The site of the Media Sphera Publishers contains materials intended solely for healthcare professionals.
By closing this message, you confirm that you are a certified medical professional or a student of a medical educational institution.

Pakharukova M.I.

Institute of Immunology and Physiology;
Y.B. Beikin Clinical and Diagnostic Center

Yushkov B.G.

Institute of Immunology and Physiology

Comparative analysis of morphometric and histological characteristics of HPV-associated and HPV-independent vulvar squamous cell carcinoma

Authors:

Pakharukova M.I., Yushkov B.G.

More about the authors

Read: 801 times


To cite this article:

Pakharukova MI, Yushkov BG. Comparative analysis of morphometric and histological characteristics of HPV-associated and HPV-independent vulvar squamous cell carcinoma. Russian Journal of Archive of Pathology. 2025;87(3):26‑32. (In Russ.)
https://doi.org/10.17116/patol20258703126

Recommended articles:
Improvement of therapy of papi­llomavirus infe­ction latent forms. Russian Journal of Clinical Dermatology and Vene­reology. 2024;(5):575-580
Immu­nology of the cervix in normal and pathological conditions (literature review). Russian Journal of Human Reproduction. 2024;(5):108-117
Redu­ction of cyto­skeleton gene expression in tumor cells during lentivirus transduction. Mole­cular Gene­tics, Microbiology and Viro­logy. 2025;(1):30-37
Modern methods of treatment of latent form of HPV infe­ction: clinical obse­rvation. Russian Journal of Clinical Dermatology and Vene­reology. 2025;(4):425-429

References:

  1. Bucchi L, Pizzato M, Rosso S, Ferretti S. New insights into the epidemiology of vulvar cancer: systematic literature review for an update of incidence and risk factors. Cancers (Basel). 2022;14(2):389.  https://doi.org/10.3390/cancers14020389
  2. Preti M, Rotondo JC, Holzinger D, Micheletti L, Gallio N, McKay-Chopin S, Carreira C, Privitera SS, Watanabe R, Ridder R, et al. Role of human papillomavirus infection in the etiology of vulvar cancer in Italian women. Infect Agent Cancer. 2020;15:20.  https://doi.org/10.1186/s13027-020-00286-8
  3. WHO Classification of Tumours Editorial Board. WHO Classification of Tumours. Female genital tumours. 5th ed. Vol. 4. Lyon, France; International Agency for Research in Cancer: 2020.
  4. Kortekaas KE, Bastiaannet E, van Doorn HC, de Vos van Steenwijk PJ, Ewing-Graham PC, Creutzberg CL, Akdeniz K, Nooij LS, van der Burg SH, Bosse T, et al. Vulvar cancer subclassification by HPV and p53 status results in three clinically distinct subtypes. Gynecol Oncol. 2020;159(3):649-656.  https://doi.org/10.1016/j.ygyno.2020.09.024
  5. Zhang J, Zhang Y, Zhang Z. Prevalence of human papillomavirus and its prognostic value in vulvar cancer: a systematic review and meta-analysis. PLoS One. 2018;13(9):e0204162. https://doi.org/10.1371/journal.pone.0204162
  6. Rasmussen CL, Sand FL, Frederiksen MF, Andersen KK, Kjaer SK. Does HPV status influence survival after vulvar cancer? Int J Cancer. 2018;142(6):1158-1165. https://doi.org/10.1002/ijc.31139
  7. Cheng AS, Karnezis AN, Jordan S, Singh N, McAlpine JN, Gilks CB. p16 immunostaining allows for accurate subclassification of vulvar squamous cell carcinoma into HPV-associated and HPV-independent cases. Int J Gynecol Pathol. 2016;35(4);385-393.  https://doi.org/10.1097/PGP.0000000000000263
  8. Faber MT, Sand FL, Albieri V. Prevalence and type distribution of human papillomavirus in squamous cell carcinoma and intraepithelial neoplasia of the vulva. Int J Cancer. 2017;141(6):1161-1169. https://doi.org/10.1002/ijc.30821
  9. Rakislova N, Clavero O, Alemany L, Saco A, Quiros B, Lloveras B, Alejo M, Pawlita M, Quint W, Del Pino M, et al.; VVAP study group. Histological characteristics of HPV-associated and -independent squamous cell carcinomas of the vulva: a study of 1594 cases. Int J Cancer. 2017;141(12):2517-2527. https://doi.org/10.1002/ijc.31006
  10. de Sanjosé S, Alemany L, Ordi J, Tous S, Alejo M, Bigby SM, Joura EA, Maldonado P, Laco J, Bravo IG, et al.; HPV VVAP study group. Worldwide human papillomavirus genotype attribution in over 2000 cases of intraepithelial and invasive lesions of the vulva. Eur J Cancer. 2013;49(16):3450-3461. https://doi.org/10.1016/j.ejca.2013.06.033
  11. White EA. Manipulation of epithelial differentiation by HPV oncoproteins. Viruses. 2019;11(4):369.  https://doi.org/10.3390/v11040369
  12. Mittal S, Banks L. Molecular mechanisms underlying human papillomavirus E6 and E7 oncoprotein-induced cell transformation. Mutat Res Rev Mutat Res. 2017; 772: 23-35.  https://doi.org/10.1016/j.mrrev.2016.08.001
  13. Graham SV. Keratinocyte differentiation-dependent human papillomavirus gene regulation. Viruses. 2017;9(9):245.  https://doi.org/10.3390/v9090245
  14. Ershov VA. Concepts of the genesis of hpv-associated cervical cancer. Russian News of Clinical Cytology. 2021;25(1):20-29. (In Russ.). https://doi.org/10.24412/1562-4943-2021-1-0004
  15. Hatterschide J, Bohidar AE, Grace M, Nulton TJ, Kim HW, Windle B, Morgan IM, Munger K, White EA. PTPN14 degradation by high-risk human papillomavirus E7 limits keratinocyte differentiation and contributes to HPV-mediated oncogenesis. Proc Natl Acad Sci USA. 2019;116(14):7033-7042. https://doi.org/10.1073/pnas.1819534116
  16. Zieba S, Chechlinska M, Kowalik A, Kowalewska M. Genes, pathways and vulvar carcinoma — new insights from next-generation sequencing studies. Gynecol Oncol. 2020;158(2):498-506.  https://doi.org/10.1016/j.ygyno.2020.05.034
  17. Singh N, Gilks CB. Vulval squamous cell carcinoma and its precursors. Histopathology. 2020;76(1):128-138.  https://doi.org/10.1111/his.13989
  18. Trietsch MD, Nooij LS, Gaarenstroom KN, van Poelgeest MI. Genetic and epigenetic changes in vulvar squamous cell carcinoma and its precursor lesions: a review of the current literature. Gynecol Oncol. 2015;136(1):143-157.  https://doi.org/10.1016/j.ygyno.2014.11.002
  19. Freije A, Molinuevo R, Ceballos L, Cagigas M, Alonso-Lecue P, Rodriguez R, Menendez P, Aberdam D, De Diego E, Gandarillas A. Inactivation of p53 in human keratinocytes leads to squamous differentiation and shedding via replication stress and mitotic slippage. Cell Rep. 2014;9(4):1349-1360. https://doi.org/10.1016/j.celrep.2014.10.012
  20. Gyöngyösi E, Szalmás A, Ferenczi A, Póliska S, Kónya J, Veress G. Transcriptional regulation of genes involved in keratinocyte differentiation by human papillomavirus 16 oncoproteins. Arch Virol. 2015;160(2):389-398.  https://doi.org/10.1007/s00705-014-2305-y

Email Confirmation

An email was sent to test@gmail.com with a confirmation link. Follow the link from the letter to complete the registration on the site.

Email Confirmation

We use cооkies to improve the performance of the site. By staying on our site, you agree to the terms of use of cооkies. To view our Privacy and Cookie Policy, please. click here.