Detection and typing of human papillomavirus DNA in penile carcinoma - Evidence for multiple independent pathways of penile carcinogenesis

被引:311
作者
Rubin, MA
Kleter, B
Zhou, M
Ayala, G
Cubilla, AL
Quint, WGV
Pirog, EC
机构
[1] Cornell Univ, Weill Med Coll, Dept Pathol, New York, NY 10021 USA
[2] Univ Michigan, Dept Pathol, Ann Arbor, MI 48109 USA
[3] Delft Diagnost Lab, Delft, Netherlands
[4] Baylor Coll Med, Dept Pathol, Houston, TX 77030 USA
[5] Univ Nacl Asuncion, Dept Pathol, Asuncion, Paraguay
[6] Univ Amsterdam, Acad Med Ctr, NL-1105 AZ Amsterdam, Netherlands
关键词
D O I
10.1016/S0002-9440(10)62506-0
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
To clarify the role of human papillomavirus (HPV) in penile cancer we evaluated the prevalence of HPV DNA in different histological subtypes of penile carcinoma, dysplasia, and condyloma using a novel, sensitive SPF10 HPV polymerase chain reaction assay and a novel genotyping line probe assay, allowing simultaneous identification of 25 different HPV types. Formalin-fixed, paraffin-embedded tissue samples were collected from the United States and Paraguay. HPV DNA was detected in 42% cases of penile carcinoma, 90% cases of dysplasia, and 100% cases of condyloma. There were significant differences in HPV prevalence in different histological cancer subtypes. Although keratinizing squamous cell carcinoma and verrucous carcinoma were positive for HPV DNA in only 34.9 and 33.3% of cases, respectively, HPV DNA was detected in 80% of basaloid and 100% of warty tumor subtypes. There was no significant difference in BPV prevalence between cases from Paraguay and the United States. In conclusion, the overall prevalence of BPV DNA in penile carcinoma (42%) is lower than that in cervical carcinoma (similar to 100%) and similar to vulvar carcinoma (similar to 50%). In addition, specific histological subtypes of penile cancer-basaloid and warty - are consistently associated with HPV, however, only a subset of keratinizing and verrucous penile carcinomas is positive for BTV DNA, and thus these two tumor groups seem to develop along different pathogenetic pathways.
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页码:1211 / 1218
页数:8
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