and promotes mitochondrial biogenesis [37]. Compared to treatment with free Dox, treatment with PrPC-Apt DOA further decreased the expression of PGC-1α in CRC cells (Figure 4A). Next, we determined the effect of PrPC-Apt DOA on the activity of mitochondrial complex IV and the mitochondrial membrane potential. As expected, treatment with PrPC-Apt DOA significantly decreased the complex IV activity and tetramethylrhodamine ethyl ester (TMRE)-positive population in CRC cells (Figure 4B,C). Next, we further confirmed the effect of PrPC-Apt DOA on mitochondrial function by measuring the oxygen consumption rate (OCR) of the CRC cells. Treatment with PrPC-Apt DOA significantly decreased basal respiration and proton leak in the mitochondria of CRC cells, with no effect on maximal respiration and ATP production (Figure 5A–E). These results suggest that PrPC-Apt DOA efficiently delivered Dox into the CRC cells, decreased PGC-1α expression, and inhibited the mitochondrial function of CRC cells.

2.5. PrPC-Apt DOA Efficiently Inhibit Proliferation of CRC Cells in Addition to Promoting Apoptosis

To determine the effect of PrPC-Apt DOA on the proliferation of CRC cells, we performed cell cycle analysis using flow cytometry. The results revealed that PrPC-Apt DOA significantly decreased the percentage of cells in S-phase from 21.6% to 6.3%, while free Dox caused only a slight decrease in the same (from 21.6% to 16.6%) (Figure 6A). To further determine whether PrPC-Apt DOA inhibit the proliferation of CRC cells, western blot analysis was performed for cell cycle-associated proteins, such as cyclin-dependent kinase (CDK) 2, cyclin E, CDK4, and cyclin D1. Treatment with PrPC-Apt DOA resulted in a greater decrease in the expression of cell cycle-related proteins, as compared to treatment with free Dox (Figure 6B). To determine whether treatment with PrPC-Apt DOA increased the number of dead cells in CRC cells, live and dead cells were quantified in free Dox- or PrPC-Apt DOA-treated SNU-C5 cells. As shown in Figure 7A, treatment with PrPC-Apt DOA significantly increased the percentage of dead cells, compared to treatment with free Dox (Figure 7A). Next, Annexin V/propidium iodide (PI) flow cytometry analysis was performed to investigate whether PrPC-Apt DOA increase apoptosis in CRC cells. Treatment with PrPC-Apt DOA further increased the percentage of early and late apoptosis to 67%, compared to that in the free Dox-treated group (27%) (Figure 7B). Consistent with these results, western blot analysis demonstrated that treatment with PrPC-Apt DOA further decreased the expression of B-cell lymphoma 2 (BCL2) and increased that of Bcl-2-associated X protein (BAX) and cleaved caspase-3, as compared to that with free Dox treatment (Figure 7C). Taken together, these results suggest that PrPC-Apt DOA effectively inhibited proliferation and increased apoptosis by efficiently delivering Dox to CRC cells by targeting PrPC.

2.6. PrPC-Apt DOA Efficiently Inhibit the Sphere Formation Capacity of CRC Cells

The sphere formation assay is often used to assess the stem cell properties of cancer cells. We determined whether PrPC-Apt DOA inhibit the sphere formation capacity of CRC cells. SNU-C5 cells were cultured in ultra-low attachment six-well plates for 14 d in the presence of free Dox or PrPC-Apt DOA. As shown in Figure 8A, while free Dox also inhibited sphere formation of CRC cells, PrPC-Apt DOA efficiently inhibited sphere formation in SNU-C5 cells, as compared to free DOX. The diameters of the spheres were significantly reduced in PrPC-Apt-DOA-treated SNU-C5 cells (Figure 8B). These results suggest that PrPC-Apt DOA not only increased the apoptosis of CRC cells, but also inhibited the cancer stem cell properties of CRC cells.

3. Discussion

In this study, we developed PrPC-targeting AuNPs as an anti-cancer DDS. PrPC-Apt-conjugated AuNPs synthesized in this study were spherical nanoparticles with an average diameter of 20 nm. PrPC-Apt AuNPs displayed efficient loading of Dox and PrPC-targeted delivery of Dox to CRC cells. PrPC-Apt DOA efficiently inhibited the function of mitochondria, cell proliferation, and induced apoptosis of CRC cells, as compared to free Dox. In addition, PrPC-Apt DOA efficiently decreased the sphere formation capacity of CRC cells. These results suggest that active targeted drug delivery to CRC can be achieved by targeting PrPC. Thus, PrPC-Apt DOA may replace oxaliplatin and 5-FU as effective therapeutic agents that can be used in CRC treatment.
Compared to other nano-based DDSs, such as liposomes, iron oxide nanoparticles, and quantum dots, AuNPs have several advantages as DDSs; specifically, AuNPs are capable of being synthesized in different sizes and shapes, and allow for ease of surface modification. In addition, AuNPs can be loaded with various types of drugs, including chemical drugs [38,39,40], oligonucleotides [41], proteins [42], and vaccines [43]. Furthermore, DNA-conjugated AuNPs can be used as pH-dependent targeted DDSs, as the G and C bases are depurinated under acidic conditions, leading to the structural transformation of double-stranded DNA and Dox. The surface of AuNPs can be modified with various molecules, such as PEG [44], peptides [45], antibodies [46], or aptamers [47,48] to enhance their stability or to functionalize the NPs for targeted delivery systems. The prostate-specific membrane antigen (PSMA)-targeting aptamer, A10, was conjugated to the surface of AuNPs, and these A10-conjugated AuNPs display high sensitivity and specificity towards PSMA-expressing prostate cancer cells [49]. In addition, Ramos cell aptamer-conjugated AuNPs display specific recognition of tumor sites [50]. In this study, we conjugated PrPC aptamers to AuNPs for Dox delivery to CRC. The AuNPs efficiently delivered Dox to PrPC-positive CRC cells and induced ROS generation, mitochondrial damage, and apoptosis.
We developed Dox DDSs using PrPC aptamer-functionalized AuNPs. Many similar studies on the development of AuNP-based Dox DDSs have been reported [51]. Ramalingam et al. developed Dox DDSs by loading Dox into polyvinylpyrrolidone (PVP)-stabilized AuNPs [52]. The Dox-loaded PVP-AuNPs induced increased ROS generation and apoptosis in lung cancer compared to free Dox and PVP-AuNPs without Dox. Similarly, Du et al. also developed AuNP-based Dox DDSs by directly conjugating thoiolated doxorubicin analogs to PEG-modified AuNPs [39]. The doxorubicin analogs contain glutathione-reactive moiety, which facilitates Dox release under a reducing tumor environment. Although these Dox DDSs showed efficient Dox loading and anticancer efficacy, they lack cancer targeting ligands, which may reduce cancer-specific delivery. Many studies on active targeting of drug-loaded AuNPs using cancer targeting ligands such as antibodies, peptides, and small molecules also have been reported [53]. Zhang et al. developed 5-fluorodeoxyuridine (FUdR) and Dox co-delivery systems using HER2-specific affibody-functionalized AuNPs [54]. They conjugated FUdR containing DNA to HER2-specifc affibody and attached the affibody-DNA hybrid to AuNPs. However, displaying antibodies or small molecules on the surface of AuNPs requires additional synthetic reactions, which may complicate the development process and increase batch-to-batch variation and difficulty in mass production.
Aptamers have several advantages as cancer targeting ligands since they are easy to synthesize, stable, non-immunogenic, and low-cost. A recent review found that EpCAM and Mucin-1 have been the most popular aptamer targets for CRC [55]. Mashreghi et al. developed CRC-targeted Dox DDSs using an SYL3C aptamer (which targets EpCAM)-functionalized liposomes [56]. Moosavian et al. utilized the 5TR1-aptamer, which targets Mucin1, for the development of PEGylated liposomal Dox DDSs [57]. However, the Kd value of SYL3C aptamer and 5TR1 aptamer are known as 38 nM [58] and 21 nM [59], respectively, which is higher than that of PrPC aptamer of 16 nM [60]. Although PrPC is overexpressed in CRC, and PrPC aptamer is promising for CRC targeting, the development of CRC-targeted DDSs using PrPC aptamer has been lacking. Du et al. developed the AuNPs-DNA (Dox) which is a Dox delivery system using PrPC aptamer-functionalized AuNPs [61]. The AuNPs-DNA (Dox) looks similar to our PrPC-Apt DOA in that it is composed of AuNPs, PrPC aptamer, and Dox. However, AuNPs-DNA (Dox) and PrPC-Apt DOA show differences in terms of DNA structure. In AuNPs-DNA (Dox), Dox is loaded at double-strand CG sequences in the stem region and the PrPC aptamer is located at the loop region. Upon binding of PrPC aptamer to PrPC, double-strand DNA structure is destroyed and Dox are released from DNA, which may reduce drug delivery efficiency. However, in PrPC-Apt DOA, even if the PrPC aptamer binds to PrPC, it does not affect the structure of double-strand DNA and the Dox release. In addition, AuNPs-DNA (Dox) is used for human bone marrow neuroblastoma, whereas PrPC-Apt DOA is used for CRC cells.
Although PrPC-Apt DOA is an excellent DDS for CRC, it is necessary to improve PrPC-Apt DOA compared to other DDSs. PrPC-Apt DOA can be loaded with other drugs such as photosensitizers [62] and therapeutic nucleic acids [63] to develop co-delivery systems, which would show better therapeutic effects for Dox-resistant CRC. In addition, by changing the shapes, sizes and organizations of PrPC-Apt DOA, we may improve plasmonic photothermal properties and use them as phototheramal agents [64].
AuNPs are in the spotlight as promising DDSs since they are easy to synthesize, have excellent stability, and have the potentials to be used in various biomedical applications [65]. However, at the same time, the toxicity of AuNPs is being raised as an important issue [66]. Factors involved in the toxicity of AuNPs include size and shape, and surface chemistry of AuNPs [66,67]. In particular, it is known that the toxicity of AuNP can be significantly reduced through surface modification. In general, PEG is widely used to reduce the toxicity of AuNPs [22,68]. Patlolla et al. showed that the PEG coating of AuNPs reduced the ROS generation and hepatotoxicity compared to uncoated AuNPs [69]. In our previous study, DNA-conjugated AuNPs did not show toxicity in three human ovarian cancer cell lines, SK-OV-3, HEY A8, and A2780 [19]. However, further studies are needed to minimize the toxicity of AuNP by modifying the size, shape, and surface chemistry to promote applications of AuNPs in biomedicine.
In conclusion, we developed a PrPC-targeted Dox DDS. We demonstrated that PrPC-Apt DOA efficiently delivered Dox to CRC cells and induced ROS generation, mitochondrial damage, and apoptosis, as compared to free Dox. These results suggest that PrPC-APT DOA can serve as an effective therapeutic agent for CRC treatment. Future studies need to evaluate the in vivo safety, targeting, and anti-tumor effects of Prion Apt-DOA in CRC xenograft models, to assess the potential of this DDS.

4. Materials and Methods

4.1. Materials

Gold(III) chloride trihydrate, Dox hydrochloride, sodium citrate tribasic dihydrate, DHE, and phosphate-buffered saline (PBS) were purchased from Sigma-Aldrich. Thiol-terminated PrPC aptamer DNA (5′-HS-C6-AAAAAAAAAA-TCG-TCG-TCG-TCG-TCG-TCG-TCG-CGGTGGGGCAATTTCTCCTACTGT-3′, underlined sequence is for the PrPC aptamer) and cDL-DNA (5′-CGA-CGA-CGA-CGA-CGA-CGA-CGA-3′) were obtained from GenoTech (Daejeon, Republic of Korea).

4.2. Synthesis of PrPC-Apt DOA

PrPC-Apt DOA were synthesized according to a previously reported protocol [18]. AuNPs were synthesized in a single phase using a thermal reduction method with a trisodium citrate dihydrate reduction agent. First, 1 mL of 38.8 mM sodium citrate dihydrate solution was added rapidly to 10 mL of 1 mM HAuCl4 boiling solution. The reaction was stopped when the color of the solution changed from yellow to deep red. It is known that the color of the reaction mixture changes from yellow to deep red during the synthesis. Gold nanoparticles larger than 2 nm in diameter exhibit the characteristic surface plasmon band and such particles appear deep red [70]. The AuNP solution was then cooled to room temperature with stirring. To modify the AuNPs with PrPC-Apt, 100 μL of 10 μM PrPC-Apt was added to 1 mL of 10 nM AuNPs. The mixed solution was then incubated in a shaking incubator at 350 rpm and 25 °C for 16 h. Before further incubation, 100 μL of 1 M sodium chloride and 100 μL of 0.1 M phosphate buffer were added to the mixed solution. After incubation, the mixed solution was purified by centrifuging the PrPC-Apt and AuNPs mixed solution at 13,500 rpm for 20 min. To hybridize PrPC-Apt and cDL-DNA, 100 μL of 10 μM cDL-DNA was added to the PrPC-Apt/AuNPs solution at 350 rpm, 95 °C for 5 min. The mixed solution was then incubated in a shaking incubator at 350 rpm and 25 °C for 1 h. The PrPC-Apt/cDL-DNA/AuNPs solution was then purified by centrifuging twice at 13,500 rpm for 20 min. Finally, for loading of PrPC-Apt/AuNPs with Dox, 100 μL of 100 μM Dox was added to 1 mL of PrPC-Apt/AuNPs and incubated in a shaking incubator at 350 rpm, 25 °C for 1 h. The mixed solution was then purified by centrifuging twice at 13,500 rpm for 20 min.

4.3. Characterization of PrPC-Apt DOA

The particle size of AuNPs at each experimental step was confirmed using a S-3100 UV-Vis spectrophotometer (Scinco Co. Ltd., Seoul, Korea) and a Zetasizer Nano ZS-90 DLS instrument (Malvern Panalytical, UK). The binding ratios of Dox to cDL-DNA, cDL-DNA/PrPC-Apt, and cDL-DNA/PrPC-Apt/AuNPs were measured using fluorescence spectroscopy with an FS-2 instrument (Scinco Co. Ltd.), at excitation and emission wavelengths of 480 and 592 nm, respectively. The loading capacity was calculated by methods used in our previous study [18]. For the drug loading capacity of PrPC-Apt DOA, the fluorescence of Dox was measured by fluorescence spectroscopy. Firstly, Dox was added into the 0.1 μM of cDL-DNA, cDL-DNA/PrPC-Apt, and cDL-DNA/PrPC-Apt+AuNP with 1 h of binding time. Then, the samples were purified by centrifugation at 13,500 rpm for 20 min twice.

4.4. Culture of Human CRC Cell Line

The human CRC SNU-C5 cells (available from Korea Cell Line Bank, 0000C5) were obtained from the Chosun University Research Center for Resistant Cells (Gwangju, Republic of Korea). The cells were grown in RPMI 1640 medium (Thermo Fisher Scientific, Waltham, MA, USA) containing 10% fetal bovine serum, L-glutamine, and antibiotics (Thermo Fisher Scientific) at 37 °C in a 5% CO2-humidified incubator.

4.5. DHE Staining

DHE was used to measure superoxide anion levels in PrPC-Apt DOA-treated SNU-C5 cells. The PrPC-Apt DOA-treated SNU-C5 cells were treated with 10 mM DHE for 30 min at 37 °C. DHE-positive cells were detected using a CyFlow® Cube 8 instrument (Partec, Munster, Germany), after washing with PBS. FSC Express 5 software (De Novo Software, Los Angeles, CA, USA) was used for data analysis.

4.6. Measurement of Mitochondrial Membrane Potential

To measure the mitochondrial membrane potential of PrPC-Apt DOA or free Dox-treated (2 μM, 48 h) SNU-C5 cells, TMRE (Abcam, Cambridge, UK) was used to stain the cells. The PrPC-Apt DOA-treated or free Dox-treated SNU-C5 cells were trypsinized and then centrifuged. After washing with PBS, the cells were stained with 200 nM TMRE solution in PBS at 37 °C for 15 min. TMRE-positive cells were detected using flow cytometry (Sysmex, Kobe, Japan).

4.7. Cell Cycle Analysis

SNU-C5 cells treated with free Dox or PrPC-Apt DOA (2 μM, 48 h) were collected and fixed with 70% ethanol at −20 °C for 2 h. After washing with cold PBS, the cells were treated with FxCycle™ PI/RNase staining solution (Thermo Fisher Scientific) at 4 °C for 1 h. Cell cycle analysis was carried out using flow cytometry (Sysmex). Events were recorded for at least 104 cells per sample. The sample data were analyzed using FCS Express 5 software (DeNovo Software).

4.8. Catalase Activity Assay

For the measurement of catalase activity, 40 μg of whole cell lysates were treated with 20 mM H2O2 in 0.1 M Tris-HCl for 30 min. The sample was further treated with 50 mM Amplex Red reagent (Thermo Fisher Scientific) and 0.2 U/mL horseradish peroxidase (HRP) and incubated for 30 min at 37 °C. The decomposition of the substrate was measured using a microplate reader (Varioskan™ LUX, Thermo Fisher Scientific) at the wavelength of 563 nm with measurement time of 100 ms at 20 °C.

4.9. SOD Activity Assay

SNU-C5 cells were collected and lysed with RIPA buffer (Thermo Fisher Scientific). Whole cell lysates (total 50 μg of protein) were treated with SOD, an enzyme that catalyzes potentially harmful ROS in cells, and the signal was immediately measured, every minute for 15 min, at the wavelength of 450 nm using a microplate reader (Varioskan™ LUX). The measurement time was set at 100 ms and the measurement temperature was 20 °C.

4.10. Western Blotting

Whole cell lysates of free Dox- or PrPC-Apt DOA-treated SNU-C5 cells were separated using 8–12% SDS-PAGE and then transferred to PVDF membranes. Membranes were blocked using 3% skimmed milk for 1 h, followed by overnight incubation at 4 °C with primary antibodies against PGC-1α, CDK2, cyclin E, CDK4, cyclin D1, BCL2, BAX, cleaved caspase-3, and β-actin. After washing with TBST (with 0.05% Tween-20), the membranes were incubated with goat anti-rabbit IgG or goat anti-mouse IgG conjugated to HRP (Santa Cruz Biotechnology, Santa Cruz, CA, USA). The bands were detected using enhanced chemiluminescence (Amersham Pharmacia Biotech, England, UK). Mouse anti-PGC-1α antibody (NBP1-04676) was obtained from Novus Biologicals (Littleton, CO, USA). The mouse anti-CDK2 (SC-6248), mouse anti-cyclin E (SC-377100), mouse anti-CDK4 (SC-56277), mouse anti-cyclin D1 (SC-20044), mouse anti-BCL2 (SC-7382), rabbit anti-Bax (SC-6236), rabbit anti-cleaved caspase-3 (SC-7148), and mouse anti-β-actin (SC-47778) antibodies were purchased from Santa Cruz Biotechnology.

4.11. Mitochondrial Complex IV Activity Assays

Mitochondrial fractions isolated from free Dox- or PrPC-Apt DOA-treated SNU-C5 cells were incubated in the assay medium for 3 min. Complex IV activity was analyzed by adding 75 mL of cytochrome c previously reduced with sodium borohydride and measuring the absorbance at the wavelength of 550 nm. The assay medium was composed of 0.8 μmol/L antimycin, 50 μmol/L decylubiquinone, 1 mmol/L potassium cyanide, 50 mmol/L potassium phosphate, and 250 mmol/L sucrose, pH 7.4.

4.12. OCR Measurement

OCR was measured in SNU-C5 CRC cells using the XF96 Extracellular Flux Analyzer (Seahorse Bioscience, MA, USA). Briefly, SNU-C5 CRC cells were added at a density of 5.0 × 104 cells/well into XF96 cell culture multi-well plates and incubated overnight at 37 °C in a 5% CO2-humidified incubator. XF calibrant was added to the XF96 cartridges, following which the cartridges were incubated overnight at 37 °C in a non-CO2 incubator. The cell growth medium was changed to XF medium and the cells were further incubated at 37 °C in a non-CO2 incubator for 1 h. Next, inhibitors, including oligomycin, FCCP, and antimycin A were diluted to the appropriate concentrations in XF medium and added into the corresponding microwells of the XF96 cartridge plates. Following equilibration of the sensor cartridges, the XF96 cell culture multi-well plates were loaded into the XF96 Extracellular Flux Analyzer for measurement of the OCR. OCR were measured every 7 min (after mixing for 3 min, waiting for 2 min, and measurement for 2 min), 3 times after injection of the respective compounds (1.5 μM oligomycin, 1 μM FCCP, and 0.5 μM Rotenone + Antimycin A). Seahorse Wave Desktop Software (Agilent Technologies, Santa Clara, CA, USA) was used for the analysis.

4.13. Spheroid Culture

SNU-C5 CRC cells treated with free Dox or PrPC-Apt DOA were cultured in ultra-low attachment six-well plates (Corning, Corning, NY, USA) for spheroid formation. The CRC cells were incubated in RPMI 1640 medium and grown at 37 °C in a 5% CO2-humidified atmosphere. Spheroids were grown for 14 d and observed using an optical inverted microscope (Olympus, Tokyo, Japan).

Supplementary Materials

The following are available online at https://0-www-mdpi-com.brum.beds.ac.uk/1422-0067/22/4/1976/s1.

Author Contributions

G.G.: data analysis and drafting of the manuscript; C.-S.L.: data collection and data analysis; Y.M.Y.: data collection and data analysis; J.H.L.: data collection and data analysis; T.H.K.: designing the study and drafting of the manuscript; S.H.L.: designing the study, drafting, and editing of the manuscript, and procurement of funding. All authors have read and agreed to the published version of the manuscript.

Funding

This research was supported by the National Research Foundation of Korea (NRF) grant funded by the Korea Government (MSIT) (2016R1D1A3B01007727, No. NRF2020R1A2C1014918).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest. The funders had no role in the study design, collection and analysis of data, decision to publish, or preparation of the manuscript.

References

  1. Siegel, R.L.; Miller, K.D.; Jemal, A. Cancer statistics, 2020. CA Cancer J. Clin. 2020, 70, 7–30. [Google Scholar] [CrossRef] [PubMed]
  2. Erlichman, C.; Fine, S.; Wong, A.; Elhakim, T. A randomized trial of fluorouracil and folinic acid in patients with metastatic colorectal carcinoma. J. Clin. Oncol. 1988, 6, 469–475. [Google Scholar] [CrossRef] [PubMed]
  3. Raymond, E.; Buquet-Fagot, C.; Djelloul, S.; Mester, J.; Cvitkovic, E.; Allain, P.; Louvet, C.; Gespach, C. Antitumor activity of oxaliplatin in combination with 5-fluorouracil and the thymidylate synthase inhibitor AG337 in human colon, breast and ovarian cancers. Anticancer Drugs 1997, 8, 876–885. [Google Scholar] [CrossRef] [PubMed]
  4. de Gramont, A.; Vignoud, J.; Tournigand, C.; Louvet, C.; Andre, T.; Varette, C.; Raymond, E.; Moreau, S.; Le Bail, N.; Krulik, M. Oxaliplatin with high-dose leucovorin and 5-fluorouracil 48-hour continuous infusion in pretreated metastatic colorectal cancer. Eur. J. Cancer 1997, 33, 214–219. [Google Scholar] [CrossRef]
  5. Levi, F.; Zidani, R.; Misset, J.L. Randomised multicentre trial of chronotherapy with oxaliplatin, fluorouracil, and folinic acid in metastatic colorectal cancer. International Organization for Cancer Chronotherapy. Lancet 1997, 350, 681–686. [Google Scholar] [CrossRef]
  6. Suh, S.H.; Kwon, H.C.; Jo, J.H.; Cho, Y.R.; Seo, B.G.; Lee, D.M.; Kim, S.H.; Kim, J.S.; Kim, H.J. Oxaliplatin with biweekly low dose leucovorin and bolus and continuous infusion of 5-fluorouracil (modified FOLFOX 4) as a salvage therapy for patients with advanced gastric cancer. Cancer Res. Treat. 2005, 37, 279–283. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  7. Sonowal, H.; Pal, P.B.; Wen, J.J.; Awasthi, S.; Ramana, K.V.; Srivastava, S.K. Aldose reductase inhibitor increases doxorubicin-sensitivity of colon cancer cells and decreases cardiotoxicity. Sci. Rep. 2017, 7, 3182. [Google Scholar] [CrossRef]
  8. Majumder, N.; Das, N.G.; Das, S.K. Polymeric micelles for anticancer drug delivery. 2020, 11, 613–635. [Google Scholar] [CrossRef] [PubMed]
  9. Lu, Y.; Yue, Z.; Xie, J.; Wang, W.; Zhu, H.; Zhang, E.; Cao, Z. Micelles with ultralow critical micelle concentration as carriers for drug delivery. Nat. Biomed. Eng. 2018, 2, 318–325. [Google Scholar] [CrossRef]
  10. Zhi, D.; Yang, T.; Yang, J.; Fu, S.; Zhang, S. Targeting strategies for superparamagnetic iron oxide nanoparticles in cancer therapy. Acta Biomater 2020, 102, 13–34. [Google Scholar] [CrossRef]
  11. Xie, L.; Jin, W.; Chen, H.; Zhang, Q. Superparamagnetic Iron Oxide Nanoparticles for Cancer Diagnosis and Therapy. J. Biomed. Nanotechnol. 2019, 15, 215–416. [Google Scholar] [CrossRef]
  12. Su, W.; Guo, R.; Yuan, F.; Li, Y.; Li, X.; Zhang, Y.; Zhou, S.; Fan, L. Red-Emissive Carbon Quantum Dots for Nuclear Drug Delivery in Cancer Stem Cells. J. Phys. Chem. Lett. 2020, 11, 1357–1363. [Google Scholar] [CrossRef] [PubMed]
  13. Iannazzo, D.; Pistone, A.; Celesti, C.; Triolo, C.; Patane, S.; Giofre, S.V.; Romeo, R.; Ziccarelli, I.; Mancuso, R.; Gabriele, B.; et al. A Smart Nanovector for Cancer Targeted Drug Delivery Based on Graphene Quantum Dots. Nanomaterials 2019, 9, 282. [Google Scholar] [CrossRef] [Green Version]
  14. Li, J.; Liang, H.; Liu, J.; Wang, Z. Poly (amidoamine) (PAMAM) dendrimer mediated delivery of drug and pDNA/siRNA for cancer therapy. Int J. Pharm 2018, 546, 215–225. [Google Scholar] [CrossRef] [PubMed]
  15. Jang, S.C.; Kim, O.Y.; Yoon, C.M.; Choi, D.S.; Roh, T.Y.; Park, J.; Nilsson, J.; Lotvall, J.; Kim, Y.K.; Gho, Y.S. Bioinspired exosome-mimetic nanovesicles for targeted delivery of chemotherapeutics to malignant tumors. Acs Nano 2013, 7, 7698–7710. [Google Scholar] [CrossRef] [PubMed]
  16. Go, G.; Lee, J.; Choi, D.S.; Kim, S.S.; Gho, Y.S. Extracellular Vesicle-Mimetic Ghost Nanovesicles for Delivering Anti-Inflammatory Drugs to Mitigate Gram-Negative Bacterial Outer Membrane Vesicle-Induced Systemic Inflammatory Response Syndrome. Adv. Healthc Mater. 2019, 8, e1801082. [Google Scholar] [CrossRef]
  17. Aljabali, A.A.; Shukla, S.; Lomonossoff, G.P.; Steinmetz, N.F.; Evans, D.J. CPMV-DOX delivers. Mol. Pharm. 2013, 10, 3–10. [Google Scholar] [CrossRef] [Green Version]
  18. Lee, C.S.; Kim, H.; Yu, J.; Yu, S.H.; Ban, S.; Oh, S.; Jeong, D.; Im, J.; Baek, M.J.; Kim, T.H. Doxorubicin-loaded oligonucleotide conjugated gold nanoparticles: A promising in vivo drug delivery system for colorectal cancer therapy. Eur. J. Med. Chem. 2017, 142, 416–423. [Google Scholar] [CrossRef]
  19. Lee, C.S.; Kim, T.W.; Oh, D.E.; Bae, S.O.; Ryu, J.; Kong, H.; Jeon, H.; Seo, H.K.; Jeon, S.; Kim, T.H. In Vivo and In Vitro Anticancer Activity of Doxorubicin-loaded DNA-AuNP Nanocarrier for the Ovarian Cancer Treatment. Cancers 2020, 12, 634. [Google Scholar] [CrossRef] [Green Version]
  20. Liu, B.; Liu, J. Interface-Driven Hybrid Materials Based on DNA-Functionalized Gold Nanoparticles. Matter 2019, 1, 825–847. [Google Scholar] [CrossRef] [Green Version]
  21. Spinelli, A.; Girelli, M.; Arosio, D.; Polito, L.; Podini, P.; Martino, G.; Seneci, P.; Muzio, L.; Menegon, A. Intracisternal delivery of PEG-coated gold nanoparticles results in high brain penetrance and long-lasting stability. J. Nanobiotechnology 2019, 17, 49. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  22. Chen, T.Y.; Chen, M.R.; Liu, S.W.; Lin, J.Y.; Yang, Y.T.; Huang, H.Y.; Chen, J.K.; Yang, C.S.; Lin, K.M. Assessment of Polyethylene Glycol-Coated Gold Nanoparticle Toxicity and Inflammation In Vivo Using NF-kappaB Reporter Mice. Int. J. Mol. Sci. 2020, 21, 8158. [Google Scholar] [CrossRef] [PubMed]
  23. Xu, Z.; Wang, Y.; Ma, Z.; Wang, Z.; Wei, Y.; Jia, X. A poly(amidoamine) dendrimer-based nanocarrier conjugated with Angiopep-2 for dual-targeting function in treating glioma cells. Polym. Chem. 2016, 7, 715–721. [Google Scholar] [CrossRef]
  24. Martinez-Torres, A.C.; Zarate-Trivino, D.G.; Lorenzo-Anota, H.Y.; Avila-Avila, A.; Rodriguez-Abrego, C.; Rodriguez-Padilla, C. Chitosan gold nanoparticles induce cell death in HeLa and MCF-7 cells through reactive oxygen species production. Int. J. Nanomed. 2018, 13, 3235–3250. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  25. Bhumkar, D.R.; Joshi, H.M.; Sastry, M.; Pokharkar, V.B. Chitosan reduced gold nanoparticles as novel carriers for transmucosal delivery of insulin. Pharm. Res. 2007, 24, 1415–1426. [Google Scholar] [CrossRef] [Green Version]
  26. Castle, A.R.; Gill, A.C. Physiological Functions of the Cellular Prion Protein. Front. Mol. Biosci. 2017, 4, 19. [Google Scholar] [CrossRef] [Green Version]
  27. Liang, J.; Luo, G.; Ning, X.; Shi, Y.; Zhai, H.; Sun, S.; Jin, H.; Liu, Z.; Zhang, F.; Lu, Y.; et al. Differential expression of calcium-related genes in gastric cancer cells transfected with cellular prion protein. Biochem. Cell Biol. 2007, 85, 375–383. [Google Scholar] [CrossRef]
  28. Li, Q.Q.; Cao, X.X.; Xu, J.D.; Chen, Q.; Wang, W.J.; Tang, F.; Chen, Z.Q.; Liu, X.P.; Xu, Z.D. The role of P-glycoprotein/cellular prion protein interaction in multidrug-resistant breast cancer cells treated with paclitaxel. Cell Mol. Life Sci. 2009, 66, 504–515. [Google Scholar] [CrossRef]
  29. Go, G.; Lee, S.H. The Cellular Prion Protein: A Promising Therapeutic Target for Cancer. Int. J. Mol. Sci. 2020, 21, 9208. [Google Scholar] [CrossRef]
  30. Go, G.; Yun, C.W.; Yoon, Y.M.; Lim, J.H.; Lee, J.H.; Lee, S.H. Role of PrP(C) in Cancer Stem Cell Characteristics and Drug Resistance in Colon Cancer Cells. Anticancer Res. 2020, 40, 5611–5620. [Google Scholar] [CrossRef] [PubMed]
  31. Kutova, O.M.; Guryev, E.L.; Sokolova, E.A.; Alzeibak, R.; Balalaeva, I.V. Targeted Delivery to Tumors: Multidirectional Strategies to Improve Treatment Efficiency. Cancers 2019, 11, 68. [Google Scholar] [CrossRef] [Green Version]
  32. Hoshyar, N.; Gray, S.; Han, H.; Bao, G. The effect of nanoparticle size on in vivo pharmacokinetics and cellular interaction. Nanomed. (Lond) 2016, 11, 673–692. [Google Scholar] [CrossRef] [Green Version]
  33. Yue, J.; Feliciano, T.J.; Li, W.; Lee, A.; Odom, T.W. Gold Nanoparticle Size and Shape Effects on Cellular Uptake and Intracellular Distribution of siRNA Nanoconstructs. Bioconjug Chem. 2017, 28, 1791–1800. [Google Scholar] [CrossRef]
  34. Sato, K.; Hosokawa, K.; Maeda, M. Rapid aggregation of gold nanoparticles induced by non-cross-linking DNA hybridization. J. Am. Chem. Soc. 2003, 125, 8102–8103. [Google Scholar] [CrossRef]
  35. Haiss, W.; Thanh, N.T.; Aveyard, J.; Fernig, D.G. Determination of size and concentration of gold nanoparticles from UV-vis spectra. Anal. Chem. 2007, 79, 4215–4221. [Google Scholar] [CrossRef]
  36. Aljabali, A.A.A.; Akkam, Y.; Al Zoubi, M.S.; Al-Batayneh, K.M.; Al-Trad, B.; Abo Alrob, O.; Alkilany, A.M.; Benamara, M.; Evans, D.J. Synthesis of Gold Nanoparticles Using Leaf Extract of Ziziphus zizyphus and their Antimicrobial Activity. Nanomaterials 2018, 8, 174. [Google Scholar] [CrossRef] [Green Version]
  37. Villena, J.A. New insights into PGC-1 coactivators: Redefining their role in the regulation of mitochondrial function and beyond. Febs J. 2015, 282, 647–672. [Google Scholar] [CrossRef] [PubMed]
  38. Aminabad, N.S.; Farshbaf, M.; Akbarzadeh, A. Recent Advances of Gold Nanoparticles in Biomedical Applications: State of the Art. Cell Biochem. Biophys. 2019, 77, 123–137. [Google Scholar] [CrossRef] [PubMed]
  39. Du, Y.; Xia, L.; Jo, A.; Davis, R.M.; Bissel, P.; Ehrich, M.F.; Kingston, D.G.I. Synthesis and Evaluation of Doxorubicin-Loaded Gold Nanoparticles for Tumor-Targeted Drug Delivery. Bioconjug Chem. 2018, 29, 420–430. [Google Scholar] [CrossRef] [PubMed]
  40. Fratoddi, I.; Benassi, L.; Botti, E.; Vaschieri, C.; Venditti, I.; Bessar, H.; Samir, M.A.; Azzoni, P.; Magnoni, C.; Costanzo, A.; et al. Effects of topical methotrexate loaded gold nanoparticle in cutaneous inflammatory mouse model. Nanomedicine 2019, 17, 276–286. [Google Scholar] [CrossRef] [PubMed]
  41. Wang, J.; Lu, Z.; Tang, H.; Wu, L.; Wang, Z.; Wu, M.; Yi, X.; Wang, J. Multiplexed Electrochemical Detection of MiRNAs from Sera of Glioma Patients at Different Stages via the Novel Conjugates of Conducting Magnetic Microbeads and Diblock Oligonucleotide-Modified Gold Nanoparticles. Anal. Chem. 2017, 89, 10834–10840. [Google Scholar] [CrossRef]
  42. Gupta, R.; Kashyap, N.; Rai, B. Transdermal cellular membrane penetration of proteins with gold nanoparticles: A molecular dynamics study. Phys. Chem. Chem. Phys. 2017, 19, 7537–7545. [Google Scholar] [CrossRef]
  43. Carabineiro, S.A.C. Applications of Gold Nanoparticles in Nanomedicine: Recent Advances in Vaccines. Molecules 2017, 22, 857. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  44. Huo, S.; Chen, S.; Gong, N.; Liu, J.; Li, X.; Zhao, Y.; Liang, X.-J. Ultrasmall Gold Nanoparticles Behavior in Vivo Modulated by Surface Polyethylene Glycol (PEG) Grafting. Bioconjugate Chem. 2017, 28, 239–243. [Google Scholar] [CrossRef]
  45. Zong, J.; Cobb, S.L.; Cameron, N.R. Peptide-functionalized gold nanoparticles: Versatile biomaterials for diagnostic and therapeutic applications. Biomater. Sci. 2017, 5, 872–886. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  46. Emami, F.; Banstola, A.; Vatanara, A.; Lee, S.; Kim, J.O.; Jeong, J.H.; Yook, S. Doxorubicin and Anti-PD-L1 Antibody Conjugated Gold Nanoparticles for Colorectal Cancer Photochemotherapy. Mol. Pharm. 2019, 16, 1184–1199. [Google Scholar] [CrossRef] [PubMed]
  47. Peng, L.; Liang, Y.; Zhong, X.; Liang, Z.; Tian, Y.; Li, S.; Liang, J.; Wang, R.; Zhong, Y.; Shi, Y.; et al. Aptamer-Conjugated Gold Nanoparticles Targeting Epidermal Growth Factor Receptor Variant III for the Treatment of Glioblastoma. Int. J. Nanomed. 2020, 15, 1363–1372. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  48. Liu, J.; Lu, Y. Preparation of aptamer-linked gold nanoparticle purple aggregates for colorimetric sensing of analytes. Nat. Protoc. 2006, 1, 246–252. [Google Scholar] [CrossRef]
  49. Kim, D.; Jeong, Y.Y.; Jon, S. A drug-loaded aptamer-gold nanoparticle bioconjugate for combined CT imaging and therapy of prostate cancer. Acs Nano 2010, 4, 3689–3696. [Google Scholar] [CrossRef]
  50. Guo, Y.; Li, S.; Liu, J.; Yang, G.; Sun, Z.; Wan, J. Double functional aptamer switch probes based on gold nanorods for intracellular ATP detection and targeted drugs transportation. Sens. Actuators B Chem. 2016, 235, 655–662. [Google Scholar] [CrossRef]
  51. Amina, S.J.; Guo, B. A Review on the Synthesis and Functionalization of Gold Nanoparticles as a Drug Delivery Vehicle. Int. J. Nanomed. 2020, 15, 9823–9857. [Google Scholar] [CrossRef] [PubMed]
  52. Ramalingam, V.; Varunkumar, K.; Ravikumar, V.; Rajaram, R. Target delivery of doxorubicin tethered with PVP stabilized gold nanoparticles for effective treatment of lung cancer. Sci. Rep. 2018, 8, 3815. [Google Scholar] [CrossRef]
  53. Dreaden, E.C.; Austin, L.A.; Mackey, M.A.; El-Sayed, M.A. Size matters: Gold nanoparticles in targeted cancer drug delivery. Deliv 2012, 3, 457–478. [Google Scholar] [CrossRef] [Green Version]
  54. Zhang, C.; Zhang, F.; Han, M.; Wang, X.; Du, J.; Zhang, H.; Li, W. Co-delivery of 5-fluorodeoxyuridine and doxorubicin via gold nanoparticle equipped with affibody-DNA hybrid strands for targeted synergistic chemotherapy of HER2 overexpressing breast cancer. Sci. Rep. 2020, 10, 22015. [Google Scholar] [CrossRef] [PubMed]
  55. Fu, Z.; Xiang, J. Aptamer-Functionalized Nanoparticles in Targeted Delivery and Cancer Therapy. Int. J. Mol. Sci. 2020, 21, 9123. [Google Scholar] [CrossRef] [PubMed]
  56. Mashreghi, M.; Zamani, P.; Moosavian, S.A.; Jaafari, M.R. Anti-Epcam Aptamer (Syl3c)-Functionalized Liposome for Targeted Delivery Of Doxorubicin: In Vitro And In Vivo Antitumor Studies in Mice Bearing C26 Colon Carcinoma. Nanoscale Res. Lett. 2020, 15, 101. [Google Scholar] [CrossRef]
  57. Moosavian, S.A.; Abnous, K.; Akhtari, J.; Arabi, L.; Gholamzade Dewin, A.; Jafari, M. 5TR1 aptamer-PEGylated liposomal doxorubicin enhances cellular uptake and suppresses tumour growth by targeting MUC1 on the surface of cancer cells. Artif Cells Nanomed Biotechnol. 2018, 46, 2054–2065. [Google Scholar] [CrossRef]
  58. Song, Y.; Zhu, Z.; An, Y.; Zhang, W.; Zhang, H.; Liu, D.; Yu, C.; Duan, W.; Yang, C.J. Selection of DNA aptamers against epithelial cell adhesion molecule for cancer cell imaging and circulating tumor cell capture. Anal. Chem. 2013, 85, 4141–4149. [Google Scholar] [CrossRef] [PubMed]
  59. Nabavinia, M.S.; Gholoobi, A.; Charbgoo, F.; Nabavinia, M.; Ramezani, M.; Abnous, K. Anti-MUC1 aptamer: A potential opportunity for cancer treatment. Med. Res. Rev. 2017, 37, 1518–1539. [Google Scholar] [CrossRef]
  60. Takemura, K.; Wang, P.; Vorberg, I.; Surewicz, W.; Priola, S.A.; Kanthasamy, A.; Pottathil, R.; Chen, S.G.; Sreevatsan, S. DNA aptamers that bind to PrP(C) and not PrP(Sc) show sequence and structure specificity. Exp. Biol. Med. (Maywood) 2006, 231, 204–214. [Google Scholar] [CrossRef] [PubMed]
  61. Du, Y.Q.; Yang, X.X.; Li, W.L.; Wang, J.; Huang, C.Z. A cancer-targeted drug delivery system developed with gold nanoparticle mediated DNA–doxorubicin conjugates. Rsc Adv. 2014, 4, 34830–34835. [Google Scholar] [CrossRef]
  62. Shiao, Y.S.; Chiu, H.H.; Wu, P.H.; Huang, Y.F. Aptamer-functionalized gold nanoparticles as photoresponsive nanoplatform for co-drug delivery. Acs Appl. Mater. Interfaces 2014, 6, 21832–21841. [Google Scholar] [CrossRef]
  63. Yang, S.; Ren, Z.; Chen, M.; Wang, Y.; You, B.; Chen, W.; Qu, C.; Liu, Y.; Zhang, X. Nucleolin-Targeting AS1411-Aptamer-Modified Graft Polymeric Micelle with Dual pH/Redox Sensitivity Designed To Enhance Tumor Therapy through the Codelivery of Doxorubicin/TLR4 siRNA and Suppression of Invasion. Mol. Pharm. 2018, 15, 314–325. [Google Scholar] [CrossRef] [PubMed]
  64. Goncalves, A.S.C.; Rodrigues, C.F.; Moreira, A.F.; Correia, I.J. Strategies to improve the photothermal capacity of gold-based nanomedicines. Acta Biomater. 2020, 116, 105–137. [Google Scholar] [CrossRef]
  65. Elahi, N.; Kamali, M.; Baghersad, M.H. Recent biomedical applications of gold nanoparticles: A review. Talanta 2018, 184, 537–556. [Google Scholar] [CrossRef] [PubMed]
  66. Adewale, O.B.; Davids, H.; Cairncross, L.; Roux, S. Toxicological Behavior of Gold Nanoparticles on Various Models: Influence of Physicochemical Properties and Other Factors. Int. J. Toxicol. 2019, 38, 357–384. [Google Scholar] [CrossRef]
  67. Jia, Y.-P.; Ma, B.-Y.; Wei, X.-W.; Qian, Z.-Y. The in vitro and in vivo toxicity of gold nanoparticles. Chin. Chem. Lett. 2017, 28, 691–702. [Google Scholar] [CrossRef]
  68. Cho, W.S.; Cho, M.; Jeong, J.; Choi, M.; Cho, H.Y.; Han, B.S.; Kim, S.H.; Kim, H.O.; Lim, Y.T.; Chung, B.H.; et al. Acute toxicity and pharmacokinetics of 13 nm-sized PEG-coated gold nanoparticles. Toxicol. Appl. Pharm. 2009, 236, 16–24. [Google Scholar] [CrossRef]
  69. Patlolla, A.K.; Kumari, S.A.; Tchounwou, P.B. A comparison of poly-ethylene-glycol-coated and uncoated gold nanoparticle-mediated hepatotoxicity and oxidative stress in Sprague Dawley rats. Int. J. Nanomed. 2019, 14, 639–647. [Google Scholar] [CrossRef] [Green Version]
  70. Pong, B.-K.; Elim, H.I.; Chong, J.-X.; Ji, W.; Trout, B.L.; Lee, J.-Y. New Insights on the Nanoparticle Growth Mechanism in the Citrate Reduction of Gold(III) Salt:  Formation of the Au Nanowire Intermediate and Its Nonlinear Optical Properties. J. Phys. Chem. C 2007, 111, 6281–6287. [Google Scholar] [CrossRef]
Ijms 22 01976 g001 550
Figure 1. Synthesis and characterization of PrPC-Apt-functionalized doxorubicin-oligomer-AuNPs (PrPC-Apt DOA). (A) Schematic diagram of PrPC-Apt DOA. (B) UV-Vis spectra of AuNPs at each experimental step (n = 3). (C) dynamic light scattering (DLS) measurements for the hydrodynamic radius of PrPC-Apt DOA at each experimental step (n = 3). (D) Fluorescence measurement for the binding ratios of Dox to cDL-DNA, cDL-DNA/PrPC-Apt, and cDL-DNA/PrPC-Apt/AuNPs (n = 3).
Figure 1. Synthesis and characterization of PrPC-Apt-functionalized doxorubicin-oligomer-AuNPs (PrPC-Apt DOA). (A) Schematic diagram of PrPC-Apt DOA. (B) UV-Vis spectra of AuNPs at each experimental step (n = 3). (C) dynamic light scattering (DLS) measurements for the hydrodynamic radius of PrPC-Apt DOA at each experimental step (n = 3). (D) Fluorescence measurement for the binding ratios of Dox to cDL-DNA, cDL-DNA/PrPC-Apt, and cDL-DNA/PrPC-Apt/AuNPs (n = 3).
Ijms 22 01976 g001
Ijms 22 01976 g002 550
Figure 2. PrPC targeting of PrPC-Apt DOA. (A) Expression levels of PrPC were determined in PrPC-negative and PrPC-positive cells (n = 3). (B,C) Cellular uptake of PrPC-Apt DOA in PrPC-negative and PrPC-positive cells were determined by using flow cytometry (B) and fluorescence microscopy (C) (n = 3). Values represent mean ± SEM. ** p < 0.01 vs. PrPC-negative.
Figure 2. PrPC targeting of PrPC-Apt DOA. (A) Expression levels of PrPC were determined in PrPC-negative and PrPC-positive cells (n = 3). (B,C) Cellular uptake of PrPC-Apt DOA in PrPC-negative and PrPC-positive cells were determined by using flow cytometry (B) and fluorescence microscopy (C) (n = 3). Values represent mean ± SEM. ** p < 0.01 vs. PrPC-negative.
Ijms 22 01976 g002
Ijms 22 01976 g003 550
Figure 3. PrPC-Apt DOA induce more Reactive Oxygen Species (ROS) generation in colorectal cancer CRC cells than free Dox. (A) Catalase activity (n = 3) and (B) Superoxide Dismutase (SOD) activity (n = 3) in SNU-C5 cells post treatment with free Dox and PrPC-Apt DOA. (C) dihydroethidium (DHE) staining of SNU-C5 cells, as measured using flow cytometry (n = 3). The percentages of DHE-positive cells are shown in the graph. Values represent mean ± SEM (n = 3). * p < 0.05, ** p < 0.01, *** p < 0.001 vs. control; ## p < 0.05 vs. free Dox.
Figure 3. PrPC-Apt DOA induce more Reactive Oxygen Species (ROS) generation in colorectal cancer CRC cells than free Dox. (A) Catalase activity (n = 3) and (B) Superoxide Dismutase (SOD) activity (n = 3) in SNU-C5 cells post treatment with free Dox and PrPC-Apt DOA. (C) dihydroethidium (DHE) staining of SNU-C5 cells, as measured using flow cytometry (n = 3). The percentages of DHE-positive cells are shown in the graph. Values represent mean ± SEM (n = 3). * p < 0.05, ** p < 0.01, *** p < 0.001 vs. control; ## p < 0.05 vs. free Dox.
Ijms 22 01976 g003
Ijms 22 01976 g004 550
Figure 4. PrPC-Apt DOA reduce PGC-1α expression and mitochondrial membrane potential. (A) Expression levels of PGC-1α were determined post treatment of SNU-C5 cells with free Dox or PrPC-Apt DOA (n = 3). (B) Complex IV activity was analyzed post treatment of SNU-C5 cells with free Dox or PrPC-Apt DOA (n = 3). (C) The tetramethylrhodamine ethyl ester (TMRE)-positive population was quantified using flow cytometry analysis post treatment of SNU-C5 cells with free Dox or PrPC-Apt DOA (n = 3). Values represent mean ± SEM. * p < 0.05, ** p < 0.01, *** p < 0.001 vs. control; ## p < 0.01 vs. free Dox.
Figure 4. PrPC-Apt DOA reduce PGC-1α expression and mitochondrial membrane potential. (A) Expression levels of PGC-1α were determined post treatment of SNU-C5 cells with free Dox or PrPC-Apt DOA (n = 3). (B) Complex IV activity was analyzed post treatment of SNU-C5 cells with free Dox or PrPC-Apt DOA (n = 3). (C) The tetramethylrhodamine ethyl ester (TMRE)-positive population was quantified using flow cytometry analysis post treatment of SNU-C5 cells with free Dox or PrPC-Apt DOA (n = 3). Values represent mean ± SEM. * p < 0.05, ** p < 0.01, *** p < 0.001 vs. control; ## p < 0.01 vs. free Dox.
Ijms 22 01976 g004
Ijms 22 01976 g005 550
Figure 5. PrPC-Apt DOA inhibit mitochondrial function of CRC cells to a greater degree, as compared to free Dox. (A) Mitochondrial oxygen consumption rates (OCRs) of SNU-C5 cells treated with free Dox or PrPC-Apt DOA were measured over time (min). The cells were treated with oligomycin (1 μM, 20 min), FCCP (0.75 μM, 40 min), and antimycin A (1 μM, 60 min) to obtain bioenergetic parameters. (B) Basal respiration was measured by subtracting non-mitochondrial OCR (which is the remaining OCR post antimycin A treatment) from the initial OCR level. (C) Maximal respiration was measured upon addition of FCCP. (D) Proton leak was calculated by subtracting the OCR post antimycin A treatment from the OCR post oligomycin A treatment. (E) Adenosine triphosphate (ATP) production was determined by subtracting non-mitochondrial OCR from the OCR value of basal respiration. The histogram shows representative data from one replicate experiment (n = 5). The values represent mean ± SEM. ** p < 0.01 vs. control; # p < 0.05, ## p < 0.01 vs. free Dox.
Figure 5. PrPC-Apt DOA inhibit mitochondrial function of CRC cells to a greater degree, as compared to free Dox. (A) Mitochondrial oxygen consumption rates (OCRs) of SNU-C5 cells treated with free Dox or PrPC-Apt DOA were measured over time (min). The cells were treated with oligomycin (1 μM, 20 min), FCCP (0.75 μM, 40 min), and antimycin A (1 μM, 60 min) to obtain bioenergetic parameters. (B) Basal respiration was measured by subtracting non-mitochondrial OCR (which is the remaining OCR post antimycin A treatment) from the initial OCR level. (C) Maximal respiration was measured upon addition of FCCP. (D) Proton leak was calculated by subtracting the OCR post antimycin A treatment from the OCR post oligomycin A treatment. (E) Adenosine triphosphate (ATP) production was determined by subtracting non-mitochondrial OCR from the OCR value of basal respiration. The histogram shows representative data from one replicate experiment (n = 5). The values represent mean ± SEM. ** p < 0.01 vs. control; # p < 0.05, ## p < 0.01 vs. free Dox.
Ijms 22 01976 g005
Ijms 22 01976 g006 550
Figure 6. PrPC-Apt DOA efficiently inhibit the proliferation of CRC cells to a greater extent than free Dox. (A) Cell cycle analysis of SNU-C5 cells post treatment with free Dox and PrPC-Apt DOA (n = 3). (B) Western blot analysis of SNU-C5 cells for CDK2, cyclin E, CDK4, and cyclin D1 post treatment with free Dox and PrPC-Apt DOA (n = 3). Protein levels were determined using densitometry relative to β-actin. The values represent mean ± SEM. * p < 0.05, ** p < 0.01, *** p < 0.001 vs. control; # p < 0.05, ## p < 0.01 vs. free Dox.
Figure 6. PrPC-Apt DOA efficiently inhibit the proliferation of CRC cells to a greater extent than free Dox. (A) Cell cycle analysis of SNU-C5 cells post treatment with free Dox and PrPC-Apt DOA (n = 3). (B) Western blot analysis of SNU-C5 cells for CDK2, cyclin E, CDK4, and cyclin D1 post treatment with free Dox and PrPC-Apt DOA (n = 3). Protein levels were determined using densitometry relative to β-actin. The values represent mean ± SEM. * p < 0.05, ** p < 0.01, *** p < 0.001 vs. control; # p < 0.05, ## p < 0.01 vs. free Dox.
Ijms 22 01976 g006
Ijms 22 01976 g007 550
Figure 7. PrPC-Apt DOA efficiently promote the apoptosis of CRC cells. (A) Live and dead cells assay in SNU-C5 cells post treatment with free Dox and PrPC-Apt DOA. (B) Annexin V/PI staining of SNU-C5 cells post treatment with free Dox and PrPC-Apt DOA. (C) Western blot analysis of apoptosis-related proteins in SNU-C5 cells post treatment with free Dox and PrPC-Apt DOA. The values represent mean ± SEM. * p < 0.05, ** p < 0.01, *** p < 0.001 vs. control; # p < 0.05, ## p < 0.01, ### p < 0.001 vs. free Dox.
Figure 7. PrPC-Apt DOA efficiently promote the apoptosis of CRC cells. (A) Live and dead cells assay in SNU-C5 cells post treatment with free Dox and PrPC-Apt DOA. (B) Annexin V/PI staining of SNU-C5 cells post treatment with free Dox and PrPC-Apt DOA. (C) Western blot analysis of apoptosis-related proteins in SNU-C5 cells post treatment with free Dox and PrPC-Apt DOA. The values represent mean ± SEM. * p < 0.05, ** p < 0.01, *** p < 0.001 vs. control; # p < 0.05, ## p < 0.01, ### p < 0.001 vs. free Dox.
Ijms 22 01976 g007
Ijms 22 01976 g008 550
Figure 8. PrPC-Apt DOA efficiently inhibit the sphere formation capacity of CRC cells. (A) Sphere formation assay of SNU-C5 cells post treatment with free Dox or PrPC-Apt DOA (n = 3). Scale bar: 200 μm. (B) Diameters of the spheroids are shown in the graph. Dot symbols represent individual values. The values represent mean ± SEM. * p < 0.05, ** p < 0.01 vs. control; # p < 0.05 vs. free Dox.
Figure 8. PrPC-Apt DOA efficiently inhibit the sphere formation capacity of CRC cells. (A) Sphere formation assay of SNU-C5 cells post treatment with free Dox or PrPC-Apt DOA (n = 3). Scale bar: 200 μm. (B) Diameters of the spheroids are shown in the graph. Dot symbols represent individual values. The values represent mean ± SEM. * p < 0.05, ** p < 0.01 vs. control; # p < 0.05 vs. free Dox.
Ijms 22 01976 g008
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Go, G.; Lee, C.-S.; Yoon, Y.M.; Lim, J.H.; Kim, T.H.; Lee, S.H. PrPC Aptamer Conjugated–Gold Nanoparticles for Targeted Delivery of Doxorubicin to Colorectal Cancer Cells. Int. J. Mol. Sci. 2021, 22, 1976. https://0-doi-org.brum.beds.ac.uk/10.3390/ijms22041976

AMA Style

Go G, Lee C-S, Yoon YM, Lim JH, Kim TH, Lee SH. PrPC Aptamer Conjugated–Gold Nanoparticles for Targeted Delivery of Doxorubicin to Colorectal Cancer Cells. International Journal of Molecular Sciences. 2021; 22(4):1976. https://0-doi-org.brum.beds.ac.uk/10.3390/ijms22041976

Chicago/Turabian Style

Go, Gyeongyun, Chang-Seuk Lee, Yeo Min Yoon, Ji Ho Lim, Tae Hyun Kim, and Sang Hun Lee. 2021. "PrPC Aptamer Conjugated–Gold Nanoparticles for Targeted Delivery of Doxorubicin to Colorectal Cancer Cells" International Journal of Molecular Sciences 22, no. 4: 1976. https://0-doi-org.brum.beds.ac.uk/10.3390/ijms22041976

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop