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    Please use this identifier to cite or link to this item: https://ir.csmu.edu.tw:8080/ir/handle/310902500/11043


    Title: The high incidence of JC virus infection in urothelial carcinoma tissue in Taiwan
    Authors: Shen, Cheng-Huang
    Wu, Jiann-Der
    Hsu, Cheng-Da
    Jou, Yeong-Chin
    Lin, Chang-Te
    Wang, Meilin
    Wu, Shu-Fen
    Michael, W.Y.Chan
    Chiang, Ming-Ko
    Fang, Chiung-Yao
    Chang, Deching
    Contributors: 中山醫學大學
    Keywords: human polyomavirus infection;carcinogenesis;nested PCR
    Date: 2011
    Issue Date: 2015-07-03T05:32:32Z (UTC)
    ISSN: 0146-6615
    Abstract: Human polyomaviruses, JC virus (JCV) and BK virus (BKV), usually remain latent in kidney and urothelial tissue after primary infection. Infection with human polyomavirus has still not been correlated conclusively with malignancy of kidney and urothelial tissue. The present study investigated further the possible relationship between JCV/BKV infection and urothelial carcinoma. Tissue samples were examined from 33 urothelial carcinomas and 5 renal cell carcinomas for JCV/BKV infection, using nested PCR with primers common to both JCV and BKV. The viral genotypes were further verified by endonuclease digestion and DNA sequencing following the PCR. In addition, immunohistochemistry and Western blotting were also performed to detect viral large tumor protein (LT) and the late capsid protein (VP1) in the tissue samples. The results from nested PCR showed that 90.1% (30/33) of the urothelial carcinomas samples and all of the renal cell carcinomas samples (5/5) were JCV DNA positive. Both archetypal and re-arranged JCV genotypes were detected. On the other hand, BKV DNA was detected in only one (3%) of the urothelial carcinoma tissue samples. The immunohistochemical results showed that 30% (10/33) of urothelial carcinoma tissues was stained positive for large tumor antigen (LT). However, the structural protein VP1 was not detectable in any of the tissue samples examined. The present study demonstrated that JCV is highly prevalent in urothelial carcinoma tissue as is the expression of large tumor antigen. Therefore, the findings support the hypothesis that JCV infection is associated with urothelial carcinoma. J. Med. Virol. 83:2191–2199, 2011. © 2011 Wiley Periodicals, Inc.
    URI: https://ir.csmu.edu.tw:8080/ir/handle/310902500/11043
    http://dx.doi.org/10.1002/jmv.22240
    Relation: Journal of Medical Virology Volume 83, Issue 12, pages 2191–2199, December 2011
    Appears in Collections:[生化微生物免疫研究所] 期刊論文

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