Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2003 Jan;16(1):1-17.
doi: 10.1128/CMR.16.1.1-17.2003.

Human papillomavirus and cervical cancer

Affiliations
Review

Human papillomavirus and cervical cancer

Eileen M Burd. Clin Microbiol Rev. 2003 Jan.

Abstract

Of the many types of human papillomavirus (HPV), more than 30 infect the genital tract. The association between certain oncogenic (high-risk) strains of HPV and cervical cancer is well established. Although HPV is essential to the transformation of cervical epithelial cells, it is not sufficient, and a variety of cofactors and molecular events influence whether cervical cancer will develop. Early detection and treatment of precancerous lesions can prevent progression to cervical cancer. Identification of precancerous lesions has been primarily by cytologic screening of cervical cells. Cellular abnormalities, however, may be missed or may not be sufficiently distinct, and a portion of patients with borderline or mildly dyskaryotic cytomorphology will have higher-grade disease identified by subsequent colposcopy and biopsy. Sensitive and specific molecular techniques that detect HPV DNA and distinguish high-risk HPV types from low-risk HPV types have been introduced as an adjunct to cytology. Earlier detection of high-risk HPV types may improve triage, treatment, and follow-up in infected patients. Currently, the clearest role for HPV DNA testing is to improve diagnostic accuracy and limit unnecessary colposcopy in patients with borderline or mildly abnormal cytologic test results.

PubMed Disclaimer

Figures

FIG. 1.
FIG. 1.
Schematic representation of the circular HPV DNA genome.
FIG. 2.
FIG. 2.
Pathogenesis of oncogenic HPV. HPV E6 and E7 genes encode multifunctional proteins that bind primarily to cellular p53 and pRB proteins, disrupt their functions, and alter cell cycle regulatory pathways, leading to cellular transformation.
FIG. 3.
FIG. 3.
Cervical condyloma showing proliferation of the suprabasal epithelial layers and koilocytic atypia, consisting of nuclear pyknosis and a well-defined perinuclear cavity associated with peripherally thickened cytoplasm. Reprinted with permission of S. Kini.
FIG. 4.
FIG. 4.
ThinPrep Pap Smear showing abnormal squamous cells with HPV cytopathic effect (arrow), consistent with LSIL.

References

    1. Adam, E., Z. Berkova, Z. Daxnerova, J. Icenogle, W. C. Reeves, and R. H. Kaufman. 2000. Papillomavirus detection: demographic and behavioral characteristics influencing the identification of cervical disease. Am. J. Obstet. Gynecol. 182:257-264. - PubMed
    1. Allen, M., M. Kalantari, N. Ylitalo, B. Pettersson, B. Hagmar, L. Scheibenplug, B. Johansson, U. Petterson, and U. Gyllensten. 1996. HLA DQ-DR haplotype and susceptibility to cervical carcinoma: indications of increased risk for development of cervical carcinoma in individuals infected with HPV 18. Tissue Antigens 48:32-37. - PubMed
    1. Andersson, S., E. Rylander, B. Larsson, A. Strand, C. Silfversvard, and E. Wilander. 2001. The role of human papillomavirus in cervical adenocarcinoma carcinogenesis. Eur. J. Cancer 37:246-250. - PubMed
    1. Andrei, G., R. Snoeck, J. Piette, P. Delvenne, and E. DeClercq. 1998. Antiproliferative effects of acyclic nucleoside phosphonates on human papillomavirus (HPV)-harboring cell lines compared with HPV-negative cell lines. Oncol. Res. 10:523-531. - PubMed
    1. Apple R. J., T. M. Becker, C. M. Wheeler, and H. A. Erlich. 1995. Comparison of human leukocyte antigen DR-DQ disease associations found with cervical dysplasia and invasive cervical carcinoma. J. Natl. Cancer Inst. 87:427-436. - PubMed

MeSH terms