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
. 2006 Jun 19;94(12):1913-7.
doi: 10.1038/sj.bjc.6603179. Epub 2006 May 30.

Detection of adeno-associated virus type 2 genome in cervical carcinoma

Affiliations

Detection of adeno-associated virus type 2 genome in cervical carcinoma

B Y Zheng et al. Br J Cancer. .

Abstract

Adeno-associated virus (AAV) can impair the replication of other viruses. Adeno-associated virus seroprevalences have been reported to be lower among women with cervical cancer. In-vitro, AAV can interfere with the production of human papillomavirus virions. Adeno-associated virus-2 DNA has also been detected in cervical cancer tissue, although not consistently. To evaluate the role of AAV infection in relation to invasive cervical cancer, we performed a nested case-control study within a retrospectively followed population-based cohort. A total of 104 women who developed invasive cervical cancer on average 5.6 years of follow-up (range: 0.5 months-26.2 years) and 104 matched control-women who did not develop cervical cancer during the same follow-up time were tested for AAV and human papillomavirus by polymerase chain reaction. At baseline, two (2%) case-women and three (3%) control-women were positive for AAV-2 DNA. At the time of cancer diagnosis, 12 (12%) case-women and 3 (3%) matched control-women were positive for AAV-2 DNA. Persisting AAV infection was not evident. In conclusion, AAV-2 DNA was present in a low proportion of cervical cancers and we found no evidence that the presence of AAV in cervical smears of healthy women would be associated with reduced risk of cervical cancer.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Agrawal N, Mane M, Chiriva-Internati M, Roman JJ, Hermonat PL (2002) Temporal acceleration of the human papillomavirus life cycle by adeno-associated virus (AAV) type 2 superinfection in natural host tissue. Virology 297: 203–210 - PubMed
    1. Ahn WS, Bae SM, Chung JE, Lee HK, Kim BK, Lee JM, Namkoong SE, Kim CK, Sin J (2003) Evaluation of adenoassociated virus 2 and human papilloma virus 16 and 18 infection in cervical cancer biopsies. Gynecol Oncol 89: 105–111 - PubMed
    1. Ahn WS, Bae SM, Lee HJ, Kim YW, Lee JM, Namkoong SE, Kim CK, Jin HS (2006) Development of anticancer gene vaccine interact with human papillomavirus oncoprotein inhibition. Int J Gynecol Cancer 16: 270–276 - PubMed
    1. Alazawi W, Pett M, Arch B, Scott L, Freeman T, Stanley MA, Coleman N (2002) Changes in cervical keratinocyte gene expression associated with integration of human papillomavirus 16. Cancer Res 62: 6959–6965 - PubMed
    1. Atchison RW, Casto BC, Hammon WM (1965) Adenovirus-associated defective virus particles. Science 149: 754–756 - PubMed

Publication types