Differential expression of human papillomavirus 16-, 18-, 52-, and 58-derived transcripts in cervical intraepithelial neoplasia

Virol J. 2020 Mar 6;17(1):32. doi: 10.1186/s12985-020-01306-0.

Abstract

Background: Human papillomavirus (HPV) infection is a primary cause of cervical cancer. Although epidemiologic study revealed that carcinogenic risk differs according to HPV genotypes, the expression patterns of HPV-derived transcripts and their dependence on HPV genotypes have not yet been fully elucidated.

Methods: In this study, 382 patients with abnormal cervical cytology were enrolled to assess the associations between HPV-derived transcripts and cervical intraepithelial neoplasia (CIN) grades and/or HPV genotypes. Specifically, four HPV-derived transcripts, namely, oncogenes E6 and E6*, E1^E4, and viral capsid protein L1 in four major HPV genotypes-HPV 16, 18, 52, and 58-were investigated.

Results: The detection rate of E6/E6* increased with CIN progression, whereas there was no significant change in the detection rate of E1^E4 or L1 among CIN grades. In addition, we found that L1 gene expression was HPV type-dependent. Almost all HPV 52-positive specimens, approximately 50% of HPV 58-positive specimens, around 33% of HPV 16-positive specimens, and only one HPV18-positive specimen expressed L1.

Conclusions: We demonstrated that HPV-derived transcripts are HPV genotype-dependent. Especially, expression patterns of L1 gene expression might reflect HPV genotype-dependent patterns of carcinogenesis.

Keywords: Cervical intraepithelial neoplasia; Human papillomavirus; Viral transcripts.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Capsid Proteins / genetics
  • Cervix Uteri / pathology
  • Cervix Uteri / virology
  • Female
  • Gene Expression Regulation, Viral*
  • Genotype*
  • Human papillomavirus 16 / genetics
  • Humans
  • Middle Aged
  • Oncogene Proteins, Viral / genetics
  • Papillomaviridae / classification
  • Papillomaviridae / genetics*
  • Uterine Cervical Dysplasia / virology*
  • Uterine Cervical Neoplasms / virology*

Substances

  • Capsid Proteins
  • Oncogene Proteins, Viral