Etiological role of human papillomavirus infection in the development of penile cancer

Int J Infect Dis. 2019 Jan:78:148-154. doi: 10.1016/j.ijid.2018.11.003. Epub 2018 Nov 10.

Abstract

Objective: To examine the association between human papillomavirus (HPV) infection and penile cancer among Japanese patients.

Methods: Thirty-four patients with penile cancer were enrolled in this study. DNA was extracted from paraffin-embedded tumor tissue samples, and HPV-DNA tests and genotyping were performed. For all of the samples, in situ hybridization (ISH) was performed to locate HPV-DNA in tumor tissue. Furthermore, expression levels of p16-INK4a, mini-chromosome maintenance protein 7(mcm-7), HPV-L1, and Ki-67 were analyzed using immunohistochemical methods.

Results: HPV and high-risk (HR)-HPV were detected in 14 (41.1%; 95% confidence interval (CI) 24.6-57.7%) and 12 (35.2%; 95% CI 19.2-51.4%) cases, respectively. HPV16 was the most frequently detected HPV type. Among the HR-HPV-positive cases, a punctate HR-HPV-DNA signal pattern was detected by ISH in tumor cell nuclei. P16-INK4a was expressed in 66.7% (95% CI 42.8-90.1%) of HR-HPV-positive cases and was significantly more frequent and stronger in HR-HPV-positive cases than in HPV-negative cases. There was no significant difference in the occurrence or distribution of mcm-7 or Ki-67 expression between HPV-positive and HPV-negative cases. HPV-L1 expression was not observed in any of the cases examined.

Conclusions: HPV infection may have had an etiological role in 41% of the examined cases of penile cancer in Japan.

Keywords: Human papillomavirus; Ki-67; Mini-chromosome maintenance protein 7; Penile cancer; p16-INK4a.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Cyclin-Dependent Kinase Inhibitor p16 / analysis
  • Female
  • Humans
  • Ki-67 Antigen / analysis
  • Male
  • Middle Aged
  • Minichromosome Maintenance Complex Component 7 / analysis
  • Papillomavirus Infections / complications*
  • Penile Neoplasms / chemistry
  • Penile Neoplasms / etiology*

Substances

  • CDKN2A protein, human
  • Cyclin-Dependent Kinase Inhibitor p16
  • Ki-67 Antigen
  • MCM7 protein, human
  • Minichromosome Maintenance Complex Component 7