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September 1, 1999The Journal of Pathology9,101 citationsOpen Access

Human papillomavirus is a necessary cause of invasive cervical cancer worldwide

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JWJan M.M. WalboomersMJMarcel V. JacobsMMM. Michele Manos

Key Points

  • To re-evaluate formerly HPV-negative invasive cervical cancer specimens using advanced serological and PCR assays to determine the true worldwide prevalence of HPV in cervical cancer.
  • Tested serum antibodies to HPV 16 VLPs, E6, and E7 in 49 originally HPV-negative and 48 HPV-positive cases.
  • Reanalyzed 55 of 66 formerly HPV-negative biopsies using a sandwich histological and multi-target PCR protocol covering type-specific E7 (14 high-risk types), E1, and L1 open reading frames.
  • HPV DNA was detected in 40 of 55 (73%) reanalyzed specimens via type-specific E7 PCR (38 cases) and E1/L1 consensus PCR (2 cases), identifying HPV types 16, 18, 31, 33, 39, 45, 52, and 58.
  • Histological assessment showed 21 of 55 samples were inadequate; among 34 adequate samples, only 2 were HPV-negative across all PCR assays compared to 13 of 21 inadequate samples (p < 0.001).
  • Adjusting for specimen adequacy and pooling data yielded a worldwide HPV prevalence of 99.7% in invasive cervical cancer.

Abstract

A recent report that 93 per cent of invasive cervical cancers worldwide contain human papillomavirus (HPV) may be an underestimate, due to sample inadequacy or integration events affecting the HPV L1 gene, which is the target of the polymerase chain reaction (PCR)-based test which was used. The formerly HPV-negative cases from this study have therefore been reanalyzed for HPV serum antibodies and HPV DNA. Serology for HPV 16 VLPs, E6, and E7 antibodies was performed on 49 of the 66 cases which were HPV-negative and a sample of 48 of the 866 cases which were HPV-positive in the original study. Moreover, 55 of the 66 formerly HPV-negative biopsies were also reanalyzed by a sandwich procedure in which the outer sections in a series of sections are used for histological review, while the inner sections are assayed by three different HPV PCR assays targeting different open reading frames (ORFs). No significant difference was found in serology for HPV 16 proteins between the cases that were originally HPV PCR-negative and -positive. Type-specific E7 PCR for 14 high-risk HPV types detected HPV DNA in 38 (69 per cent) of the 55 originally HPV-negative and amplifiable specimens. The HPV types detected were 16, 18, 31, 33, 39, 45, 52, and 58. Two (4 per cent) additional cases were only HPV DNA-positive by E1 and/or L1 consensus PCR. Histological analysis of the 55 specimens revealed that 21 were qualitatively inadequate. Only two of the 34 adequate samples were HPV-negative on all PCR tests, as against 13 of the 21 that were inadequate ( p< 0.001). Combining the data from this and the previous study and excluding inadequate specimens, the worldwide HPV prevalence in cervical carcinomas is 99.7 per cent. The presence of HPV in virtually all cervical cancers implies the highest worldwide attributable fraction so far reported for a specific cause of any major human cancer. The extreme rarity of HPV-negative cancers reinforces the rationale for HPV testing in addition to, or even instead of, cervical cytology in routine cervical screening.

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Cite This Study

Walboomers et al. (1999) studied this question.

synapsesocial.com/papers/69d848e5d2f7327e70ae2990https://doi.org/10.1002/(sici)1096-9896(199909)189:1<12::aid-path431>3.0.co;2-f
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