Siddhi Bagwe-Parab
Pratik Yadav
Ginpreet Kaur
Hardeep Singh Tuli
Harpal Singh Buttar- 1Shobhaben Pratapbhai Patel School of Pharmacy and Technology Management, Shri Vile Parle Kelavani Mandals Narsee Monjee Institute of Management Studies, Mumbai, India
- 2Department of Biotechnology, Maharishi Markandeshwar (Deemed to be University), Mullana, Ambala, India
- 3Department of Pathology and Laboratory Medicine, Faculty of Medicine, University of Ottawa, Ottawa, ON, Canada
The incidence of gastrointestinal disorders (GID) and cancers is escalating all over the world. Limited consumption of colostrum by newborns not only weakens the immune system but also predisposes infants to microbial infections. Colostrum is nature’s perfect food, sometimes referred to as the ‘elixir of life’. Breast-fed infants have a lower incidence of GI tract infections than infants fed formula or cow’s milk. As per WHO statistics, cancer is the most prevalent disease globally and causes 9.6 million deaths worldwide. The current strategies for treating cancer include chemotherapy, radiation, and surgery. However, chemotherapy and radiation exposure are usually associated with serious long-term side effects and deterioration in the quality of life (QOL) of patients. Furthermore, the hospitalization and medication costs for treating cancers are exorbitant and impose high economic burden on healthcare systems. People are desperately looking for cost-effective and affordable alternative therapies for treating GID and cancers. Therefore, there is an urgent need for clinically evaluating the anticancer compounds isolated from plants and animals. Such therapies would not only be economical and have fewer side effects, but also help to improve the QOL of cancer patients. Recently, bovine colostrum (BC) has caught the attention of many investigators to explore its anticancer potential in humans. BC impregnated dressings are highly effective in treating chronic wounds and diabetic foot ulcer. BC is rich in lactoferrin, a glycoprotein with strong antioxidant, anti-inflammatory, anti-cancer, and anti-microbial properties. Intravaginal application of BC tablets is effective in causing the regression of low-grade cervical intraepithelial neoplasia. The underlying mechanisms of BC at cellular, genetic, and molecular levels remain to be ascertained. Oral BC supplement is well-tolerated, but some people may experience problems such as flatulence and nausea. Well-designed, randomized, placebo-controlled, clinical trials are needed to access the therapeutic potential, long-term safety, and optimal doses of BC products. This review is aimed to highlight the anticancer potential of BC and its components, and the therapeutic applications of BC supplements in treating gastrointestinal diseases in children and adults. We also discuss the health promotion benefits and therapeutic potential of BC nutraceuticals in reducing the incidence of non-communicable diseases.
Introduction
Role of Colostrum Against Gastrointestinal Disorders (GIDs)
Necrotizing enterocolitis and neonatal sepsis are the major gastrointestinal ailments in premature babies, newborns, and toddlers, especially those whose mothers are unable to provide colostrum. Breast-fed infants have a lower incidence of GI tract infections than infants fed with formula or cow’s milk. GIDs can lead to stunted physical growth and neurodevelopment, retarded immune function, malabsorption of nutrients, and susceptibility to other diseases like allergies and asthma at an early age. In newborns, colostrum acts as a broad-spectrum antibacterial agent that protects against gut infections as well as contributes to physical growth, immune function, and development of the GI tract. In adults, colostrum promotes healing of the GI tract and protects against gut pathogens (bacteria, viruses, fungi, yeast, mold, etc.), and leaky gut syndrome. Mother’s colostrum or first milk is significantly richer in biologically active peptides, anti-oxidants, anti-inflammation agents, and growth promoting factors that differ substantially from later milk (Bagwe et al., 2015; Buttar et al., 2017). According to Gensollen et al. (2016), some GIDs are caused by the compromised immune system in neonates. The intake of mother’s colostrum lays the foundation for life-long immunity. In some cases, the neonate’s immunity is compromised due to the lack of mother’s colostrum or breast-feeding difficulty (Le Doare et al., 2018). Consequently, GID problems arise during adolescence or adulthood due to a deficient immune system. It is therefore imperative for neonates to consume colostrum for physical growth and proper development of the immune system, and to curb GID disorders later in life.
It has been suggested that bovine colostrum (BC) contains almost ninety bioactive components. These bioactive substances consist of immunoglobulins and growth factors, antibodies, higher levels of amino acids, oligosaccharides, antimicrobial compounds, and immune regulators like lactoferrin (Jacqmin, 2000). BC is also rich in vitamins and minerals. Colostrum provides nutrients in a highly concentrated low-volume form to the newborn. Due to its laxative properties, colostrum assists in the passage of baby’s initial stools or meconium and helps to remove excess bilirubin from the infant’s body to prevent jaundice (Buttar et al., 2017). Excess accumulation of bilirubin in the neonate can cause jaundice, anemia, liver cirrhosis, and Gilbert’s syndrome (Maqbool, 1992; Crittenden et al., 2007; de Almeida and Draque, 2007). Research has shown that BC is 100-fold to 1,000-fold more potent than human colostrum. Thus, human infants can thrive very well by consuming infant- formula containing BC supplements that can provide passive immunity and growth factors needed for physical and gastrointestinal development. BC is an emerging nutraceutical and innovative therapeutic products being developed for children and adults.
Cancer
Cancer is the second leading cause of mortality and morbidity worldwide, behind only cardiovascular diseases (Siegel et al., 2016; Miller et al., 2019). Cancer is a collective name for a disease where the abnormal body cells divide in an uncontrollable fashion in a body part or organ, resulting in a tumor or carcinoma. Genetic, epigenetic, and environmental factors play an important role in the occurrence and progression of cancer. There are two types of cancer: benign or noninvasive and malignant or invasive. Malignant cancer cells can invade nearby tissues or organs and can also travel to distant places in the body through blood or the lymphatic system, and consequently form a new tumor far away from the original one. According to Seebacher et al. (2019), nearly 14.1 million people suffer from cancer, and about 9.6 million deaths were reported worldwide in 2018. From a mortality point of view, 1 out of 6 deaths are caused by cancer (Bray et al., 2018). The common types of cancers include: carcinoma, sarcoma, leukemia, lymphoma, melanoma, lung, colorectal, prostate, and breast cancer (Brandal and Heim, 2015; Linehan et al., 2016; Rosenberg et al., 2016; Tricoli et al., 2016; Bullinger et al., 2017; Etienne et al., 2017; Meurer et al., 2017; Rajyaguru et al., 2018; Miolo et al., 2019). The current strategies for cancer treatment consist of chemotherapy, radiotherapy, bone marrow transplants, and surgery. However, these therapies have drawbacks and limitations; for instance, radiation therapy causes indirect damage to surrounding tissues, and chemotherapy results in vital organ toxicity and also causes drug resistance, whereas surgical interventions may sometimes precipitate tumor recurrence (Formenti and Demaria, 2009; Taylor and Kirby, 2015; Vitetta et al., 2019). Recent trends in cancer treatment also include targeted drug delivery and immunotoxin therapy (Vitetta et al., 2019). Immunotoxin is a conjugated protein which blends a targeted conjugate with a toxin. These immunotoxins enter into the cancer cell through endocytosis and lead to cell death.
Stomach, colorectal, and lung cancer are common in both sexes, whereas liver and prostate cancer is common in men, and breast and cervical cancer occur in women. Currently, gastric cancer is one of the serious diseases worldwide. According to global cancer statistics data, gastric cancer is the fourth most common cancer worldwide. Serious vital organ deleterious effects happen when gastric cancer is treated by chemotherapy (Rugge et al., 2015; Rathe et al., 2019). Therefore, there is an urgent need for the development of less toxic therapeutic agents for the prevention and cure of stomach cancer (Farziyan et al., 2016).
Role of BC for the Treatment of Cancer and Gastrointestinal Diseases (GIDs)
Colostrum or first milk is secreted by all female mammals, including women, during the first four days after parturition and is provided to their neonates during the initial 24-48 hours after birth (Bagwe et al., 2015; Agarwal and Gupta, 2016; Hyrslova et al., 2016; Jolly and Mascaro, 2016; Buttar et al., 2017). Colostrum is thick, sticky, yellowish liquid which not only provides nutrition and immunity but also gives protection against microbial infections. Almost all essential nutrients such as protein, fat, lactose, lactoferrin, immunoglobulins, vitamins and minerals, and growth factors are present in the colostrum in significantly higher concentrations than the regular mature milk (Shah, 2000). Colostrum creates life-long immunity in the newborn and helps in maturing the GI tract of babies. Whereas in adults, colostrum promotes healing of the GI tract and protects against gut pathogens (bacteria, viruses, fungi, yeast, mold, etc.), and leaky gut syndrome (Shah, 2000; Hurley and Theil, 2011; Osada et al., 2014; Wu Xiaoyun and Xiong Lin, 2015). The major bioactive components of bovine colostrum and their functions in children and adults are summarized in Table 1. BC acquired from cows and buffalo possess more immunoglobulins than human colostrum, and human infants could benefit by consuming BC (Ulfman et al., 2018). BC is usually regarded as safe in humans, whereas some people may experience nausea and flatulence initially, which declines over time. BC should not be given to individuals allergic to milk and milk products.
Table 1 Composition of bovine colostrum and functions in children and adults.
The central theme of this review is to address the potential benefits of colostrum nutrients in children and adults as well as the usefulness of BC components for the treatment of cancer and gastrointestinal disorders. As discussed earlier, the conventional cancer therapies include chemotherapy, radiotherapy, bone marrow transplant, and surgical interventions, but these therapies have drawbacks and limitations. Hence there is a need for cost-effective and safe novel therapies for the treatment of cancer. Limited numbers of clinical trials with BC have shown anticancer effects in different cancer types (Layman et al., 2018; França-Botelho, 2019). The anticancer effects of lactoferrin, proline rich polypeptides, conjugated linolenic acid (CLA), and alpha-lactalbumin are presented in Table 2. The nutrient profile of BC is markedly different from mature milk. The quantitative concentrations of the main constituents of cow colostrum and cow milk are depicted in Table 3. It can be seen from Table 4 that the concentrations of lactoferrin, IgA, insulin like growth factor, growth hormone, and epidermal growth factor are markedly higher in human colostrum as opposed to bovine colostrum (Godhia and Patel, 2013, Bagwe et al., 2015).
Table 2 Important components of bovine colostrum: Functions and anticancer effects.
Table 3 Main components of bovine colostrum and bovine milk: Amounts represented as per liter.
Table 4 Comparison of human colostrum and bovine colostrum.
Role of Human and Bovine Colostrum in the Maturation of GI Tract in Babies
Many researchers have shown that colostrum plays a critically significant role in the growth and maturity of the GI tract in infants. The nutrients in colostrum create a suitable environment - namely biochemical, physiological, morphological, functional, immunological, and antimicrobial - for the maturity of the gastrointestinal tract in new-born babies (Pluske, 2016). Recent studies performed on piglets, serving as a model for human infants, have suggested that the epidermal growth factor of BC is responsible for the growth and maturity of the GI tract in infants (Bedford et al., 2015). Another study in piglets also demonstrated the growth promoting effects of bovine lactoferrin in the stimulation of intestinal cell proliferation, increased crypt depth, and villus length. Lactoferrin is a glycoprotein with strong antioxidant, anti-inflammation, anti-cancer, and anti-microbial properties. Lactoferrin induces the stimulation of T-helper-1/T-helper-2 cytokine immune response and secretion of anti-inflammatory cytokines. It has been observed that lactoferrin can prevent gastric infections, necrotizing enterocolitis and late onset sepsis in children (Pammi and Abrams, 2015; Donovan, 2016; Pieper et al., 2016).
Application of BC in Treating Inflammatory Bowel Disease (IBD) and Nonalcoholic Steatohepatitis (NASH)
Inflammatory bowel diseases (IBDs) result from alterations in the systemic immune response and modulation of the gut immune system, which induce inflammation-mediated damage to the gastro-intestinal tract and injury to related organs. BC supplements have been used as an alternative therapy for the treatment of nonalcoholic steatohepatitis (NASH) and insulin resistance type 2 diabetes and colitis. Hyperimmune bovine colostrum is enriched with IgG and enhanced with glycosphingolipid immune adjuvants and anti-lipopolysaccharides. To determine the safety and efficacy of hyperimmune bovine colostrum (Imm124-E), Mizrahi et al. (2012) performed an open-label trial in ten patients diagnosed with insulin resistant type 2 diabetes and nonalcoholic steatohepatitis (NASH). Oral administration of Imm124-E at doses of 600 mg thrice daily (1800 mg/day) for 30 days improved type 2 diabetes and hyperlipidemia, and alleviated NASH through immunomodulatory action without any adverse effects. Oral administration of Imm124-E to mice ameliorated immune-mediated colitis induced by intra-colonic instillation of trinitrobenzene sulfonate. Imm124-E improved bowel histology and regeneration score, and decreased the extent of colitis damage in mice. This pathophysiological improvement was associated with the elevation of serum IL10, anti-inflammatory cytokine levels, CD4+, CD25+, and CD4+ Foxp3+ Tregs (Ya’acov et al., 2015). According to Ilan (2016), oral immune modulation therapies (e.g. nutraceuticals, functional foods, probiotics, prebiotics, polyunsaturated fatty acids, polyphenols, non-absorbable gut-associated adjuvuants, etc.) may be helpful to re-establish gut tolerance and to alter the gut immune system via the modulation of intestinal microbiota to treat autoimmune and inflammatory disorders like IBD.
Application of BC Supplements in Treating Crohn’s Disease and Gut Infections
Colostrum may be beneficial in chronic inflammatory diseases, such as various forms of arthritis, Crohn’s disease, or inflammatory bowel disease (IBD). Crohn’s or Celiac disease is an inflammatory bowel disease that causes abdominal pain and diarrhea (Sequeira et al., 2014). Non-steroidal anti-inflammatory drugs (NSAIDS) are often prescribed to reduce pain and abdominal cramps. However, chronic use of NSAIDS can cause peptic ulcers and alterations of gut microbiota, and the latter may induce leaky gut syndrome. BC possesses strong anti-inflammatory and anti-bacterial effects and can neutralize the lipopolysaccharides produced by gram negative bacteria (Rawal et al., 2008). BC reduces the expression of TNF-α in Caco-2 and HT29 cell lines as well as inhibits IL-8 expression and production of inflammatory cytokines, and consequently reduces gut inflammation. BC also decreases the adherence of invasive E. coli bacteria in human cell lines (Chae et al., 2017). Collectively, these findings suggest the promising therapeutic potential of BC in treating GI tract infections and inflammation-related IBD. Results of clinical and preclinical studies done with BC and dosage forms used for curing internal pathologies and external wounds are shown in Table 5.
Table 5 Colostrum dosage forms used for treating internal pathologies and external wounds.
Role of BC and Components in Treating Gut Diseases Caused by Microbial Infections
Generally, acute infectious diarrhea, immunodeficiency diarrhea, short bowel syndrome, IBD, etc. are treated with synthetic pharmaceuticals (Holtmann et al., 2017). The secondary infections in the GI tract and diarrhea in AIDS patients are also treated with drugs (Playford et al., 1999). A limited number of randomized, double-blind, and controlled studied have been done in children and adults to evaluate the efficacy of BC supplements for treating gut diseases caused by microbial infections. BC and its components were found to be effective against Gram negative and Gram positive bacteria and helped in treating gut infections and diarrhea. The dosages of BC supplements and bioactive ingredients used in preclinical and clinical studies for treating gastrointestinal diseases are summarized in Table 6.
Table 6 Pre-clinical and clinical applications of bovine colostrum in gastrointestinal diseases.
Role of Lactoferrin and Lactalbumin in Cancer Therapy
Lactoferrin (LF) is an excellent immune modulator and anticancer agent and has a tissue regenerative capacity. It can also inhibit the production of inflammatory cytokines. Lactalbumin is present in whey and can markedly improve the immune response and enhance the synthesis of glutathione. It has been observed that lactoferrin and lactalbumin can induce apoptosis in cancerous cells (Teixeira et al., 2019). LF has been reported to elevate the level of caspase-1 and IL-18, and in turn reduce the metastatic foci in the intestine. LF-induced apoptotic activity of cytotoxic T and natural killer (NK) cells has also been observed. In addition, LF inhibits hepatic CYP1A2 enzyme, which is responsible for the activation of carcinogens (Tsuda et al., 2006). LF may be employed as a carrier for chemotherapeutic agents, especially for the treatment of brain tumors, due to its ability to cross the blood-brain barrier (Cutone et al. (2020). It therefore appears that LF and whey lactalbumin can be used as combination adjunct therapies with chemo- and radiotherapy for treating cancer. This approach would not only enhance the chemotherapeutic effectiveness of drugs, but also limit the use of chemo- and radiotherapy, resulting in reduced incidences of undesirable side effects observed in cancer patients.
In Vitro Evaluation of the Anticancer Effects of BC Components Using Different Human Cancer Cell Lines
In vitro cell culture studies are used in selected cancer cell lines as a promising tool to determine the antiproliferative and cytotoxic effects of potential anticancer agents isolated from natural sources or synthesized in the laboratory. In vitro cell culture studies provide clues about the mechanism of action of anticancer agents toward cancer cells. Anti-cancer effects of lactoferrin were evaluated using MTT assay. The addition of lactoferrin in the culture medium inhibited the growth of cancer cell lines (MDA-MB-231 and MCF-7) (Sharma et al., 2019). Purified lactoferrin (2 mg/ml) retarded the growth of esophageal cancer cell lines (KYSE-30) and HEK cancer cell lines. The addition of 500 µg/ml of lactoferrin in the culture medium decreased the cell viability of KYSE-30 cancer cells by 80% after 62 hours’ exposure. No effect was noted in the normal HEK cell line. Flow cytometry analysis suggested that lactoferrin induced apoptosis in KYSE-30 human esophagus cancer cell lines (Farziyan et al., 2016). The results of in vitro studies done to assess the anticancer properties of BC components (lactoferrin, liposomal bovine lactoferrin, bovine lactoperoxidase, lactoferrin nanoparticles, and conjugated linolenic acid) on different cancer cell lines (e.g., gastric, esophagus, colorectal, liver, lung, prostate, breast, ovarian) are summarized in Table 7.
Table 7 Anticancer effects of bovine colostrum components on different cancer cell lines.
In Vivo Anticancer Effects of BC Components in Animal Models and Humans
Following the information obtained from in vitro studies, the next step involves preclinical investigations in appropriate animal models to assess the safety, efficacy, and toxicity of anticancer agents. Numerous anticancer studies with BC supplements and major components have been done on rodents. For instance, lactoferrin and conjugated linolenic acid (CLA) have been tested for treating colorectal, lung, and esophageal cancers in rats and mice. Reduction in colon tumor load and downregulation (Figure 1) in the expression of VEGF were observed in the preclinical studies (Tung et al., 2013; Sugihara et al., 2017). A limited number of clinical trials in a small number of patients have been performed in humans to understand the anticancer potential of BC components. Based on the promising anticancer effects of CLA in preclinical models, an open-label clinical study was done on 24 women diagnosed with breast cancer. CLA was given orally at doses of 7.5 G/day for 20 days. CLA was found to suppress the expression of fatty acid synthase (FASN) and lipoprotein lipase (LPL). The depressed activity of these biomarker enzymes indicates the suppression of breast tumor growth (McGowan et al., 2013). The results of another clinical trial suggested that CLA (3G/day) may be useful in rectal cancer patients undergoing chemoradiotherapy (Mohammadzadeh et al., 2013). The information obtained from preclinical and clinical effects of lactoferrin, liposomal lactoferrin, and CLA in different types of cancers is shown in Table 8.
Figure 1 A normal cell mutates into the cancer cell, which divides enormously and spreads across the surrounding tissues. The pathways responsible for initiation and metastasis of cancer and the role of bovine colostrum (BC) on the amelioration of the same is given as follows. (A) Azoxymethane is responsible for tumor multiplication and cancer cell development. BC inhibits the development if azoxymethane (AOM)-induced aberrant crypt foci (ACF), therefore reducing the cell viability. (B) BC inhibits the proliferation of tumor angiogenesis by dimethylhydrazine. (C) Nuclear factor-κB (NF-κB) is the transcription factor that is responsible for cancer cell growth, tumor formation, and tumor cell proliferation, and prevents tumor cells from apoptosis. BC suppresses NF-κB expression approximately by 10-fold. (D) E2F2 factor plays an important role in the tumorigenesis of the cancerous cells. BC inhibits expression of E2F2 factor and initiates cell cycle arrest. (E) BC inhibits the enzymes fatty acid synthetase (FAS) and lipoprotein lipase (LPL), which in turn inhibit neoplastic lipogenesis. (F) Matrix metalloproteinaise 2/9 (MMP-2/9) allows cancer cells to migrate out of the primary tumor to form metastases. BC supresses the levels of the MMP- 2/9. (G) BC inhibits the expression of Human Vascular Endothelial Growth Factor (hVEGF), which is responsible for proliferation of the cancer cells. AOM, Azoxymethane; ACF, Azoxymethane induced aberrant crypt foci; NF-κB, Nuclear factor Kappa B; E2Fi, E2F Transcription Factor 1; FAS, Fatty acid synthetase; LPL, Lipoprotein lipase; MMP, Matrix metalloproteinase; hVEGF, Human Vascular Endothelial Growth Factor.
Table 8 Preclinical and clinical effects of bovine colostrum components on different cancer types in animals and humans.
Intravaginal Application of BC Tablets Cause Spontaneous Regression Of HPV-Associated Low-Grade Cervical Intraepithelial Lesions in Women
Human papillomavirus (HPV) infection is the most common sexually transmitted disease in young people worldwide. Most infections are cleared by the immune system, but persistent infections may cause intraepithelial abnormalities in the infected cells that can develop into cancers of the cervix, vagina, vulva, anal canal, and penis. Immunotherapy is considered the most promising treatment for HPV-related pathologies. HPV vaccines have been developed to prevent HPV-associated cancer, external genital lesions, and genital warts (Bergman et al., 2019). In Italy, the immunomodulating action of BC was evaluated in an observational, multi-centre, pilot study, where 256 patients were enrolled with a history of low-grade cervical squamous intraepithelial lesions. At baseline, all patients were tested for cervical cytology (Pap smear), colposcopy, and targeted biopsy. BC-containing vaginal tablets (GINEDIER) were administered twice a week at bedtime for 24 weeks, without any other medication for the whole study period. The rates of regression were recorded histologically at the end of the study period. Overall regression rate with negative histology was 75.5% at the end of the 6 month follow-up period. The patients did not experience any adverse effects during the treatment. The authors concluded that, as opposed to a spontaneous regression period of 1-5 years, intravaginal topical application of BC significantly shortens the regression time of low-grade cervical intraepithelial lesions to half a year (Stefani et al., 2014).
Current and Future Developments of BC Nutraceuticals
In this review, we have attempted to summarize the nutraceutical health benefits of BC, and the therapeutic potential and effectiveness of marketed colostrum powder, capsules, and tablets for the treatment of various types of cancers and GI tract pathologies. BC is an emerging nutraceutical and innovative therapeutic products are being developed for children and adults. In future, BC products could be a boon in providing non-hazardous, cost-effective, and affordable alternative sources of natural remedies for treating different types of cancers, GIDs, and autoimmune disorders. However, there are several challenges and opportunities that need to be addressed. For instance, well-designed, placebo-controlled, and randomized clinical trials are needed to determine the long-term safety, effectiveness, and optimal doses of BC supplements. Some other aspects of BC nutraceuticals include the standardization of products originating from different breeds of cows and buffalo. In addition, good manufacturing practices and standardized techniques are required for making BC formulations, and possible adulteration of BC supplements with synthetic drugs and microbial contaminants, just to name a few. More basic research is needed to understand the mechanism of action of different components of BC for their anticancer and antidiabetic properties, and for curing wounds, gastrointestinal disorders, and inflammatory bowel diseases.
Nutraceuticals are defined as substances that provide physiological benefits and assist in improving overall health beyond basic nutritional functions and protect against non-communicable diseases. Generally, nutraceuticals consist of products isolated or purified from vegetables and fruits, colostrum supplements, and dairy products, and are sold as non-pharmacological, cost-effective, and affordable alternative therapies for the prevention and treatment of neurodegenerative and cardiovascular diseases, musculoskeletal abnormalities, diabetes, obesity, and some cancers. The influence of nutraceuticals, functional foods, natural health products, dietary supplements, and probiotics is often neglected by healthcare professionals and leading experts in the field of medicine. Nutraceuticals could be one of the biggest drivers for curing the global epidemic of chronic non-communicable diseases, including obesity, diabetes, cardiovascular diseases, and certain cancers. However, the evidence-based dietary advice is beset by poor quality science, a limited number of randomized, placebo-controlled studies, and unresolved controversy about the role of nutraceuticals in curing non-communicable diseases. Good manufacturing practices (GMPs) and high-quality control standards should be used for the manufacturing of BC nutraceuticals. Post-marketing surveillance should be conducted diligently for the tolerability of BC supplements and bioactive components. Dairy farmers should be encouraged to collect BC using sterile and hygienic conditions as much as possible.
Bovine colostrum is significantly rich in biologically active peptides, antioxidants, anti-inflammation agents, and growth promoting factors that differ substantially from later milk. The benefits of BC are well known in the health and disease of children and adults. As discussed earlier, BC is an emerging nutraceutical and innovative therapeutic products that is being developed for children’s formulas and for the treatment of non-communicable diseases. Hopefully, BC supplements will greatly contribute to curing different cancer types, diabetes, cardiovascular diseases, necrotizing enterocolitis, and inflammatory bowel disease or Crohn’s disease, and autoimmune disorders. Understanding the biological roles of different BC ingredients is a major challenge for nutritionists and dieticians, basic researchers, and physicians.
BC can also mitigate a wide variety of bacterial, viral, fungal, and parasitic infections. BC impregnated dressings are non-allergic, safe, and promote wound-healing. Such dressings may be used as an adjunct for the management of deep wounds and burns. BC is richer in immunoglobulins than human colostrum and can be used in the treatment of immunodeficiency diseases and infections along with conventional medicines (Bagwe et al., 2015; Buttar et al., 2017). Our studies indicated that BC possesses strong antimicrobial activity against both Gram-tive and Gram+tive strains. The minimal inhibitory concentration (MIC) of colostrum was found to be 100 µg/ml against E. coli, S. aureus, P. vulgaris, E. aerogenes, and S. typhi (Yadav et al., 2016). It is possible that BC might have viricidal effects against the COVID-19 virus. Lactoferrin especially is well known for its anti-inflammation and anti-microbial properties. This hypothetical idea may be worth pursuing!
Conclusions
BC supplements have proven useful in the management of GIDs, such as acute infectious diarrhea, Helicobacter pylori infections, irritable bowel syndrome, inflammatory bowel disease (IBD), and different types of human cancer cell lines (e.g. esophagus, colorectal, lung, breast and ovarian cancer). The components of BC, such as lactoferrin, CLA, and alpha-lactalbumin, are useful in treating GI-related disorders and some cancer types. The oral consumption of BC can boost the immune system and improve the inflammatory condition of patients suffering from gastrointestinal disorders.
BC possesses strong antibacterial, antiviral, and antifungal properties, and has also exhibited antitumor actions in a limited number of in vitro and in vivo studies. Several components of BC have shown apoptosis in cancer cells and suppression in the growth of tumors. Also, NK cells are inhibited after BC exposure. While BC products are well tolerated, some patients allergic to dairy products may experience undesirable side effects. Overall, BC supplements can be safely used for the treatment of GIDs, autoimmune disorders, and different cancers. The clinical interactions of BC, if any, with orally administered prescription or over-the-counter drugs should be explored regarding the bioavailability and pharmacokinetics, and the possibility of such an interaction should be monitored in patients using synthetic drugs for co-morbid conditions.
Author Contributions
GK, HS, and HT visualized the presented idea, contributed to manuscript writing, and supervised the project. SB-P and PY contributed to literature searches and to preparing the manuscript draft. GK and HS revised and approved the manuscript.
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Abbreviations
BC, Bovine colostrum; CLA, Conjugated linolenic acid; GID, Gastrointestinal disorders; GIT, Gastrointestinal tract; IBD, Inflammatory bowel disease; NASH, Non-Alcoholic Steato Hepatitis; NK, Natural killer; NSAIDS = Non-steroidal anti-inflammatory drugs.
References
Abu-Serie, M. M., El-Fakharany, E. M. (2017). Efficiency of novel nanocombinations of bovine milk proteins (lactoperoxidase and lactoferrin) for combating different human cancer cell lines. Sci. Rep. 7, 1–2. doi: 10.1038/s41598-017-16962-6
Agarwal, P., Gupta, R. (2016).A Review on Anticancer Property of Colostrum. Res. Rev. - J. Med. Heal. Sci. 5, 1–9.
Amiri, F., Moradian, F., Rafiei, A. (2015). Anticancer effect of lactoferrin on Gastric Cancer Cell Line AGS. rmm.mazums.ac.ir Res. Mol. Med. 3, 11. doi: 10.7508/rmm.2015.02.002
Arab, A., Akbarian, S., Ghiyasvand, R., Miraghajani, M. (2016). The effects of conjugated linoleic acids on breast cancer: A systematic review. Adv. Biomed. Res. 5, 115. doi: 10.4103/2277-9175.185573
Aunsholt, L., Jeppesen, P. B., Lund, P., Sangild, P. T., Ifaoui, I. B. R., Qvist, N., et al. (2014). Bovine colostrum to children with short bowel syndrome: a randomized, double-blind, crossover pilot study. JPEN J. Parenter. Enteral Nutr. 38, 99–106. doi: 10.1177/0148607112469630
Bagwe, S., Tharappel, L. J. P., Kaur, G., Buttar, H. S. (2015). Bovine colostrum: An emerging nutraceutical. J. Complement. Integr. Med. 12, 175–185. doi: 10.1515/jcim-2014-0039
Barakat, S. H., Meheissen, M. A., Omar, O. M., Elbana, D. A. (2020). Bovine Colostrum in the Treatment of Acute Diarrhea in Children: A Double-Blinded Randomized Controlled Trial. J. Trop. Pediatr. 66, 46–55. doi: 10.1093/tropej/fmz029
Bedford, A., Chen, T., Huynh, E., Zhu, C., Medeiros, S., Wey, D., et al. (2015). Epidermal growth factor containing culture supernatant enhances intestine development of early-weaned pigs in vivo: Potential mechanisms involved. J. Biotechnol. 196–197, 9–19. doi: 10.1016/j.jbiotec.2015.01.007
Bellavia, M., Rappa, F., Lo Bello, M., Brecchia, G., Tomasello, G., Leone, A., et al. (2014). Lactobacillus casei and bifidobacterium lactis supplementation reduces tissue damage of intestinal mucosa and liver after 2,4,6-trinitrobenzenesulfonic acid treatment in mice. J. Biol. Regul. Homeost. Agents 28, 251–261.
Bergman, H., Buckley, B. S., Villanueva, G., Petkovic, J., Garritty, C., Lutje, V., et al. (2019). Comparison of different human papillomavirus (HPV) vaccine types and dose schedules for prevention of HPV-related disease in females and males. Cochrane Database Syst. Rev. 2019, 1–154. doi: 10.1002/14651858.CD013479
Brandal, P., Heim, S. (2015). “Tumors of the nervous system,” in Cancer Cytogenetics: Fourth Edition (Hoboken, NJ, USA: John Wiley & Sons, Inc), 515–537. doi: 10.1002/9781118795569.ch20
Bray, F., Ferlay, J., Soerjomataram, I., Siegel, R. L., Torre, L. A., Jemal, A. (2018). Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J. Clin. 68, 394–424. doi: 10.3322/caac.21492
Bullinger, L., Döhner, K., Dohner, H. (2017). Genomics of acute myeloid leukemia diagnosis and pathways. J. Clin. Oncol. 35, 934–946. doi: 10.1200/JCO.2016.71.2208
Buttar, H. S., Bagwe, S. M., Bhullar, S. K., Kaur, G. (2017). Health Benefits of Bovine Colostrum in Children and Adults. Dairy Hum. Health Dis. Across Lifespan 12, 3–20. doi: 10.1016/b978-0-12-809868-4.00001-7
Cairangzhuoma Yamamoto, M., Muranishi, H., Inagaki, M., Uchida, K., Yamashita, K., et al. (2013). Skimmed, Sterilized, and concentrated bovine late colostrum promotes both prevention and recovery from intestinal tissue damage in mice. J. Dairy Sci. 96, 1347–1355. doi: 10.3168/jds.2012-5701
Chae, A., Aitchison, A., Day, A. S., Keenan, J. I. (2017). Bovine colostrum demonstrates anti-inflammatory and antibacterial activity in in vitro models of intestinal inflammation and infection. J. Funct. Foods 28, 293–298. doi: 10.1016/j.jff.2016.11.016
Crittenden, R., Little, C., Georgiou, G., Forsyth, S., Bennett, L. (2007). Cow’s milk allergy: A complex disorder. in. Aust. J. Dairy Technol. 24, 62–71. doi: 10.1007/s00217-005-0178-8
Cutone, A., Rosa, L., Ianiro, G., Lepanto, M. S., Bonaccorsi di Patti, M. C., Valenti, P., et al. (2020). Lactoferrin’s Anti-Cancer Properties: Safety, Selectivity, and Wide Range of Action. Biomolecules 10:456. doi: 10.3390/biom10030456
de Almeida, M. F. B., Draque, C. M. (2007). Neonatal Jaundice and Breastfeeding. Neoreviews 8, e282–e288. doi: 10.1542/neo.8-7-e282
Donovan, S. M. (2016). The Role of Lactoferrin in Gastrointestinal and Immune Development and Function: A Preclinical Perspective. J. Pediatr. 173, S16–S28. doi: 10.1016/j.jpeds.2016.02.072
Elfstrand, L., Lindmark-Månsson, H., Paulsson, M., Nyberg, L., Åkesson, B. (2002). Immunoglobulins, growth factors and growth hormone in bovine colostrum and the effects of processing. Int. Dairy J. 12, 879–887. doi: 10.1016/s0958-6946(02)00089-4
Etienne, G., Guilhot, J., Rea, D., Rigal-Huguet, F., Nicolini, F., Charbonnier, A., et al. (2017). Long-term follow-up of the French Stop Imatinib (STIM1) study in patients with chronic myeloid leukemia. J. Clin. Oncol. 35, 298–305. doi: 10.1200/JCO.2016.68.2914
Farziyan, M. A., Moradian, F., Rafiei, A. R. (2016). Anticancer Effect of Bovine Lactoferrin on Human Esophagus Cancer Cell Line. Res. Mol. Med. 4, 18–23. doi: 10.7508/rmm.2016.01.003
Florén, C. H., Chinenye, S., Elfstrand, L., Hagman, C., Ihse, I. (2006). ColoPlus, a new product based on bovine colostrum, alleviates HIV-associated diarrhoea. Scand. J. Gastroenterol. 41, 682–686. doi: 10.1080/00365520500380817
Formenti, S. C., Demaria, S. (2009). Systemic effects of local radiotherapy. Lancet Oncol. 10, 718–726. doi: 10.1016/S1470-2045(09)70082-8
França-Botelho, A. (2019). Beneficial Components of Colostrum for Cancer Patients: A Mini-review Focused on Oxidative Aspects and Properties of Colostrinin. Asian Oncol. Res. J. 2 (1), 1–6.
Gensollen, T., Iyer, S. S., Kasper, D. L., Blumberg, R. S. (2016). How colonization by microbiota in early life shapes the immune system. Science 352, 539–544. doi: 10.1126/science.aad9378
Godhia, M. L., Patel, N. (2013). Colostrum - Its composition, benefits as a nutraceutical: A review. Curr. Res. Nutr. Food Sci. 1, 37–47. doi: 10.12944/CRNFSJ.1.1.04
Good, M., Sodhi, C. P., Egan, C. E., Afrazi, A., Jia, H., Yamaguchi, Y., et al. (2015). Breast milk protects against the development of necrotizing enterocolitis through inhibition of Toll-like receptor 4 in the intestinal epithelium via activation of the epidermal growth factor receptor. Mucosal Immunol. 8, 1166–1179. doi: 10.1038/mi.2015.30
Holtmann, G., Shah, A., Morrison, M. (2017). Pathophysiology of Functional Gastrointestinal Disorders: A Holistic Overview. Dig. Dis. 35(Suppl 1), 5–13. doi: 10.1159/000485409
Huppertz, H., II, Rutkowski, S., Busch, D. H., Eisebit, R., Lissner, R., Karch, H. (1999). Bovine colostrum ameliorates diarrhea in infection with diarrheagenic Escherichia coli, Shiga toxin-producing E. coli, and E. coli expressing intimin and hemolysin. J. Pediatr. Gastroenterol. Nutr. 29, 452–456. doi: 10.1097/00005176-199910000-00015
Hurley, W. L., Theil, P. K. (2011). Perspectives on immunoglobulins in colostrum and milk. Nutrients 3, 442–474. doi: 10.3390/nu3040442
Hyrslova, I., Krausova, G., Bartova, J., Kolesar, L., Curda, L. (2016). Goat and Bovine Colostrum as a Basis for New Probiotic Functional Foods and Dietary Supplements. J. Microb. Biochem. Technol. 08, 1948–5948. doi: 10.4172/1948-5948.1000262
Ilan, Y. (2016). Oral immune therapy: targeting the systemic immune system via the gut immune system for the treatment of inflammatory bowel disease. Clin. Transl. Immunol. 5, e60. doi: 10.1038/cti.2015.47
Jacqmin, S., Vleurick, L., Renaville, R., Portetelle, D. (2000). Modulation of the biological action of bovine growth hormone by passive immunization in hypophysectomised rat. Biotechnol. Agron. Société Environ. = Biotechnol. Agron. Soc Environ. [=BASE] 3, 23–24.
Jolly, A., Mascaro, M. (2016). Evaluation of Hyaluronic Acid in Cattle: Physiological Variations Related to Age, Periparturition and in Clinical Cases of Paratuberculosis. J. Vet. Sci. Technol. 7, 342–346. doi: 10.4172/2157-7579.1000342
Kaducu, F. O., Okia, S. A., Upenytho, G., Elfstrand, L., Florén, C. H. (2011). Effect of bovine colostrum-based food supplement in the treatment of HIV-associated diarrhea in Northern Uganda: A randomized controlled trial. Indian J. Gastroenterol. 30, 270–276. doi: 10.1007/s12664-011-0146-0
Khan, Z., Macdonald, C., Wicks, A. C., Holt, M. P., Floyd, D., Ghosh, S., et al. (2002). Use of the “nutriceutical”, bovine colostrum, for the treatment of distal colitis: Results from an initial study. Aliment. Pharmacol. Ther. 16, 1917–1922. doi: 10.1046/j.1365-2036.2002.01354.x
Kim, J. H., Jung, W. S., Choi, N. J., Kim, D. O., Shin, D. H., Kim, Y. J. (2009). Health-promoting effects of bovine colostrum in Type 2 diabetic patients can reduce blood glucose, cholesterol, triglyceride and ketones. J. Nutr. Biochem. 20, 298–303. doi: 10.1016/j.jnutbio.2008.04.002
Kuemmerle, N. B., Rysman, E., Lombardo, P. S., Flanagan, A. J., Lipe, B. C., Wells, W. A., et al. (2011). Lipoprotein lipase links dietary fat to solid tumor cell proliferation. Mol. Cancer Ther. 10, 427–436. doi: 10.1158/1535-7163.MCT-10-0802
Layman, D. K., Lönnerdal, B., Fernstrom, J. D. (2018). Applications for alpha-lactalbumin in human nutrition. Nutr. Rev. 76, 444–460. doi: 10.1093/nutrit/nuy004
Le Doare, K., Holder, B., Bassett, A., Pannaraj, P. S. (2018). Mother’s Milk: A Purposeful Contribution to the Development of the Infant Microbiota and Immunity. Front. Immunol. 9:361. doi: 10.3389/fimmu.2018.00361
Linehan, W. M., Spellman, P. T., Ricketts, C. J., Creighton, C. J., Fei, S. S., Davis, C., et al. (2016). Comprehensive Molecular Characterization of Papillary Renal-Cell Carcinoma. N. Engl. J. Med. 374, 135–145. doi: 10.1056/NEJMoa1505917
Maqbool, S. (1992). Jaundice in the newborn. Specialist 8, 71–83. doi: 10.5694/j.1326-5377.1957.tb60186.x
McGowan, M. M., Eisenberg, B. L., Lewis, L. D., Froehlich, H. M., Wells, W. A., Eastman, A., et al. (2013). A proof of principle clinical trial to determine whether conjugated linoleic acid modulates the lipogenic pathway in human breast cancer tissue. Breast Cancer Res. Treat. 138, 175–183. doi: 10.1007/s10549-013-2446-9
McGrath, B. A., Fox, P. F., McSweeney, P. L. H., Kelly, A. L. (2016). Composition and properties of bovine colostrum: a review. Dairy Sci. Technol. 96, 133–158. doi: 10.1007/s13594-015-0258-x
Menchetti, L., Traina, G., Tomasello, G., Casagrande-Proietti, P., Leonardi, L., Barbato, O., et al. (2016). Potential benefits of colostrum in gastrointestinal diseases. Front. Biosci. - Sch. 8, 331–351. doi: 10.2741/s467
Menchetti, L., Curone, G., Filipescu, I. E., Barbato, O., Leonardi, L., Guelfi, G., et al. (2020). The Prophylactic Use of Bovine Colostrum in a Murine Model of TNBS-Induced Colitis. Anim. (Basel) 10, 492. doi: 10.3390/ani10030492
Meurer, M., Floquet, A., Italiano, A., Auriche, M., Mancini, J., Penel, N., et al. (2017). Undifferentiated endometrial sarcomas (UES): Results of a French sarcoma group (FSG) retrospective series of 52 patients (pts). J. Clin. Oncol. 35, e17109–e17109. doi: 10.1200/jco.2017.35.15_suppl.e17109
Miller, K. D., Nogueira, L., Mariotto, A. B., Rowland, J. H., Yabroff, K. R., Alfano, C. M., et al. (2019). Cancer treatment and survivorship statistics 2019. CA. Cancer J. Clin. 69, 363–385. doi: 10.3322/caac.21565
Miolo, G., Basile, D., Carretta, A., Santeufemia, D. A., Steffan, A., Corona, G. (2019). The metabolomic scent of cancer disease progression in soft tissue sarcoma: A case report. Int. J. Biol. Markers 34, 205–209. doi: 10.1177/1724600818817316
Mizrahi, M., Shabat, Y., Ya’acov, A.B., Lalazar, G., Adar, T., Wong, V., et al. (2012). Alleviation of insulin resistance and liver damage by oral administration of Imm124-E is mediated by increased Tregs and associated with increased serum GLP-1 and adiponectin: Results of a phase I/II clinical trial in NASH. J. Inflamm. Res. 5, 141–150. doi: 10.2147/JIR.S35227
Mohammadzadeh, M., Faramarzi, E., Mahdavi, R., Nasirimotlagh, B., Asghari Jafarabadi, M. (2013). Effect of conjugated linoleic acid supplementation on inflammatory factors and matrix metalloproteinase enzymes in rectal cancer patients undergoing chemoradiotherapy. Integr. Cancer Ther. 12, 496–502. doi: 10.1177/1534735413485417
Murata, M., Satoh, T., Wakabayashi, H., Yamauchi, K., Abe, F., Nomura, Y. (2014). Oral administration of bovine lactoferrin attenuates ultraviolet B-induced skin photodamage in hairless mice. J. Dairy Sci. 97, 651–658. doi: 10.3168/jds.2013-7153
Niezgoda, N., Gliszczyńska, A., Kempińska, K., Wietrzyk, J., Wawrzeńczyk, C. (2017). Synthesis and evaluation of cytotoxic activity of conjugated linoleic acid derivatives (esters, alcohols, and their acetates) toward cancer cell lines. Eur. J. Lipid Sci. Technol. 119:1600470. doi: 10.1002/ejlt.201600470
Osada, S. I., Yoshida, R., Kikuchi, I., Tsuruta, D., Ansai, S. I., Hashimoto, T., et al. (2014). Successful Treatment of Intravenous Immunoglobulins in a Patient with Intractable Epidermolysis Bullosa Acquisita with Autoantibodies to Type VII Collagen and Laminin Alpha-3. J. Clin. Exp. Dermatol. Res. 4, 1–3. doi: 10.4172/2155-9554.1000200
Pammi, M., Abrams, S. A. (2015). Oral lactoferrin for the prevention of sepsis and necrotizing enterocolitis in preterm infants. Cochrane Database Syst. Rev. 2, CD007137. doi: 10.1002/14651858.CD007137.pub4
Pieper, R., Scharek-Tedin, L., Zetzsche, A., Röhe, I., Kröger, S., Vahjen, W., et al. (2016). Bovine milk–based formula leads to early maturation-like morphological, immunological, and functional changes in the jejunum of neonatal piglets. J. Anim. Sci. 94, 989–999. doi: 10.2527/jas.2015-9942
Playford, R. J., Floyd, D. N., Macdonald, C. E., Calnan, D. P., Adenekan, R. O., Johnson, W., et al. (1999). Bovine colostrum is a health food supplement which prevents NSAID induced gut damage. Gut 44, 653–658. doi: 10.1136/gut.44.5.653
Playford, R. J., Macdonald, C. E., Calnan, D. P., Floyd, D. N., Podas, T., Johnson, W., et al. (2001). Co-administration of the health food supplement, bovine colostrum, reduces the acute non-steroidal anti-inflammatory drug-induced increase in intestinal permeability. Clin. Sci. 100, 627–633. doi: 10.1042/CS20010015
Pluske, J. R. (2016). Invited review: Aspects of gastrointestinal tract growth and maturation in the pre- and postweaning period of pigs. J. Anim. Sci. 94, 399–411. doi: 10.2527/jas.2015-9767
Rajyaguru, D. J., Borgert, A. J., Smith, A. L., Thomes, R. M., Conway, P. D., Halfdanarson, T. R., et al. (2018). Radiofrequency Ablation Versus Stereotactic Body Radiotherapy for Localized Hepatocellular Carcinoma in Nonsurgically Managed Patients: Analysis of the National Cancer Database. J. Clin. Oncol. 36, 600–608. doi: 10.1200/JCO.2017.75.3228
Rathe, M., De Pietri, S., Wehner, P. S., Frandsen, T. L., Grell, K., Schmiegelow, K., et al. (2019). Bovine Colostrum Against Chemotherapy-Induced Gastrointestinal Toxicity in Children With Acute Lymphoblastic Leukemia: A Randomized, Double-Blind, Placebo-Controlled Trial. J. Parenter. Enter. Nutr. 44, 337–347. doi: 10.1002/jpen.1528
Rawal, P., Gupta, V., Thapa, B. R. (2008). Role of colostrum in gastrointestinal infections. Indian J. Pediatr. 75, 917–921. doi: 10.1007/s12098-008-0192-5
Rokka, S., Myllykangas, S., Joutsjoki, V. (2008). Effect of specific colostral antibodies and selected lactobacilli on the adhesion of Helicobacter pylori on AGS cells and the Helicobacter-induced IL-8 production. Scand. J. Immunol. 68, 280–286. doi: 10.1111/j.1365-3083.2008.02138.x
Rosenberg, J. E., Petrylak, D. P., Van Der Heijden, M. S., Necchi, A., O’Donnell, P. H., Loriot, Y., et al. (2016). PD-L1 expression, Cancer Genome Atlas (TCGA) subtype, and mutational load as independent predictors of response to atezolizumab (atezo) in metastatic urothelial carcinoma (mUC; IMvigor210). IJCO 34, 104–104. doi: 10.1200/JCO.2016.34.15_suppl.104
Rugge, M., Fassan, M., Graham, D. Y. (2015). “Epidemiology of gastric cancer,” in Gastric Cancer: Principles and Practice. (Cham, Switzerland: Springer International Publishing) 23–34. doi: 10.1007/978-3-319-15826-6_2
Seebacher, N. A., Stacy, A. E., Porter, G. M., Merlot, A. M. (2019). Clinical development of targeted and immune based anti-cancer therapies. J. Exp. Clin. Cancer Res. 38, 156. doi: 10.1186/s13046-019-1094-2
Sequeira, E., Kaur, G., Buttar, H. S. (2014). Celiac disease: Role of genetics and immunity and update on novel strategies for treatment. Biomed. Rev. 25, 45–58. doi: 10.14748/bmr.v25.1047
Shah, N. P. (2000). Effects of milk-derived bioactives: an overview. Br. J. Nutr. 84(Suppl 1), S3–10. doi: 10.1017/s000711450000218x
Shahzad, M. M. K., Felder, M., Ludwig, K., Van Galder, H. R., Anderson, M. L., Kim, J., et al. (2018). Trans10,cis12 conjugated linoleic acid inhibits proliferation and migration of ovarian cancer cells by inducing ER stress, autophagy, and modulation of Src. PLoS One 13, e0189524. doi: 10.1371/journal.pone.0189524
Sharma, A., Shandilya, U. K., Sodhi, M., Mohanty, A. K., Jain, P., Mukesh, M. (2019). Evaluation of Milk Colostrum Derived Lactoferrin of Sahiwal () and Karan Fries (Cross-Bred) Cows for Its Anti-Cancerous Potential. Int. J. Mol. Sci. 20, 6318. doi: 10.3390/ijms20246318
Shen, R. L., Thymann, T., Østergaard, M. V., Støy, A. C. F., Krych, Ł., Nielsen, D. S., et al. (2015). Early gradual feeding with bovine colostrum improves gut function and NEC resistance relative to infant formula in preterm pigs. Am. J. Physiol. - Gastrointest. Liver Physiol. 309, G310–G323. doi: 10.1152/ajpgi.00163.2015
Siegel, R. L., Miller, K. D., Jemal, A. (2016). Cancer statistics 2016. CA. Cancer J. Clin. 66, 7–30. doi: 10.3322/caac.21332
Stefani, C., Liverani, C. A., Bianco, V., Penna, C., Guarnieri, T., Comparetto, C., et al. (2014). Spontaneous regression of low-grade cervical intraepithelial lesions is positively improved by topical bovine colostrum preparations (GINEDIE®). A multicentre, observational, italian pilot study. Eur. Rev. Med. Pharmacol. Sci. 18, 728–733.
Stelwagen, K., Carpenter, E., Haigh, B., Hodgkinson, A., Wheeler, T. T. (2009). Immune components of bovine colostrum and milk. J. Anim. Sci. 87, 3–9. doi: 10.2527/jas.2008-1377
Støy, A. C. F., Heegaard, P. M. H., Thymann, T., Bjerre, M., Skovgaard, K., Boye, M., et al. (2014). Bovine colostrum improves intestinal function following formula-induced gut inflammation in preterm pigs. Clin. Nutr. 33, 322–329. doi: 10.1016/j.clnu.2013.05.013
Sugihara, Y., Zuo, X., Takata, T., Jin, S., Miyauti, M., Isikado, A., et al. (2017). Inhibition of DMH-DSS-induced colorectal cancer by liposomal bovine lactoferrin in rats. Oncol. Lett. 14, 5688–5694. doi: 10.3892/ol.2017.6976
Takayama, Y., Kitsunai, K., Mizumachi, K. (2001). Factors in bovine colostrum that enhance the migration of human fibroblasts in type I collagen gels. Biosci. Biotechnol. Biochem. 65, 2776–2779. doi: 10.1271/bbb.65.2776
Taylor, C. W., Kirby, A. M. (2015). Cardiac Side-effects From Breast Cancer Radiotherapy. Clin. Oncol. 27, 621–629. doi: 10.1016/j.clon.2015.06.007
Teixeira, F. J., Santos, H. O., Howell, S. L., Pimentel, G. D. (2019). Whey protein in cancer therapy: A narrative review. Pharmacol. Res. 144, 245–256. doi: 10.1016/j.phrs.2019.04.019
Tran, C. D., Kritas, S., Campbell, M. A. F., Huynh, H. Q., Lee, S.-S., Butler, R. N. (2010). Novel combination therapy for the eradication of Helicobacter pylori infection in a mouse model. Scand. J. Gastroenterol. 45, 1424–1430. doi: 10.3109/00365521.2010.506245
Tricoli, J. V., Blair, D. G., Anders, C. K., Bleyer, W. A., Boardman, L. A., Khan, J., et al. (2016). Biologic and clinical characteristics of adolescent and young adult cancers: Acute lymphoblastic leukemia, colorectal cancer, breast cancer, melanoma, and sarcoma. Cancer 122, 1017–1028. doi: 10.1002/cncr.29871
Tsuda, H., Fukamachi, K., Xu, J., Sekine, K., Ohkubo, S., Takasuka, N., et al. (2006). Prevention of carcinogenesis and cancer metastasis by bovine lactoferrin. Proc. Jpn. Acad. Ser. B Phys. Biol. Sci. 82, 208–215. doi: 10.2183/pjab.82.208
Tung, Y. T., Chen, H. L., Yen, C. C., Lee, P. Y., Tsai, H. C., Lin, M. F., et al. (2013). Bovine lactoferrin inhibits lung cancer growth through suppression of both inflammation and expression of vascular endothelial growth factor. J. Dairy Sci. 96, 2095–2106. doi: 10.3168/jds.2012-6153
Ulfman, L. H., Leusen, J. H. W., Savelkoul, H. F. J., Warner, J. O., van Neerven, R. J. J. (2018). Effects of Bovine Immunoglobulins on Immune Function, Allergy, and Infection. Front. Nutr. 5:52. doi: 10.3389/fnut.2018.00052
Vitetta, E. S., Krolick, K. A., Miyama-Inaba, M., Cushley, W., Uhr, J. W. (2019). “Immunotoxins: A New Approach to Cancer Therapy”, in Biotechnology and Biological Frontiers, Ed. Abelson, P. H. (Routledge), 73–85. doi: 10.4324/9780429050329-7
Waaga-Gasser, A. M., Gasser, M., Stock, M., Grimm, M., Sprotte, G. (2009). Oral immunoglobulin induces mononuclear cell apoptosis in patients suffering from idiopathic chronic pain syndrome: Results from a pilot study. Int. J. Clin. Pharmacol. Ther. 47, 421–433. doi: 10.5414/CPP47421
Wu Xiaoyun, S. P. S., Xiong Lin, D.x. (2015). The Influence of Heat Treatment in Liquid Whey at Various pH on Immunoglobulin G and Lactoferrin from Yak and Cows’ Colostrum/Milk. J. Food Process. Technol. 6, 1–9. doi: 10.4172/2157-7110.1000503
Xu, M. L., Kim, H. J., Wi, G. R., Kim, H. J. (2015). The effect of dietary bovine colostrum on respiratory syncytial virus infection and immune responses following the infection in the mouse. J. Microbiol. 53, 661–666. doi: 10.1007/s12275-015-5353-4
Yadav, R., Angolkar, T., Kaur, G., Buttar, H. S. (2016). Antibacterial and Antiinflammatory Properties of Bovine Colostrum. Recent Pat. Inflamm. Allergy Drug Discov. 10, 49–53. doi: 10.2174/1872214810666160219163118
Ya’acov, A.B., Lichtenstein, Y., Zolotarov, L., Ilan, Y. (2015). The gut microbiome as a target for regulatory T cell-based immunotherapy: Induction of regulatory lymphocytes by oral administration of anti-LPS enriched colostrum alleviates immune mediated colitis. BMC Gastroenterol. 15, 45–93. doi: 10.1186/s12876-015-0388-x
Keywords: inflammatory bowel disease (IBD), anticancer therapy, antimicrobial activity, cervical intraepithelial neoplasia, proline-rich polypeptide, immunoglobulins, conjugated linoleic acid
Citation: Bagwe-Parab S, Yadav P, Kaur G, Tuli HS and Buttar HS (2020) Therapeutic Applications of Human and Bovine Colostrum in the Treatment of Gastrointestinal Diseases and Distinctive Cancer Types: The Current Evidence. Front. Pharmacol. 11:01100. doi: 10.3389/fphar.2020.01100
Received: 27 January 2020; Accepted: 06 July 2020;
Published: 11 September 2020.
Edited by:
Lokesh Bhatt, Dr. Bhanuben Nanavati College of Pharmacy, IndiaReviewed by:
Mizuho Inagaki, Gifu University, JapanSaartjie Roux, Nelson Mandela University, South Africa
Copyright © 2020 Bagwe-Parab, Yadav, Kaur, Tuli and Buttar. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Ginpreet Kaur, Ginpreet.Kaur@nmims.edu; Hardeep Singh Tuli, hardeep.biotech@gmail.com