Detection of human papillomavirus DNA in malignant lesions from Chinese women with carcinomas of the upper genital tract

Gynecol Oncol. 2002 Oct;87(1):104-11. doi: 10.1006/gyno.2002.6784.

Abstract

Objective: The aim of this study was to determine the prevalence of high-risk oncogenic human papillomaviruses (HPVs) in malignant lesions from Hong Kong Chinese women with carcinomas of the upper genital tract.

Methods: The presence of high-risk HPVs in 55 cases of endometrial adenocarcinomas and 60 cases of primary epithelial ovarian cancers was detected by polymerase chain reaction (PCR) using consensus primers complementary to late 1 (L1) gene of the genital HPVs. Amplified PCR products were verified and typed by Southern blot analysis using (32)P-labeled DNA probes prepared from cloned HPV-16 and -18 plasmids. To confirm the presence of high-risk HPV types in the tumor tissues, PCR amplification using HPV type 16- and 18-specific primers for part of the E6 gene were also carried out.

Results: While HPV-18 was not detected, HPV-16 DNA sequences were identified in 5 (9.1%) of the 55 studied endometrial carcinoma samples. Of the 5 HPV-16-positive cases, there were 4 stage I, and 1 stage II endometrial cancer. In addition, 6 (10%) of the 60 epithelial ovarian carcinomas were positive for high-risk HPVs, which included 5 cases with HPV-16 and 1 case with HPV-18. Clinical staging revealed that 5 of the 6 HPV-positive cases were stage I and the remaining case was stage III ovarian cancer. Histology of the 6 HPV-positive cases showed that there were 1 case of clear-cell adenocarcinoma, 1 case of mucinous cystadenocarcinoma, and 4 cases of mucinous tumor of borderline malignancy. No other HPV types were detected.

Conclusion: High-risk HPV was detected in approximately 10% of the tumor samples from women with upper genital tract carcinomas. As compared to the high positive rate of HPV infections in cervical cancer, it appears that HPV infection plays a relatively minor role in the pathogenesis of endometrial and ovarian carcinomas.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma / virology*
  • Adult
  • Aged
  • Aged, 80 and over
  • Capsid Proteins*
  • Consensus Sequence
  • DNA Primers
  • DNA, Viral / analysis*
  • DNA, Viral / genetics
  • DNA-Binding Proteins*
  • Endometrial Neoplasms / virology*
  • Female
  • Humans
  • Middle Aged
  • Oncogene Proteins, Viral / genetics
  • Ovarian Neoplasms / virology*
  • Papillomaviridae / genetics*
  • Papillomavirus Infections / complications
  • Papillomavirus Infections / virology
  • Polymerase Chain Reaction
  • Repressor Proteins*
  • Tumor Virus Infections / complications
  • Tumor Virus Infections / virology

Substances

  • Capsid Proteins
  • DNA Primers
  • DNA, Viral
  • DNA-Binding Proteins
  • E6 protein, Human papillomavirus type 16
  • E6 protein, Human papillomavirus type 18
  • Oncogene Proteins, Viral
  • Repressor Proteins
  • L1 protein, Human papillomavirus type 16