Int J Med Sci 2020; 17(7):931-938. doi:10.7150/ijms.43030 This issue
1. Institute of Medical Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Kunming 650118, China.
2. School of Basic Medical Science, Kunming Medical University, Kunming 650500, China.
3. Department of Gynaecologic Oncology, The 3rd Affiliated Hospital of Kunming Medical University, Kunming 650118, China.
*These authors contributed equally to this work.
Objective: High-risk human papillomavirus (HPV) E6 and E7 proteins are the major oncoproteins involved in the tumorigenesis of cervical cancer. The long control region (LCR) in HPV plays an important role in regulating the expression of the E6 and E7 oncogenes. In the current study, we investigated the association of HPV16 LCR variations with cervical cancer.
Methods: A total of 139 HPV16-positive cervical cancer patients (case group) and 116 HPV16-positive asymptomatic individuals (control group) were enrolled in the current study. Then, the HPV16 LCR was sequenced to determine the association between LCR variations and cervical cancer.
Results: In the current study, HPV16 A1-A3 (19.4%), A4 (78.4%) and D3 (2.2%) variants were found in the case group. However, only A1-A3 (34.5%) and A4 variants (65.5%) were found in the control group. The distribution of the HPV16 variants between the case and control groups was significantly different (P=0.009). Moreover, a total of eleven variations (A7167G, A7173C, C7176T, C7200T, T7269C, C7286A, C7729A, C7763T, A7841G, G7867A and T24C) were significantly different between the case and control groups (P<0.05). For the sub-lineage analysis, only C7873G variations were significantly different between the case and control groups in the A4 (As) variant (P=0.039).
Conclusion: Our results showed that specific variations in the HPV16 LCR were associated with cervical cancer. Our study will provide a good reference for further understanding of the relationship between HPV16 LCR variation and cervical cancer.
Keywords: Human papillomavirus type 16, LCR, Variations, Cervical cancer, Association
Human papillomavirus (HPV) plays an important role in cervical cancer . HPVs are subdivided according to their oncogenic potential into low-risk and high-risk types . Approximately 15 HPV genotypes (i.e. HPV16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 68, 73, and 82) are recognized as high-risk types, according to an epidemiological survey [3,4], and each type of HPV acts as an independent infection with differing carcinogenic risks . Among the high-risk types, HPV16 is the most common type detected in patients with cervical cancer [5,6].
The HPV genome can be divided into three domains: a long control region (LCR) that contains sequences that control viral transcription and replication, an early region with open reading frames (ORFs) encoding theE1, E2, E4, E5, E6 and E7 genes, and a late region encoding two genes, L1 and L2 [2,7]. The LCR, positioned between the end of the L1 gene and the start of the E6 gene, contains the early p97 promoter, which is responsible for the transcription of E6 and E7 genes and viral DNA replication . Cellular factors play important roles in stimulating and inhibiting p97 promoter activity, such as Oct-1, TEF-1 and YY1. In addition, the viral E2 protein can bind as a dimer to its palindromic recognition sites in the LCR to regulate the expression of E6 and E7 genes [8-14]. The two major viral oncoproteins E6 and E7 play indispensable roles in promoting malignant transformation by targeting the p53 and retinoblastoma protein (pRB) tumour suppressors, respectively [15-18].
HPV16 has coevolved with human kind, and its variants segregate robustly into a phylogenetic tree with four phylogenetic lineages (A, B, C and D) and 16 sub-lineages: A1-A3 variant (previously known as EUR), A4 variant (As), B1-B4 variant (AFR1), C1-C4 variant (AFR2), D1 variant (NA), D2 variant (AA2), D3 variant (AA1) and D4 variant [19,20]. Many studies reported that the carcinogenic capacity is different between sub-lineages, and the non-European lineages have stronger pathogenicity in developing cervix cancer in comparison with European lineages, such as the D3 variant (AA1) and A4 variant (As) [19,21]. In addition to the HPV16 variants, viral genetic variations could play a vital role in cervical carcinogenesis [14,22-25]. For example, the T variation of the E6 gene T350G (L83V) persisted more often than the G variation in the EUR sub-lineage .
Our previous study also showed that the HPV16 variants and the variations in theE1, E2, E6 and E7 genes were associated with cervical cancer in the Chinese Han population [26-28].Thus, in the current study, we investigated the distribution of LCR variation in the HPV16-positive asymptomatic individuals and HPV16-positive cervical cancer patients and found an association between the LCR variations and cervical cancer in a Han Chinese population.
All procedures were in accordance with the ethical standards of the responsible committee on human experimentation and with the Helsinki Declaration of 1964, which was revised in 2013. All experimental protocols were approved by the Institutional Review Boards of the No. 3 Affiliated Hospitals of Kunming Medical University. All participants provided written informed consent.
In the current study, the case group included 139 HPV16-positive cervical cancer patients, and 116 HPV16-positive asymptomatic individuals undergoing routine health check-ups were recruited as the control group. All individuals were recruited at the 3rd Affiliated Hospital of Kunming Medical University from 2017 to 2019. The sample type analysed inthe case group was cervical cancer tissues, and the sample type analysedin the control group was cervical exfoliated cells. The inclusion criteria: the patients were diagnosed according to “Diagnosis and Treatment Obstetrics and Gynaecology” and International Federation of Gynaecology and Obstetrics, 2009; the patients were not suffering from other malignancies; and the patients had not received chemotherapy and radiotherapy. The exclusion criteria were as follows: patients with prior malignant tumour history except cervical cancer; patients receiving radiotherapy or chemotherapy; and patients with an unclear pathological diagnosis. Over the same period, the healthy HPV16-positive asymptomatic women undergoing the healthy routine screen at the same hospital served as the healthy controls in the current study. All participants were self-reported as ethnically Han in the current study.
For HPV genotyping, the Tellgenplex™ HPV DNA Test, which is a suspension bead array method for identifying HPV types, was used. The experimental protocol has been described in a previous study . Human β-globin was used as an internal control for each reaction.
The HPV16 LCR was amplified using a high-fidelity DNA polymerase with the primers 5'-TACCTCTACAACTGCTAAACGC-3' and 5'-CCTGTGGGTCCTGAAACA-3' (912 bp); the PCR product contained the complete LCR sequence, with a length of 832 bp, and the reference sequence used was AF534061.1. PCR was performed in a final volume of 25 μl, and each PCR mixture contained 1× Q5 PCR buffer (containing Mg2+), 200 μM dNTPs, 0.5 μM sense and antisense primers, 50 ngof genomic DNA, and 0.02 U/μl high-fidelity DNA polymerase. The PCR conditions were as follows: an initial denaturation step at 98°C for 3 min, 35 cycles of denaturation at 98°C for 10 s, annealing at 60°C for 30 s, and extension at 72°C for 90 s; and a final elongation at 72°C for 2 min. The amplified DNA fragments (including the complete LCR sequence) were sent to Shanghai Sangon Biotech for sequencing after visualization with a 1.0% agarose electrophoresis assay. The primers used for LCR sequencing were 5'-AATCCCTGTTTTCCTGACCTG-3', 5'-CAAGCCAAAAATATGTGCCTAAC-3'.
All sequences of the HPV16 LCR sequences were assembled by SeqMan software and aligned by the ClustalW multiple sequence alignment tool included in the Molecular Evolutionary Genetics Analysis (MEGA) v7.0 software package. The HPV16 reference sequence AF534061.1 was used to identify variations in the HPV16 LCR sequences. Phylogenetic trees of the HPV16 LCR were constructed using MEGA 7.0 software by the maximum likelihood method by bootstrapping with 1000 replications. The reference sequences used to construct the phylogenetic tree were obtained from GenBank, and the accession numbers are HQ644283.1 (A1), HQ644268.1 (A1), HQ644280.1 (A1), HQ644282.1 (A1), AF536179.1 (A2), HQ644236.1 (A3), HQ644248.1 (A4), HQ644251.1 (A4), AF534061.1 (A4), HQ644235.1 (A4), HQ644240.1 (B1), HQ644290.1 (B1), HQ644238.1 (B1), HQ644298.1 (B3), HQ644237.1 (C), HQ644239.1 (C), HQ644249.1 (C), HQ644250.1 (C), AF472509.1 (C), HQ644257.1 (D1), HQ644279.1 (D2), HQ644281.1 (D2), HQ644263.1 (D2), HQ644277.1 (D2), HQ644247.1 (D3), HQ644253.1 (D3), HQ644255.1 (D3), and AF402678.1 (D3).
The frequency of each HPV16 LCR variation was determined by direct counting. A chi-square test, Fisher's exact test or continuity correction test was performed to analyse the associations of HPV16 LCR variations with cervical cancer. The statistical analyses were performed using SPSS 13 (Chicago, IL), and P values less than 0.05 were considered statistically significant.
In the current study, there were three HPV16 sub-lineages in the case group, namely, A1-A3 (EUR), A4 (As) and D3 (AA1), with distribution frequencies of 19.4%, 78.4% and 2.2%, respectively (Figure 1). In the control group, only the A1-A3 (EUR) and A4 (As) sub-lineages were found, with distribution frequencies of 34.5% and 65.5%, respectively (Figure 2). The difference in the distribution of the HPV16 variants between the case group and control group was statistically significant (P=0.009).
The HPV16 LCR variations in the case and control groups are shown in Table 1 (Reference sequence AF534061.1). Thirty-nine variations were observed in the case group, and thirty-two variations were observed in the control group. Among these variations, a total of eleven variations (A7167G, A7173C, C7176T, C7200T, T7269C, C7286A, C7729A, C7763T, A7841G, G7867A and T24C) were statistically significant between the case group and control group (P<0.05).
HPV16 LCR variations in the case and control groups
|HPV16 LCR segment||HPV16 Genome position||Case (n=139)||Control (n=116)||P Value|
|Variation||Frequency (%)||Variation||Frequency (%)|
Note: The reference HPV16 LCR sequence used was AF534061.1. a Pearson Chi-Square; b Continuity Correction; c Fisher's Exact Test.
The phylogenetic tree based on the HPV16 LCR sequences from HPV16-positive cervical cancer patients, corresponding to the AF534061.1 reference sequence (nucleotide positions 7156-7905, 1-82).
The phylogenetic tree based on the HPV16 LCR sequences from HPV16-positive asymptomatic individuals, corresponding to the AF534061.1 reference sequence (nucleotide positions 7156-7905, 1-82).
HPV16LCR variations in the case and control groups in A1-A3, A4 and D3 sub-lineages
|Genome position||A1-A3-Case (n=27)||A1-A3-Control (n=40)||P Value||A4-Case (n=109)||A4-Control (n=76)||P Value||D3-Case (n=3)|
|Variation||Frequency (%)||Variation||Frequency (%)||Variation||Frequency (%)||Variation||Frequency (%)||Variation||Frequency (%)|
Note: The reference HPV16 LCR sequence used was AF534061.1. a Pearson Chi-Square; b Continuity Correction; c Fisher's Exact Test.
Table 2 shows HPV16 LCR gene variations in the A1-A3 (EUR), A4 (As) and D3 (AA1) sub-lineages. A total of eighteen and twenty-three variations were found in the case and control group in the A1-A3 (EUR) variants, respectively, and no variations were significantly different between the case and control group (P>0.05). However, A7173C showed a trend to associate with cervical cancer (P=0.074) in the A1-A3 (EUR) variants (case: 0% vs control: 15%). In the HPV16 A4 (As) variant, fifteen and thirteen variations were found in the case and control groups, respectively. The C7873G variation was significantly different between the case (8.3%) and control (18.4%) group (P=0.039), and the A7232C showed a trend to associate with cervical cancer (case: 0% vs control: 3.9%; P=0.068) in the HPV16 A4 (As) variant.
The HPV16 LCR contains the transcriptional enhancer and promoter regions as well as the origin of DNA replication. The LCR variations can have various transcriptional activities by changing the activity of the promoter [8-14]. In the current study, we investigated the distribution of LCR variation in HPV16-positive asymptomatic individuals and HPV16-positive cervical cancer patients. Our results showed that the distribution of the HPV16 variants and variations in LCR were associated with the development of cervical cancer.
Previous studies have indicated that HPV16 variants have different carcinogenic potentials [30-32]. In the current study, we found that the frequencies of the A4 (As) variant were significantly different between the case and control groups (78.4% vs 65.5%, respectively). We also found that the D3 (AA1) variant was only found in the case group (2.2%). These results were concordant with our previous finding and other studies showing that non-A1-A3 (non-EUR), such as A4 (As) and D3 (AA1) variants, could have a higher risk of progression to cervical cancer than A1-A3 (EUR) variants [14,26,28,33-36]. The reason for these differences could be that HPV intratypic variants have various transcriptional activities that alter biological and biochemical properties and lead to differences in the pathogenicity of these variants .
Previous studies have reported that HPV-16 LCR E2 binding sites serve as landmarks to divide the LCR into functionally distinct segments, which have been called the 5', the central, and the 3′ segment of LCR . The 5' segment of the HPV16 LCR has a size of approximately 300 bp and is bracketed by the termination codon of L1 and the first E2 binding site (7455 site) . The 5' segment of HPV16 LCR contains a transcription termination site and a negative regulatory element acting at the level of late mRNA stability [36,48]. In the current study, the distributions of A7167G and A7173C were located in the 5' segment of the LCR of HPV16, and our results showed that the distributions of the two variations were significantly different between the case and control groups (P=0.007 and P=0.008, respectively). Connor et al. and Xi et al. reported that A7167G and A7173C are located in the binding site of the transcription factor AP1 and FOXA1 [12,13]. FOXA1 acts as a key transcription factor to regulate the progression of cancer in different cancers, such as breast, liver and lung cancer [38-42]. For AP1, one of the AP1 roles could translate increased mitogenic signals into increased levels of viral gene transcription through E5 action . The other role could be that AP1 mediates the repressive effect of retinoids, which are the molecular antagonists to AP1 , on HPV gene expression . Thus, these two variations could change the binding of transcription factors to play an important role in E6 and E7gene expression.
The central segment of the HPV16 LCR is flanked by two E2 protein binding sites (7455and 7862), which have a size of approximately 400 bp . The central segment of the HPV16 LCR is an epithelial-specific transcriptional enhancer region that has many transcription factor binding sites and plays an important role in the regulation of the gene expression ofE6 and E7 [46,47]. In the current study, we found that the frequencies of C7729A, C7763T and A7841G, which are located in the enhancer region, showed significant differences between the case and control groups (P=0.033, 0.017, and 0.022, respectively). C7729A is located in the enhancer region and proximal to the binding site of YY1, NF1, Tef-1 and Octamer factor-1 transcription factors [8,12,14]. Although C7763T and A7841G were not located in the enhancer region, these two sites are close to the enhancer region and the binding sites of NF1 and YY1, respectively [8,12,14]. Several studies have reported that YY1, NFI, TEF-1 and Octamer factor-1 have roles in viral replication, regulate viral and cellular genes and influence enhancer activity [48-52]. Thus, these variations could change the binding of transcription factors to influence E6 and E7 gene expression.
The 3' segment of the HPV16 LCR was between the second E2 protein binding site (7862) and the E6 gene and has a size of approximately 140 bp . Several studies have reported that variations in the p97 promoter, which is located in the E6 gene proximal part of the LCR, could influence the transcription of E6 and E7 genes. In the current study, we found that the distribution of T24C showed a significant difference between the control and case groups (P=0.043), which indicated that this variation could induce dysregulation of E6 and E7 gene expression through changing the cellular and viral transcription factor binding sites. In 2013, Pientong et al. found that G7428A and C7873G in the A4 (As) variant, which are proximal to the p97 promoter, showed higher transcriptional activity than other A4 (As) and A1-A3 (EUR) variants . In the current study, our results also showed that the distribution of C7873G was significantly different between the case and control groups in the A4 (As) variant (P=0.039). These results indicated that the oncogenic potential of the A4 (As) variant could be influenced by variations that are proximal to the promoter region.
The viral E2 protein, which binds as a dimer to LCR recognition sites, is considered a negative regulator by repressing or activating the expression of E6 and E7 genes . In the current study, G7867A variation, which is likely one of the binding sites of E2 protein, was only found in the control group. This variation could play a role in the occurrence of cervical cancer by affecting the binding efficiency of the HPV16 E2 protein.
One of the limitations in the current study was that our data only presented the case-control study results and there was a lack of functional validation that would allow for a closer understanding of the relationship between intratypic variation and the carcinogenic potential of the most frequent high-risk HPV genotypes. In the future, we will do the variations function validation to find the role of the viral genetic variability in the different courses of HPV-associated diseases.
In the current study, our results showed that the distribution of the HPV16 variants was significantly different between the case group and control groups, and D3 (AA1) was only found in the case group. In addition, we also found that HPV16 LCR variations (A7167G, A7173C, C7176T, C7200T, T7269C, C7286A, C7729A, C7763T, A7841G, G7867A and T24C) were statistically significant between the case group and control groups. Moreover, the distribution of C7873G variation was significantly different between the case and control groups in the A4 (As) variant, and no variations were significantly different between the case and control groups in the A1-A3 (EUR) variant.
This work was supported by grants from the National Science Foundation of China (81573206), Yunnan Applied Basic Research Projects (2016FA034), Fundamental Research Funds for the Central Universities and the PUMC Youth Fund (3332015149 and 3332019111), The Association Foundation Program of Yunnan Provincial Science and Technology Department and Kunming Medical University (2017FE467-012, -077 and -125) and Special Funds for high-level health talents of Yunnan Province (D-201669 and L-201615). The funders had no role in study design, data collection and analysis, decision to publish or preparation of the manuscript.
The authors have declared that no competing interest exists.
1. Groves IJ, Coleman N. Pathogenesis of human papillomavirus-associated mucosal disease. J Pathol. 2015;235:527-38
2. Stanley MA, Pett MR, Coleman N. HPV: from infection to cancer. Biochem Soc Trans. 2007;35:1456-60
3. Munoz N, Bosch FX, de Sanjose S, Herrero R, Castellsague X, Shah KV. et al. Epidemiologic classification of human papillomavirus types associated with cervical cancer. N Engl J Med. 2003;348:518-27
4. Schiffman M, Castle PE, Jeronimo J, Rodriguez AC, Wacholder S. Human papillomavirus and cervical cancer. Lancet. 2007;370:890-907
5. de Sanjose S, Quint WG, Alemany L, Geraets DT, Klaustermeier JE, Lloveras B. et al. Human papillomavirus genotype attribution in invasive cervical cancer: a retrospective cross-sectional worldwide study. Lancet Oncol. 2010;11:1048-56
6. Cho HW, So KA, Lee JK, Hong JH. Type-specific persistence or regression of human papillomavirus genotypes in women with cervical intraepithelial neoplasia 1: A prospective cohort study. Obstet Gynecol Sci. 2015;58:40-5
7. Burk RD, Chen Z, Van Doorslaer K. Human papillomaviruses: genetic basis of carcinogenicity. Public Health Genomics. 2009;12:281-90
8. Kammer C, Warthorst U, Torrez-Martinez N, Wheeler CM, Pfister H. Sequence analysis of the long control region of human papillomavirus type 16 variants and functional consequences for P97 promoter activity. J Gen Virol. 2000;81:1975-81
9. Veress G, Szarka K, Dong XP, Gergely L, Pfister H. Functional significance of sequence variation in the E2 gene and the long control region of human papillomavirus type 16. J Gen Virol. 1999;80( Pt 4):1035-43
10. Kurvinen K, Yliskoski M, Saarikoski S, Syrjanen K, Syrjanen S. Variants of the long control region of human papillomavirus type 16. Eur J Cancer. 2000;36:1402-10
11. Veress G, Murvai M, Szarka K, Juhasz A, Konya J, Gergely L. Transcriptional activity of human papillomavirus type 16 variants having deletions in the long control region. Eur J Cancer. 2001;37:1946-52
12. Connor MO, Chan SY, Bernard HU. Transcription Factor Binding Sites in the Long Control Region of Genital HPVs. ''Human Papillomaviruses. 1995 Compendium'' (G Myers, Ed), III-A,. 1995: pp. 21-40. Los Alamos, NM
13. Xi J, Chen J, Xu M, Yang H, Luo J, Pan Y. et al. Genetic variability and functional implication of the long control region in HPV-16 variants in Southwest China. PLoS One. 2017;12:e0182388
14. Pientong C, Wongwarissara P, Ekalaksananan T, Swangphon P, Kleebkaow P, Kongyingyoes B. et al. Association of human papillomavirus type 16 long control region mutation and cervical cancer. Virol J. 2013;10:30
15. Dyson N, Howley PM, Munger K, Harlow E. The human papilloma virus-16 E7 oncoprotein is able to bind to the retinoblastoma gene product. Science. 1989;243:934-7
16. Scheffner M, Werness BA, Huibregtse JM, Levine AJ, Howley PM. The E6 oncoprotein encoded by human papillomavirus types 16 and 18 promotes the degradation of p53. Cell. 1990;63:1129-36
17. Crook T, Tidy JA, Vousden KH. Degradation of p53 can be targeted by HPV E6 sequences distinct from those required for p53 binding and trans-activation. Cell. 1991;67:547-56
18. Boyer SN, Wazer DE, Band V. E7 protein of human papilloma virus-16 induces degradation of retinoblastoma protein through the ubiquitin-proteasome pathway. Cancer Res. 1996;56:4620-4
19. Burk RD, Harari A, Chen Z. Human papillomavirus genome variants. Virology. 2013;445:232-43
20. Mirabello L, Clarke MA, Nelson CW, Dean M, Wentzensen N, Yeager M. et al. The Intersection of HPV Epidemiology, Genomics and Mechanistic Studies of HPV-Mediated Carcinogenesis. Viruses. 2018 10
21. Mirabello L, Yeager M, Cullen M, Boland JF, Chen Z, Wentzensen N. et al. HPV16 Sublineage Associations With Histology-Specific Cancer Risk Using HPV Whole-Genome Sequences in 3200 Women. J Natl Cancer Inst. 2016 108
22. Cornet I, Gheit T, Clifford GM, Combes JD, Dalstein V, Franceschi S. et al. Human papillomavirus type 16 E6 variants in France and risk of viral persistence. Infect Agent Cancer. 2013;8:4
23. Kirnbauer R, Taub J, Greenstone H, Roden R, Durst M, Gissmann L. et al. Efficient self-assembly of human papillomavirus type 16 L1 and L1-L2 into virus-like particles. J Virol. 1993;67:6929-36
24. Pillai MR, Hariharan R, Babu JM, Lakshmi S, Chiplunkar SV, Patkar M. et al. Molecular variants of HPV-16 associated with cervical cancer in Indian population. Int J Cancer. 2009;125:91-103
25. Mosmann JP, Monetti MS, Frutos MC, Kiguen AX, Venezuela RF, Cuffini CG. Mutation detection of E6 and LCR genes from HPV 16 associated with carcinogenesis. Asian Pac J Cancer Prev. 2015;16:1151-7
26. Dai S, Yao Y, Yan Z, Zhou Z, Shi L, Wang X. et al. The association of human papillomavirus type 16 E2 variations with cervical cancer in a Han Chinese population. Infect Genet Evol. 2018;64:241-8
27. Yao Y, Yan Z, Dai S, Li C, Yang L, Liu S. et al. Human Papillomavirus Type 16 E1 Mutations Associated with Cervical Cancer in a Han Chinese Population. Int J Med Sci. 2019;16:1042-9
28. Zhou Z, Yang H, Yang L, Yao Y, Dai S, Shi L. et al. Human papillomavirus type 16 E6 and E7 gene variations associated with cervical cancer in a Han Chinese population. Infect Genet Evol. 2019;73:13-20
29. Li WJ, Xu HX, Chen ZH, Xu WD, Wu YJ. Characteristics of carcinogenic human papillomavirus infection in Suzhou: Epidemiology, vaccine evaluation, and associated diseases. J Med Virol. 2017;89:895-901
30. 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 Biomarkers Prev. 2007;16:4-10
31. Perez S, Cid A, Inarrea A, Pato M, Lamas MJ, Couso B. et al. Prevalence of HPV 16 and HPV 18 lineages in Galicia, Spain. PLoS One. 2014;9:e104678
32. Sichero L, Ferreira S, Trottier H, Duarte-Franco E, Ferenczy A, Franco EL. et al. High grade cervical lesions are caused preferentially by non-European variants of HPVs 16 and 18. Int J Cancer. 2007;120:1763-8
33. Chan PK, Lam CW, Cheung TH, Li WW, Lo KW, Chan MY. et al. Human papillomavirus type 16 intratypic variant infection and risk for cervical neoplasia in southern China. J Infect Dis. 2002;186:696-700
34. Lee CW, Bae JH, Lee SJ, Ho EM, Lee IH, Park YG. et al. Distribution of human papillomavirus type 16 E6 and E7 gene variants in the progression of cervical dysplasia in Korean women. J Obstet Gynaecol Res. 2011;37:1320-6
35. Chopjitt P, Ekalaksananan T, Pientong C, Kongyingyoes B, Kleebkaow P, Charoensri N. Prevalence of human papillomavirus type 16 and its variants in abnormal squamous cervical cells in Northeast Thailand. Int J Infect Dis. 2009;13:212-9
36. Wu Y, Chen Y, Li L, Yu G, He Y, Zhang Y. Analysis of mutations in the E6/E7 oncogenes and L1 gene of human papillomavirus 16 cervical cancer isolates from China. J Gen Virol. 2006;87:1181-8
37. Giannoudis A, Herrington CS. Human papillomavirus variants and squamous neoplasia of the cervix. J Pathol. 2001;193:295-302
38. Cowper-Sal lari R, Zhang X, Wright JB, Bailey SD, Cole MD, Eeckhoute J. et al. Breast cancer risk-associated SNPs modulate the affinity of chromatin for FOXA1 and alter gene expression. Nat Genet. 2012;44:1191-8
39. Li Z, Tuteja G, Schug J, Kaestner KH. Foxa1 and Foxa2 are essential for sexual dimorphism in liver cancer. Cell. 2012;148:72-83
40. Jin HJ, Zhao JC, Ogden I, Bergan RC, Yu J. Androgen receptor-independent function of FoxA1 in prostate cancer metastasis. Cancer Res. 2013;73:3725-36
41. Lin L, Miller CT, Contreras JI, Prescott MS, Dagenais SL, Wu R. et al. The hepatocyte nuclear factor 3 alpha gene, HNF3alpha (FOXA1), on chromosome band 14q13 is amplified and overexpressed in esophageal and lung adenocarcinomas. Cancer Res. 2002;62:5273-9
42. Wang J, Bao W, Qiu M, Liao Y, Che Q, Yang T. et al. Forkhead-box A1 suppresses the progression of endometrial cancer via crosstalk with estrogen receptor alpha. Oncol Rep. 2014;31:1225-34
43. Leechanachai P, Banks L, Moreau F, Matlashewski G. The E5 gene from human papillomavirus type 16 is an oncogene which enhances growth factor-mediated signal transduction to the nucleus. Oncogene. 1992;7:19-25
44. Fanjul A, Dawson MI, Hobbs PD, Jong L, Cameron JF, Harlev E. et al. A new class of retinoids with selective inhibition of AP-1 inhibits proliferation. Nature. 1994;372:107-11
45. Bartsch D, Boye B, Baust C, zur Hausen H, Schwarz E. Retinoic acid-mediated repression of human papillomavirus 18 transcription and different ligand regulation of the retinoic acid receptor beta gene in non-tumorigenic and tumorigenic HeLa hybrid cells. EMBO J. 1992;11:2283-91
46. Cripe TP, Haugen TH, Turk JP, Tabatabai F, Schmid PG 3rd, Durst M. et al. Transcriptional regulation of the human papillomavirus-16 E6-E7 promoter by a keratinocyte-dependent enhancer, and by viral E2 trans-activator and repressor gene products: implications for cervical carcinogenesis. EMBO J. 1987;6:3745-53
47. Gloss B, Bernard HU, Seedorf K, Klock G. The upstream regulatory region of the human papilloma virus-16 contains an E2 protein-independent enhancer which is specific for cervical carcinoma cells and regulated by glucocorticoid hormones. EMBO J. 1987;6:3735-43
48. Ruvkun G, Finney M. Regulation of transcription and cell identity by POU domain proteins. Cell. 1991;64:475-8
49. Ishiji T, Lace MJ, Parkkinen S, Anderson RD, Haugen TH, Cripe TP. et al. Transcriptional enhancer factor (TEF)-1 and its cell-specific co-activator activate human papillomavirus-16 E6 and E7 oncogene transcription in keratinocytes and cervical carcinoma cells. EMBO J. 1992;11:2271-81
50. Tjian R, Maniatis T. Transcriptional activation: a complex puzzle with few easy pieces. Cell. 1994;77:5-8
51. Bauknecht T, Angel P, Royer HD, zur Hausen H. Identification of a negative regulatory domain in the human papillomavirus type 18 promoter: interaction with the transcriptional repressor YY1. EMBO J. 1992;11:4607-17
52. Bauknecht T, Jundt F, Herr I, Oehler T, Delius H, Shi Y. et al. A switch region determines the cell type-specific positive or negative action of YY1 on the activity of the human papillomavirus type 18 promoter. Journal of Virology. 1995;69:1
53. Thierry F. Transcriptional regulation of the papillomavirus oncogenes by cellular and viral transcription factors in cervical carcinoma. Virology. 2009;384:375-9
Corresponding authors: Dr. Li Shi, Institute of Medical Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Kunming 650118, China, E-mail address: shili.imbcom. AND Dr. Yufeng Yao, Institute of Medical Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Kunming 650118, China, E-mail address: yufeng_yaocom.cn or leoyyfcom.