DETECTION OF HUMAN PAPILLOMAVIRUS (HPV) DNA IN HUMAN PROSTATIC TISSUES BY POLYMERASE CHAIN-REACTION (PCR)

被引:39
|
作者
SARKAR, FH
SAKR, WA
LI, YW
SREEPATHI, P
CRISSMAN, JD
机构
[1] Department of Pathology, Wayne State University School of Medicine and Harper Hospital, Detroit, Michigan
来源
PROSTATE | 1993年 / 22卷 / 02期
关键词
PROSTATE CANCER; DNA VIRUS; SOUTHERN HYBRIDIZATION; CHEMILUMINESCENT DETECTION;
D O I
10.1002/pros.2990220210
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Human papillomavirus (HPV) infections are strongly linked to the pathogenesis of uterine cervical neoplasms, and have been implicated in other cancers of the female genital tract. In contrast, the association of HPV with the cancers of the male urogenital tract is less evident, except in anal and penile cancers. However, recent studies reporting the prevalence of HPV infections in human prostate cancers (60-100% HPV 16 positive vs. no infection of HPV) have raised controversies regarding the prevalence of HPV in benign and neoplastic human prostate. We investigated the prevalence of HPV infections in prostatic intraepithelial neoplasia (PIN) and prostatic adenocarcinomas in 23 surgically resected prostates. Polymerase chain reaction (PCR) was used to amplify HPV 6b/11, 16, and 18 specific DNA sequences, using type specific HPV primers selected from the transforming gene E6-E7. The areas of PIN and cancer in 6 mum H&E stained tissue sections were identified, and respective areas of PIN and cancer were isolated from the adjacent serial sections and used for DNA amplification and HPV detection (Fig. 1). Our results demonstrated the presence of HPV 16 in three carcinomas (13%), using type specific primers in PCR amplified samples. We were not able to demonstrate the presence of other HPV types (HPV 6b/11 or HPV 18) in any of the samples using specific primers. Two of these prostates showed relatively strong positive signals by dot blot analysis, when hybridized with a P-32-labeled HPV 16 type specific oligonucleotide probe. One more sample showed weak positivity, when hybridized with a P-32-labeled HPV 16 type specific oligonucleotide probe. Subsequently, we have confirmed these results by Southern hybridization of the samples transferred to nylon membrane after agarose gel electrophoresis and detected by HPV 16 type specific oligonucleotide probe, using chemiluminescent assay. We, therefore, conclude that HPV infections of the prostate in general are not as common as has been previously claimed by other investigators.
引用
收藏
页码:171 / 180
页数:10
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