Skip to main content
Download PDF
  • Research article
  • Open access
  • Published:

Role of HPV 16 variants among cervical carcinoma samples from Northeastern Brazil

BMC Women's Health volume 20, Article number: 162 (2020) Cite this article

Abstract

Background

Cervical cancer is the fourth most common type of cancer affecting women globally. In Brazil, it is the third most frequent type of cancer in women and HPV is present in approximately 90% of cases. Evidence suggests that variants of HPV 16 can interfere biologically and etiologically during the development of cervical cancer.

Methods

Cervix tumor fragments were collected, their DNA was extracted, and nested PCR was used to detect HPV. Positive samples were sequenced to determine the viral genotype. To characterize the HPV 16 strains, positive samples PCR was used to amplify the LCR and E6 regions of the HPV 16 virus.

Results

Data from 120 patients with cervical cancer were analyzed. Most women were between 41 and 54 years of age, had schooling until primary school, a family income between 1 and 2 times the minimum wage and were married/in a consensual union. There was no statistically significant association between HPV or socio-demographic variables and risk factors for cervical cancer (P <  0.05). HPV was present in 88 women (73%). The most prevalent types were HPV 16 (53.4%), HPV 18 (13.8%), HPV 35 (6.9%) and HPV 45 (5.7%). Of the 47 HPV 16 positive cases, variant A (49%) was present in 23 samples, followed by variant D in 20 cases (43%), and variants B and C in 2 cases each (4%). The most prevalent histological type of HPV 16 tumors was squamous cell carcinoma, followed by adenocarcinoma. There was a statistically significant association between HPV 16 variants and the tumors’ histological types (P <  0.001).

Conclusions

Knowledge of HPV 16 variants will provide data on their influence on the pathological and oncogenic aspects of cervical lesions.

Peer Review reports

Background

Cervical cancer is the fourth most common cancer type affecting women worldwide, with more than 265,000 estimated deaths annually and more than 80% of cases occurring in developing countries [1, 2]. According to INCA, cervical cancer is the third most common cancer type in the Brazilian female population. They estimate that there will be 16,370 new cervical cancer cases for the biennium from 2018 to 2019 [3].

It is estimated that in the state of Maranhão there will be around 1090 new cervical cancer cases for 2018, with240 of them the capital, São Luís, with a gross rate of incidence of 30.55 cases per 100,000 inhabitants [3].

Human Papillomavirus (HPV) is the main etiological factor for cervical cancer and is associated with the development of diseases ranging from benign warts to invasive cancer [4]. Although approximately 80% of women acquire HPV infection by the age of 50, less than 1% of persistent infections progress to invasive cervical cancer [5].

The reason why only some uterine cervical lesions associated with high-risk genotypes progress to invasive cancer remains unknown. Evidence suggests that variants of the same HPV type can interact biologically and etiologically during cancer development [6, 7].

The HPV16 is the most carcinogenic HPV type followed by HPV18 and most infections are asymptomatic [8]. A few studies have been conducted in Brazil on HPV 16 variants. This type of study has never been conducted in Maranhão. Interest in this topic has been growing in recent years, with variation in carcinoma prognosis at different stages of the disease depending on the viral variant found attracting special interest. Even in research carried out other places in the world, many of these questions remain unclear and many of the findings are contradictory, making it necessary to develop new and continuous approaches to this topic.

Despite of the relationship between different HPV type and the development of cancer being well established, evidence suggests that genetic variations between the same viral type may influence infection potential, viral persistence, the development of precursor lesions and the progression to invasive cancer [9,10,11,12]. Due to the high prevalence of HPV 16 in cases of cervical cancer, the association between HPV 16 and cancer has been studied at the level of intratype variants, and several lines of study have attributed a higher risk of invasive cervical cancer to some HPV 16 strains.

Studies on HPV variants have been developed with the objective of understanding their association with pathological and oncogenic aspects of cervical lesions. Factors influencing HPV infection in cervical cancer are not completely clear, but it is believed that HPV 16 variants playa fundamental role in cervical carcinogenesis and are currently recognized as an important marker for research on viral transmission, persistence and carcinogenicity [5]. Variation in these aspects may contribute to disparities in cervical cancer incidence.

Regarding these aspects, the aim of this study was to evaluate the prevalence of HPV 16 variants in cervical carcinoma samples from Northeastern, Brazil. This is the first evaluation of genetic diversity of HPV 16 in the State of Maranhão, Brazil.

Methods

Type of Study

This is descriptive, prospective, and transversal study.

Period and location of study

The study was conducted from January 2016 to December 2017, at the High Complexity Care Unit (UNACON) of the Cancer State Hospital of Maranhão and in the High Complexity Care Center in Oncology (CACON) of the Aldenora Bello Cancer Hospital. This work was approved by the Research Ethics Committee of the Federal University of Maranhão (CEP-UFMA), under Consolidated Opinion N° 1.289.419/2015.

Population and sample

The study population was composed of 120 women with a diagnosis of cervical cancer, who were treated at the previously mentioned hospitals.

Inclusion criteria

Women older than 18 years diagnosed with cervical cancer who agreed to participate in the study by signing an Informed Consent Form (ICF).

Exclusion criteria

Women who presented with surgical indications as an initial treatment or who presented with small lesions, in which biopsy could interfere with staging. Women in psychiatric treatment were also excluded.

Collection instrument and data evaluation

Initially, the patients were referred for outpatient care at the Oncology Gynecology Service of the Cancer State Hospital of Maranhão and the Aldenora Bello Cancer Hospital and were invited to participate in the study by signing an Informed Consent Form (ICF). A questionnaire was supplied to collect socio-demographic, reproduction, and smoking data.

Further, women were submitted to gynecological examination. A cervical biopsy was done and cervical tumor fragments were then placed in microtubes containing 1 mL of RNA Later solution (Life Technologies) at 4 °C and were transported in thermal boxes to the Multiuser Laboratory in the Biobank of Tumors and DNA of Maranhão of the Federal University of Maranhão, University Hospital of the Federal University of Maranhão (HUUFMA). After 24 h, the samples were removed from the RNA Later solution and stored in a freezer at − 80 °C until use.

Experimental procedures

Detection of HPV DNA

The extraction of the genomic DNA from the samples was performed using the QIAamp DNA FFPE Tissue Purification Kit (QIAGEN®) according to manufacturer protocols.

The Nested PCR reactions were performed by using primers PGMY09 and PGMY11 for the first round, and primers GP + 5 and GP + 6 for the second round [12] (Table 1).

Table 1 Primer sequences used for PCR reaction to identify HPV DNA
Full size table

Sanger sequencing method

HPV genotypes were determined by Sanger sequencing method using a1000 MegaBACE sequencer (GE Healthcare, UK) at the Molecular Biology Laboratory of the State University of Maranhão located in the Center of Higher Studies of Caxias (CESC-UEMA).

Sequencing was performed with an ET Dye Terminator Cycle Sequencing Kit (GE Healthcare, UK), according to the manufacturer’s protocol.

The Chromas program was used to obtain electropherograms of the HPV DNA sequences present in the samples. To identify the HPV type the nucleotide sequences were compared to the Genbank Nucleotide Sequence Database using the BLAST program (NCBI).

Identification of HPV 16 variants

After determination of the HPV 16 strains, the LCR regions and E6 virus gene of the positive samples were amplified with specific primers. The reaction mixture consisted of a final volume of 25 μL, with 1X PCR Buffer, 2.5 mM of MgCl2, 0.25 μM of each dNTP, 100 pmol/L of each primer, 50–100 ng of DNA, and 2.5 U of Platinum Taq Polymerase. The PCR reaction consisted of denaturation at 95 °C for 10 min, followed by 40 cycles of 95 °C for 1 min; annealing temperature for 1 min and 72 °C for 1 min, followed by a final extension step for 15 min.

The PCR product was subsequently purified and sequenced according to the above protocol. The consensus sequences were merged using the Geneious software (Biomatters Ltd.) and all the sequences generated were aligned with HPV 16 specific strains, using the reference sequences proposed by Burk et al. [13], using the MEGA Software (version 6.0, www.megasoftware.net). BLAST online (Available at: http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/blast/Blast.cgi) was then used to identify the HPV types.

Phylogenic analysis

The phylogenetic tree of the HPV 16 strains was constructed from the 1300 bp sequences from the E6 and LCR regions using the “neighbor joining” method with p-distance (obtained with pairwise deletion) using the program Mega 4.1. The references proposed by Burk et al. (2013) [13] were included. The analysis of the HPV 16 variants was performed at the National Cancer Institute (INCA) under the supervision of Dr. Miguel Ângelo Martins Moreira.

We have provided GenBank accession numbers for nucleotide sequences: MT568878 to MT568924.

International Federation of Obstetrics and Gynecology (FIGO) system for cervical cancer

The cervical carcinoma samples were classified according to FIGO staging system [14].

Statistical analyses

Descriptive statistical analysis was performed using the Stata program (version 14.0). The x2 (Chi-square) test was used to verify the association between HPV and sociodemographic and clinical variables, and P values ≤0.05 were considered statistically significant. The values corresponding to don’t know/did not respond were excluded from the association analysis.

Results

Sociodemographic and clinical data

Among the women diagnosed with cervical cancer, HPV was present in 88 (73.3%). The majority of these women were in the age group 40 to 49 years of age (28.3%), and self-declared with mixed-race (70%), had schooling up to elementary school (42.5%), had a family income between 1 and 2 times the minimum wage (55%) and were married or in a consensual union (51.7%). There was no statistically significant association between the sociodemographic variables and the presence of HPV (p < 0.05) (Table 2).

Table 2 Association between sociodemographic factors and the presence of HPV
Full size table

Of the risk factors associated with cervical cancer, for most women first sexual intercourse occurred between 10 and 19 years of age (72.5%), a first pregnancy between 16 and 21 (34.2%) and 1 to 3 children (30.8%) were most common. Having only one sexual partner during their lifetime (31.7%) was most common followed by more than 3 partners (30%). Most women reported never having used contraceptive methods (58.3%) (Table 3).

Table 3 Association between cervical cancer risk factors, reproductive history and presence of HPV
Full size table

Most women (70%) reported having undergone examination before their diagnosis with cervical cancer and most (36.7%) said they received preventive exam annually. Most women reported no tobacco use (57.5%) (Table 4).

Table 4 Association between preventive examination, smoking and the presence of HPV
Full size table

Identification of HPV type

HPV was present in 88 women (73.3%). The most prevalent type was HPV 16, which accounts for 53.4%(47/88) and combined with HPV 18 accounted for 67.2% of cases. Most of the samples had HPV types considered high risk, while less than 3.4% had HPV types considered to have low oncogenic risk (Fig. 1).

Fig. 1
figure 1

Prevalence of HPV subtypes in cervical carcinoma samples from São Luis, Maranhão, Brazil

Full size image

Histological types of analyzed tumors

The most prevalent types of tumor histological types were squamous cell carcinoma with a total of 95 cases (79.1%) and 11 (9.1%) cases of adenocarcinomas. Of the 120 women in this study, 45 (37.5%) had stage IIIB tumors, in cases where HPV 16 was present, stage III was predominant with 23 samples, according to FIGO classification.

HPV 16 variants

Of the 47 samples identified as HPV 16, 23 samples were variant A (49%), 20 (43%) were variant D, while variants B and C were present in two samples each (4%).

The mean age for women with variant A of HPV 16 was 50.6 years, 58.5 years for variant B, 58.5 years for variant C and 50 years for those with variant D (Table 5). The most prevalent histological type in tumors with HPV 16 was squamous cell carcinoma (SCC) in 38 samples, followed by adenocarcinoma in 4 samples (11%) (Table 5).

Table 5 Relationship between age, histological types and HPV 16 variants
Full size table

There was a statistically significant association between histological type and HPV variant (p < 0,001), regarding squamous cell carcinoma and HPV 16 variant “A” and “D” (Table 5).

Staging also changed depending on the HPV 16 variant. Among patients with variant A, stage III (9 patients) was predominant followed by stage II (8 cases). For those with variant D, clinical stage III (10 cases) was predominant, followed by stage II (4 cases) (Table 6).

Table 6 Analysis between clinical stage and HPV 16 variants
Full size table

Treatment response also depended on the HPV 16 variant. For example, 12 cases with variant A showed complete remission, compared to only 7 cases with variant D. Likewise, there were 2 deaths with variant A, and 3 who had variant D. In 12 cases it was not possible to evaluate disease status at the end of the first treatment (Table 7).

Table 7 Analysis between treatment response and HPV 16 variants
Full size table

HPV sublineages

A reference sequence described by Burk et al. [13] was used to construct the phylogenetic tree.

Among HPV 16 cervical samples classified as belonging to variant A, 21 belonged to sublineage A1, 1 belonged to sublineage A2 and 1 belonged to sublineage A4. Of the samples belonging to variant B, 1 belonged to sublineage B1 and 1 belonged to sublineage B2 (Fig. 2).

Fig. 2
figure 2

Phylogenetic tree of HPV 16 with lineages. The tree was constructed using Neighbor-Joining with pairwise deletion. The numbers at each node are bootstrap values (with 1000 replicates)

Full size image

Of the HPV 16 cervical samples belonging to variant D, 1 belonged to sublineage D1, 1 belonged to sublineage D2 and 18 belonged to sublineage D3. Variant C, with 2 cases, does not have any sublineages (Fig. 2).

Discussion

Our research evidenced that the majority of women were in the age group 40 to 49 years of age and self-declared with mixed-race, had schooling up to elementary school, had a family income between 1 and 2 times the minimum wage and were married or in a consensual union. There was no statistically significant association between the sociodemographic variables and the presence of HPV.

Cervical cancer is associated with low socioeconomic indices, presenting a higher prevalence in regions with high poverty, high illiteracy rates and precarious hygiene habits [15, 16].

A study by Wang et al. (2015) [17] reported that women who received Pap smear test tended to have higher education levels, corroborating the results of other studies, and that this may be associated with a lack of information and delays in searching for treatment. In a study conducted by Manga et al. (2015) [18] on 209 women who sought care for cervical cancer screening, the mean age was 39.6 years old, and only 15% of the women were not literate, 88% were married and 48% had a paid activity.

The virus was highly prevalent (88/120–73%) in the tumor samples examined. The prevalence of HPV in invasive cervical cancer samples can range from 70 to 100%, which may be associated with different techniques used to detect the virus [19,20,21].

HPV 16 is the most prevalent in cervical cancer worldwide, followed by HPV 18. However, the frequency of HPV types may vary according to the geographic region of the population under analysis. Other studies point out that types 16, 18, 31, and 45as the four most prevalent HPV types in South and Central America [13, 21].

Studies have sought to evaluate the role of intratype variants of HPV16 and HPV18 in the persistence of viral infection, the risk of cervical intraepithelial neoplasia development, and the development of invasive cervical cancer [11, 13]. For both HPV 16 and HPV 18, the distribution of variants worldwide is influenced by geographic and ethnic factors.

In the present study in São Luís do Maranhão, the most prevalent strain in the population studied was variant A for HPV 16, according to the literature. In a case-control study conducted by Hang et al. (2016) [5], we attempted to evaluate the association between HPV 16 variants and the risk of cervical cancer in 298 women with HPV 16 in China and found that variant A was predominant.

In the study conducted by Volpini et al., (2017) [22] in Brazil on 24 women positive for HPV 16, with HIV diagnosis, but anormal Pap smear, variant A accounted for 70.8% of cases (17/24), followed by the C and D variants, which together totaled 29.2% of the samples (7/24).

In a study conducted in Brazil by Vidal et al. (2016) [12] on a cohort of 594 women with invasive cervical cancer, 334 women had HPV 16. Of these, 217 (65%) belonged to variant A, 97 (29%) belonged to variant D. Variants B and C had 10 cases (3%) each.

A study by Villa et al. (2000) [23], also in Brazil, examined the geographic differences in intratype variations of HPV 16 and their associations with the development of cervical cancer precursor lesions. Variant A (54%) was the most frequent, followed by variant D in 22% of the cases. It also emphasizes the strong association between persistence and the presence of the non-European variants B, C and D when compared to the European prototype A.

The most prevalent histological type in tumors with HPV 16 was squamous cell carcinoma (SCC) in 38 samples. There was a statistically significant association between histological type and HPV variant (p < 0,001).

Staging also changed depending on the HPV 16 variant. Among patients with variant A, stage III (9 patients) was predominant.

Studies also indicate a variation in the distribution of HPV types among histological types. HPV 16 has been associated with squamous cell carcinoma and HPV 18 has a higher prevalence in adenocarcinoma than HPV 16. However, few studies have attempted to identify associations between HPV 16 variants and the histologic type of cervical tumors [24, 25].

In the study by Hang et al. (2016) [5], it was observed among the cases of women with cervical cancer infected with HPV 16, 289 (97%) had a pattern of squamous cell carcinoma, followed by adenocarcinoma (2.3%) and adenosquamous carcinoma (0.7%).

Treatment response also depended on the HPV 16 variant. For example, 12 cases with variant A showed complete remission, compared to only 7 cases with variant D. Likewise, there were 2 deaths with variant A, and 3 who had variant D. In 12 cases it was not possible to evaluate disease status at the end of the first treatment.

Tan et al (2019) reported that European prototype E-T350 was the most prevalent (82.76%) followed by Asian (As) variant. In patients with suspected cervical lesions the most prevalent variant was As variant (54.9%) by increasing significance with severity of cervical diseases [26].

In another study conducted by Ortiz-Ortiz et al (2015), the variants more frequently found in women with cervical carcinoma were E-G350, AA-a, AA-c, E-C188/G350 and E-A176/G350. All of them are associated with the development of cervical carcinoma, however, AA-a showed the highest association [27].

Few studies have been conducted to evaluate the effect of HPV 16 variants on the response to oncologic treatment. After analyzing 155 cases of HPV16 positive cervical cancer (132 cases of variants E × 23 cases of NE variants) Zuna et al (2011) [28] came to the conclusion that the non-European variants showed less aggressive behavior in relation to mortality than the European variants. It should be pointed out that the data should be evaluated with caution due to the small number of cases of NE variants in the study.

In our study we found a greater number of NE variants (B, C, and D). Of the 47 cases we found 23 with variant A (E) and 24 with variants B, C, and D. The mortality of patients with the NE variants was 13% (3/24), while it was 9% (2/23) in those with variant A (E). The number of cases of complete remission was also lower with the NE variants (33% × 52%). These findings can be explained by the large number of cases of variant D in our study (20 cases). A study by Burk et al (2013) [13], showed the specific aggressiveness of this variant.

We observed the predominance of sublineage A1 (21 cases), followed by sublineage D3 (18 cases). In the study by Hang et al (2016) [5], the A4 sublineage was associated with a significantly higher risk of cervical cancer than the A1-A3 sublineages (OR = 1.72, 95% CI).

In a study by Alfaro et al., (2016) [29] of 462 women with cervical cancer, HPV 16 was identified in 50.9% of the cases. Of these, the A1\2 (31.4%) sublineage was predominant, followed by the D2 (10.4%) and D3 (9.1%) sublineages. However, AA variants accounted for 38.7% of the HPV 16 positive cases.

A study by Nicolas-Parraga et al. (2017) [30], sought to explore the prevalence of HPV 16 variants in patients with cervical cancer from Europe, South-Central America, Asia and Africa. One hundred eighteen cases of squamous cell carcinoma, 120 of adenocarcinoma, and 53 of adenosquamous carcinoma were observed. Also, the highest prevalence of HPV 16 was observed in patients with squamous cell carcinoma. When examining HPV 16 variants, the A1–3 sublineages were predominant in squamous cell carcinomas (76.9 to 97% for different geographic regions) and there was a large variation for variant D depending on the geographic region in adenocarcinoma (28.6 to 63.3% for different geographic regions), and adenosquamous carcinoma (12.5 to 61.5% for different geographic regions).

The data also showed an increase in the prevalence of A1–3 in Europe (67.9 to 97% for all histological types), variant D in South-Central America (61.5 to 63%, for adenocarcinoma and adenosquamous carcinoma), A4 in Asia (from 11.5 to 27.6% for all types) and variants B and C for Africa (from 28 to 66.7% and from 12.3 to 37.5% for ECC and ADC) [30].

Conclusions

The most prevalent HPV in cervical carcinoma samples in São Luís was HPV 16. This study evidenced for the first time the prevalence of HPV variants ant the most prevalent was variant A. There was a statistically significant association between histological type and HPV variant.

Further studies are needed to understand the role of HPV variants in the origin and progression of cervical cancer, as well as the relationship between HPV 16 and its variants with the development of precursor lesions. The data presented here may help the development of future epidemiological studies on HPV 16 variants, as well as in the creation of strategies to combat the types that remain circulating, and which were not included in the currently available vaccines against HPV.

Availability of data and materials

All data is included in the manuscript file. The data bank is available with the authors.

Abbreviations

ADC:

Adenocarcinoma

BLAST:

Basic Local Alignment Search Tool

CACON:

High Complexity Care Center in Oncology

CEP-UFMA:

Research Ethics Committee of the Federal University of Maranhão

CESC-UEMA:

Center of Advanced Studies of Caxias of State University of Maranhão

DNA:

Deoxyribonucleic acid

FAPEMA:

Support Foundation for research and scientific and technological development of the State of Maranhão

FIGO:

International Federation of Gynecology and Obstetrics

HPV:

Human papillomavirus

ICF:

Informed Consent Form

INCA:

National Institute of Cancer

HUUFMA:

University Hospital From Federal University of Maranhão

LCR:

Long control region

MEGA:

Molecular Evolutionary Genetics Analysis

PCR:

Polymerase chain reaction

PDC:

Poorly differentiated carcinoma

RNA:

Ribonucleic acid

SCC:

Squamous cell carcinoma

UMT:

Undifferentiated malignant tumor

References

  1. Bahls L, Yamakawa R, Zanão K, Alfieri D, Flauzino T, Delongui F, et al. Human leukocyte antigen class I and class II polymorphisms and serum cytokine profiles in cervical Cancer. Int J Mol Sci. 2017;18(9):1478.

  2. Barroeta JE, Adhikari-Guragain D, Grotkowski CE. Cervical cancer screening in the era of HPV vaccination: a review of shifting paradigms in cytopathology. Diagn Cytopathol. 2017 Oct;45(10):903–14.

    Article  Google Scholar 

  3. Instituto Nacional de Câncer. Estimativa 2018: incidência de câncer no Brasil / Instituto Nacional de Câncer José Alencar Gomes da Silva. Coordenação de Prevenção e Vigilância. – Rio de Janeiro: INCA, 128p. 2017.

  4. Doorbar J, Egawa N, Griffin H, Kranjec C, Murakami I. Human papillomavirus molecular biology and disease association. Rev Med Virol. 2015;25(Suppl 1):2–23.

    Article  CAS  Google Scholar 

  5. Hang D, Yin Y, Han J, Jiang J, Ma H, Xie S, et al. Analysis of human papillomavirus 16 variants and risk for cervical cancer in Chinese population. Virology. 2016;488:156–61.

    Article  CAS  Google Scholar 

  6. Bernard HU, Calleja-Macias IE, Dunn ST. Genome variation of human papillomavirus types: phylogenetic and medical implications. Int J Cancer. 2006;118(5):1071–6.

    Article  CAS  Google Scholar 

  7. Xi LF, Koutsky LA, Hildesheim A, Galloway DA, Wheeler CM, Winer RL, et al. Risk for high-grade cervical intraepithelial neoplasia associated with variants of human papillomavirus types 16 and 18. Cancer Epidemiol Biomark Prev. 2007;16(1):4–10.

    Article  CAS  Google Scholar 

  8. Chen W, Molijn A, Enqi W, Zhang X, Jenkins D, Yu X, et al. The variable clinicopathological categories and role of human papillomavirus in cervical adenocarcinoma: a hospital based nation-wide multi-center retrospective study across China. Int J Cancer. 2016;139(12):2687–97.

    Article  CAS  Google Scholar 

  9. Bernard HU. The clinical importance of the nomenclature, evolution and taxonomy of human papillomaviruses. J Clin Virol. 2005;32(Suppl 1):S1–6.

    Article  Google Scholar 

  10. Tamegão-Lopes BP, Sousa-Júnior EC, Passetti F, Ferreira CG, de Mello WA, Duarte Silvestre RV. Prevalence of human papillomavirus infection and phylogenetic analysis of HPV-16 E6 variants among infected women from northern Brazil. Infect Agent Cancer. 2014;9:25.

    Article  Google Scholar 

  11. Chen AA, Gheit T, Franceschi S, Tommasino M, Clifford GM, IARC HPV Variant Study Group. Human papillomavirus 18 genetic variation and cervical cancer risk worldwide. J Virol. 2015;89(20):10680–7.

    Article  CAS  Google Scholar 

  12. Vidal JP, Felix SP, Chaves CB, Patury P, Franco VF, de Morais EA. Genetic diversity of HPV16 and HPV18 in Brazilian patients with invasive cervical cancer. J Med Virol. 2016;88(7):1279–87.

    Article  CAS  Google Scholar 

  13. Burk RD, Harari A, Chen Z. Human papillomavirus genome variants. Virology. 2013;445(1–2):232–43.

    Article  CAS  Google Scholar 

  14. Bhatla N, Berek JS, Fredes MC, Denny LA, Grenman S, Karunaratne K, et al. Revised FIGO staging for carcinoma of the cervix uteri. Int J Gynecol Obstet. 2018;143(suppl 3):43–991.

    Google Scholar 

  15. Castellsagué X, Schneider A, Kaufmann AM, Bosch FX. HPV vaccination against cervical cancer in women above 25 years of age: key considerations and current perspectives. Gynecol Oncol. 2009;115(3 Suppl):S15–23.

    Article  CAS  Google Scholar 

  16. Pinho-França JR, Chein MBDC, Thuler LCS. Patterns of cervical cytological abnormalities according to the human development index in the northeast region of Brazil. BMC Womens Health. 2016;16:54.

    Article  Google Scholar 

  17. Wang B, He M, Chao A, Engelgau MM, Saraiya M, Wang L, Wang L. Cervical Cancer screening among adult women in China, 2010. Oncologist. 2015;20(6):627–34.

    Article  Google Scholar 

  18. Manga MM, Fowotade A, Abdullahi YM, El-Nafaty AU, Adamu DB, Pindiga HU, et al. Epidemiological patterns of cervical human papillomavirus infection among women presenting for cervical cancer screening in north-eastern Nigeria. Infect Agent Cancer. 2015;10:39.

    Article  Google Scholar 

  19. Schiffman M, Doorbar J, Wentzensen N, de Sanjosé S, Fakhry C, Monk BJ. Carcinogenic human papillomavirus infection. Nat Rev Dis Primers. 2016;2(1):16086.

    Article  Google Scholar 

  20. Wentzensen N, Schiffman M, Palmer T, Arbyn M. Triage of HPV positive women in cervical cancer screening. J Clin Virol. 2016;76(Suppl 1):S49–55.

    Article  Google Scholar 

  21. Serrano B, Brotons M, Bosch FX, Bruni L. Epidemiology and burden of HPV-related disease. Best Pract Res Clin Obstet Gynaecol. 2018;47:14–26.

    Article  Google Scholar 

  22. Volpini LPB, Boldrini NAT, de Freitas LB, Miranda AE, Spano LC. The high prevalence of HPV and HPV16 European variants in cervical and anal samples of HIV-seropositive women with normal pap test results. PLoS One. 2017;12(4):e0176422.

    Article  CAS  Google Scholar 

  23. Villa LL, Sichero L, Rahal P, Caballero O, Ferenczy A, Rohan T, Franco EL. Molecular variants of human papillomavirus types 16 and 18 preferentially associated with cervical neoplasia. J Gen Virol. 2000;81(Pt 12):2959–68.

    Article  CAS  Google Scholar 

  24. Altekruse SF, Lacey JV Jr, Brinton LA, Gravitt PE, Silverberg SG, Barnes WA Jr, et al. Comparison of human papillomavirus genotypes, sexual, and reproductive risk factors of cervical adenocarcinoma and squamous cell carcinoma: Northeastern United States. Am J Obstet Gynecol. 2003;188(3):657–63.

    Article  Google Scholar 

  25. Burk RD, Chen Z, Van Doorslaer K. Human papillomaviruses: genetic basis of carcinogenicity. Public Health Genomics. 2009;12(5–6):281–90.

    Article  Google Scholar 

  26. Tan G, Duan M, Li Y, Zhang N, Zhang W, Li B, Qu P. Distribution of HPV 16 E6 gene variants in screening women and its associations with cervical lesions progression. Virus Res. 2019; Nov;273:197740.

    Article  CAS  Google Scholar 

  27. Ortiz-Ortiz J, del C Alarcón-Romero L, Jiménez-López MA, Garzón-Barrientos VH, Calleja-Macías I, Barrera-Saldaña HA, et al. Association of human papillomavirus 16 E6 variants with cervical carcinoma and precursor lesions in women from Southern Mexico. Virol J. 2015;12:29.

    Article  CAS  Google Scholar 

  28. Zuna RE, Tuller E, Wentzensen N, Mathews C, Allen RA, Shanesmith R, et al. HPV16 variant lineage, clinical stage, and survival in women with invasive cervical cancer. Infect Agent Cancer. 2011;6:19.

    Article  Google Scholar 

  29. Alfaro A, Juárez-Torres E, Medina-Martínez I, Mateos-Guerrero N, Bautista-Huerta M, Román-Bassaure E, et al. Different association of human papillomavirus 16 variants with early and late presentation of cervical cancer. PLoS One. 2016;11(12):e0169315.

    Article  CAS  Google Scholar 

  30. Nicolás-Párraga S, Alemany L, de Sanjosé S, Bosch FX, Bravo IG. RIS HPV TT and HPV VVAP study groups differential HPV16 variant distribution in squamous cell carcinoma, adenocarcinoma and adenosquamous cell carcinoma. Int J Cancer. 2017;140(9):2092–100.

    Article  CAS  Google Scholar 

Download references

Acknowledgments

We thank to National Institute of Cancer, Genetic Division, to HPV variants analyses.

Funding

Fundação de Amparo à Pesquisa e ao Desenvolvimento Científico e Tecnológico do Estado do Maranhão (FAPEMA). EDITAL UNIVERSAL-00668/15.

FAPEMA provided financial support for experimental procedures.

Author information

Author notes

  1. Rodrigo Lopes da Silva, Zulmira da Silva Batista, Gerusinete Rodrigues Bastos, Ana Paula Almeida Cunha, Lailson Oliveira de Castro, Liwerbeth dos Anjos Pereira, Marcos Antonio Custódio Neto da Silva, Flávia Castello Branco Vidal, Maria Claudene Barros, Elmary da Costa Fraga, Luciane Maria Oliveira Brito, Maria do Carmo Lacerda Barbosa, Miguel Ângelo Martins Moreira and Maria do Desterro Soares Brandão Nascimento contributed equally to this work.

Authors and Affiliations

  1. Federal University of Maranhão (UFMA), São Luís, Maranhão, Brazil

    Rodrigo Lopes da Silva, Zulmira da Silva Batista, Gerusinete Rodrigues Bastos, Ana Paula Almeida Cunha, Fábio Vidal Figueiredo, Flávia Castello Branco Vidal, Luciane Maria Oliveira Brito, Maria do Carmo Lacerda Barbosa & Maria do Desterro Soares Brandão Nascimento

  2. Faculty of Medicine, Federal University of Maranhão (UFMA), São Luís, Maranhão, Brazil

    Lailson Oliveira de Castro & Liwerbeth dos Anjos Pereira

  3. Faculty of Medical Sciences (FCM), State University of Campinas (UNICAMP), Campinas, São Paulo, Brazil

    Marcos Antonio Custódio Neto da Silva

  4. Center of Advanced Studies of Caxias (CESC), State University of Maranhão (UEMA), Caxias, Maranhão, Brazil

    Maria Claudene Barros & Elmary da Costa Fraga

  5. Genetic Division, National Institute of Cancer (INCA), Rio de Janeiro, Brazil

    Miguel Ângelo Martins Moreira

Authors
  1. Rodrigo Lopes da Silva
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Zulmira da Silva Batista
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Gerusinete Rodrigues Bastos
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Ana Paula Almeida Cunha
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Fábio Vidal Figueiredo
    View author publications

    You can also search for this author in PubMed Google Scholar

  6. Lailson Oliveira de Castro
    View author publications

    You can also search for this author in PubMed Google Scholar

  7. Liwerbeth dos Anjos Pereira
    View author publications

    You can also search for this author in PubMed Google Scholar

  8. Marcos Antonio Custódio Neto da Silva
    View author publications

    You can also search for this author in PubMed Google Scholar

  9. Flávia Castello Branco Vidal
    View author publications

    You can also search for this author in PubMed Google Scholar

  10. Maria Claudene Barros
    View author publications

    You can also search for this author in PubMed Google Scholar

  11. Elmary da Costa Fraga
    View author publications

    You can also search for this author in PubMed Google Scholar

  12. Luciane Maria Oliveira Brito
    View author publications

    You can also search for this author in PubMed Google Scholar

  13. Maria do Carmo Lacerda Barbosa
    View author publications

    You can also search for this author in PubMed Google Scholar

  14. Miguel Ângelo Martins Moreira
    View author publications

    You can also search for this author in PubMed Google Scholar

  15. Maria do Desterro Soares Brandão Nascimento
    View author publications

    You can also search for this author in PubMed Google Scholar

Contributions

RLS, ZSB, GRB, FCBV and MDSBN participated in interpretation of data, drafted and critically revised the manuscript. RLS, MAMM, FVF, ZSB, LMOB, MCLB and MDSBN contributed to study design, interpretation of data, and critically revised the manuscript. MACNS, APAC, LOC and LAP analyzed and assisted in interpretation of the data and assisted in drafting the manuscript. WEMF, DFS, MCB and ECF contributed to interpretation of data and critically revised the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Maria do Desterro Soares Brandão Nascimento.

Ethics declarations

Ethics approval and consent to participate

This project was approved by the Research Ethics Committee of the Federal University of Maranhão (CEP-UFMA), under Consolidated Opinion N° 1.289.419/2015.

All women have signed a written Informed Consent Term to participate of this research.

Consent for publication

All women have signed an Informed Consent Term for data publication.

Competing interests

The authors declare that there are any conflicts of interest in this work.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

da Silva, R.L., da Silva Batista, Z., Bastos, G.R. et al. Role of HPV 16 variants among cervical carcinoma samples from Northeastern Brazil. BMC Women's Health 20, 162 (2020). https://0-doi-org.brum.beds.ac.uk/10.1186/s12905-020-01035-0

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://0-doi-org.brum.beds.ac.uk/10.1186/s12905-020-01035-0

Keywords

BMC Women's Health

ISSN: 1472-6874

Contact us