Human papillomavirus 16 physical status detection in preinvasive and invasive cervical carcinoma by multiplex real-time polymerase chain reaction
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  • 作者:Ying Zheng (1)
    Zhilan Peng (1)
    Jiangyan Lou (1)
    He Wang (1)
  • 关键词:HPV ; multiplex real ; time polymerase chain reaction ; integration ; cervical carcinoma
  • 刊名:The Chinese-German Journal of Clinical Oncology
  • 出版年:2007
  • 出版时间:February 2007
  • 年:2007
  • 卷:6
  • 期:1
  • 页码:72-79
  • 全文大小:472KB
  • 参考文献:1. Badaracco G, Venuti A, Sedati A, / et al. HPV-16 and HPV-18 in genital tumors: significantly different levels of viral integration and correlation to tumor invasiveness. J Med Virol, 2002, 67: 574鈥?82. CrossRef
    2. Francis DA, Schmid SI, Howley PM. Repression of the integrated papillomavirus E6/E7 promotor is required for growth suppression of cervical cancer cells. J Virol 2000, 74: 2679鈥?686. CrossRef
    3. Romanczuk H, Thierry F, Howley PM. Mutational analysis of cis elements involved in E2 modulation of human papillomavirus type 16 P97 and type 18 P105 promotors. J Virol, 1990, 64: 2849鈥?859.
    4. Panu P, Bo J, Stina S. Integrated human papillomavirus type 16 is frequently found in cervical cancer precursors as demonstrated by a novel quantitative real-time PCR technique. J Clin Microbiology, 2002, 40: 886鈥?91. CrossRef
    5. Gallo G, Bibbo M, Bagella L. / et al. Study of viral integration of HPV-16 in young patients with LSIL. J Clin Pathol, 2003, 56: 532鈥?36. CrossRef
    6. Kalantari M, Karlsen F, Kristensen G, / et al. Disruption of the E1 anf E2 reading frames of HPV-16 in cervical carcinoma is associated with poor prognosis. Int J Gynecol Pathol, 1998, 17: 146鈥?53. CrossRef
    7. Southern EM. Detection of specific sequences among DNA fragments separated by gel electrophoresis. J Mol Biol, 1975, 98: 503鈥?17. CrossRef
    8. Heid CA, Stevens J, Livak KJ, / et al. Real time quantitative PCR. Genome Res, 1996, 6: 986鈥?94.
    9. von Kenebel Doeberitz M, Rittmuller C, Aengeneyndt F, / et al. Reversible repression of papillomavirus oncogene expression in cervical carcinoma cells: consequences for the phenotype and E6-p53 and E7-pRB interactions. J Virol, 1994, 68: 2811鈥?821.
    10. Jeon S, Allen-Hoffmann BL, Lambert PF. Integration of human papillomavirus type 16 into the human genome correlates with a selective growth advantage of cells. J Virol, 1995, 69: 2989鈥?997.
    11. Sang BC, Barbosa MS. Increased E6/E7 transcription in HPV 18-immortalized human keratinocytes results from inactivation of E2 and additional cellular events. Virology, 1992, 189: 448鈥?55. CrossRef
    12. Cullen AP, Reid R, Campion M, / et al. Analysis of physical state of different human papillomavirus DNAs in intraepithelial and invasive cervical neoplasms. J Virol, 1991, 65: 606鈥?12.
    13. Das BC, Sharma JK, Luthra GK, / et al. Analysis by polymerase chain reaction of the physical state of human papillomavirus type 16 DNA in cervical preneoplastic and neoplastic lesions. J Gen Virol, 1992, 73: 2327鈥?336.
    14. Daniel B, Rangarajan A, Mukherjee G, / et al. The link between integration and expression of human papillomavirus type 16 genomes and cellular changes in the evolution of cervical intraepithelial neoplastic lesions. J Gen Virol, 1997, 78: 1095鈥?101.
    15. Syrj盲nen K, Syrj盲ner S. Papillomavirus infections in human pathology. New York: J Wiley & Sons Ltd., 2000.
    16. Romanzuk H, Howley P. Disruption of either the E1 and E2 regulatory gene of human papillomavirus type 16 increases viral immortalization capacity. Proc Natl Acad Sci USA, 1992, 89: 3159鈥?163. CrossRef
    17. Awady MK, Kaplan JB, Obrien SJ, / et al. Molecular analysis of integrated human papillomvirus 16 sequences in the cervical cancer cell line SiHa. Virology, 1987, 159: 389鈥?98. CrossRef
    18. Park J, Hwang E, Park S, / et al. Physical status and expression of HPV genes in cervical cancers. Gynecol Oncol, 1997, 65: 121鈥?29. CrossRef
    19. Ylitalo N, Josefsson A, Melbye M, / et al. Aprospective study showing long-term infection with human papillomavirus 16 before the development of cervical carcinoma in situ. Cancer Res, 2000, 60: 6027鈥?032.
    20. Vernon SD, Unger ER, Miller DL, / et al. Association of human papillomavirus type 16 integration in the E2 gene with poor disease-free survival from cervical cancer. Int J Cancer, 1997, 74: 50鈥?6. CrossRef
    21. Howley PM. Presence and expression of human papillomavirus sequences in human cervical carcinoma cell lines. Am J Pathol, 1985, 119: 361鈥?66.
    22. zur Hausen H. Papillomavirus causing cancer: evasion from host-cell control in early events in carcinogenesis. J Natl Cancer Inst, 2000, 92: 690鈥?98. CrossRef
    23. Daniel B, Mukherjee G, Seshadri L, / et al. Changes in the physical state and expression of human papillomavirus type 16 in the pregression of cervical intraepithelial neoplasia lesions analysed by PCR. J Gen Virol, 1995, 76: 2589鈥?593. CrossRef
    24. Sastre-Garau X, Schneider-Maunoury S, Couturier J, / et al. Human papillomavirus type 16 DNA is integrated into chromosome region 12q14-q15 in a cell line derived from a vulvar intraepithelial neoplasia. Cancer Genet Cytogenet, 1990, 44: 243鈥?51. CrossRef
    25. Matsukura T, Koi S, Sugase M. Both episomal and integrated forms of human papillomavirus type 16 are involved in invasive cervical cancers. Virology, 1989, 172: 63鈥?2. CrossRef
    26. Fuchs PG, Girardi F, Pfister H. Human papillomavirus 16 DNA in cervical cancers and lymph nodes of cervical cancer patients: a diagnostic marker for early metastases? Int J Cancer, 1989, 43: 41鈥?4. CrossRef
    27. Wentzensen N, Vinokurova S, von KnebelDoeberitz. Systematic review of genomic integration sites of human papillomavirus genomes in epithelial dysplasia and invasive cancer of the female lower genital tract. Cancer Res, 2004, 64: 3878鈥?884. CrossRef
    28. Unger ER, Vernon SD, Thoms WW, / et al. Human papillomavirus and disease-free survival from cervical cancer. Int J Cancer, 1997, 74: 50鈥?6. CrossRef
    29. Zoltan H, Krisztina S, Tamas S, / et al. The prognostic significance of HPV-16 genome status of the lymph nodes, the integration status and p53 genotype in HPV-16 positive cervical cancer: a long term follow up. Br J Obstet Gynaecol, 2003, 110: 205鈥?09.
  • 作者单位:Ying Zheng (1)
    Zhilan Peng (1)
    Jiangyan Lou (1)
    He Wang (1)

    1. Department of Obstetrics and Gynecology, West China Second University Hospital, Sichuan University, Chengdu, 610041, China
文摘
Objective To explore an ideal approach for detecting the physical status of HPV-16 in clinic use and to investigate the integrated HPV-16 in CINs and cervical cancer. Methods Multiplex real-time PCR method was established to quantify the copy numbers of E2 and E6 genes (E2/E6) for analysis of the physical status of HPV-16 DNA and this assay was compared to Southern blot analysis. HPV-16-containing paraffin-embedded tissues including 49 CINs and 51 cervical squamous cancers were detected using the method. Results (1) The cutoff ratio of E2/E6 to distinguish pure episomal from mixed HPV-16, was 0.81 in the multiplex real-time PCR; (2) The agreement rate between multiplex real-time PCR and Southern blot was 81.5% (the Kappa statistic was 0.844, P<0.001); (3) HPV-16 DNA existed in an episomal form in 57.1% and mixed form in 42.9% of CIN I lesions; The concomitant form of HPV-16 (>70%) constituted the majority in CIN II and CIN III; HPV-16 DNA mostly integrated into the host chromosome (s) in squamous cervical cancers (68.6%); (4) The incidence of HPV-16 integration was increased with the degree of cervical lesions; (5) The frequency of pure integrated HPV-16 in stage II+III (88%) was significantly higher than that in stage I (33.3%). Conclusion (1) Mutiplex real-time PCR provides a rapid, sensitive and reliable method for clinic detection of the physical state of HPV-16 DNA; (2) The integration of the HPV-16 DNA is a very early and important event in the progression from preinvasive to invasive cervical cancer; (3) The pure integrated status of HPV-16 in cervical cancer may be associated with poor prognosis of cervical cancer, but further study will be needed to prove its prognostic significance.

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