AI Article Synopsis

  • The study investigates the expression of the protein PIWIL2 in human bladder cancer and finds that it is mainly expressed in testis tissue but not in bladder tissues or cancer cell lines.
  • Researchers used quantitative RT-PCR to compare PIWIL2 expression across various bladder carcinoma cell lines and tissue samples, revealing that it was significantly lower in these compared to testis.
  • While PIWIL2 shows potential as a tumor marker, the findings suggest it does not contribute to the development of human bladder cancer.

Article Abstract

Background: PIWIL2, a member of Argonaute family of proteins, is exclusively expressed in testis and functions in development and maintenance of germline stem cells. Recently, ectopic expression of PIWIL2 has been reported in a variety of human and mouse tumors. To investigate a potential involvement of PIWIL2 in human bladder cancer, we examined its expression in several human bladder cancer cell lines, normal uroepithelial cell cultures, and some bladder tissues.

Methods: Relative expression of PIWIL2 was determined by real-time quantitative RT-PCR in fifteen bladder carcinoma cell lines, six normal uroepithelial cell cultures and seventy tissue specimens of tumor, tumor margins and morphologically normal tissues of bladder. Specific primers for PIWIL2, TBP and GAPDH (as two internal controls) were used for reverse transcription polymerase chain reaction technique.

Results: Real-time qRT-PCR demonstrated high PIWIL2 expression in testis tissue, but at least 240-fold lower expression in all examined cell lines. The highest expression outside testis was observed in one of six primary cultures of normal uroepithelial cells, but even lower expression of PIWIL2 was detected in any of the examined tumor and non-tumor tissues.

Conclusion: Lack of PIWIL2 expression in most tissues along with its aberrant expression in some tumors candidate the gene as an attractive tumor marker for some neoplasms. However, our study indicates that PIWIL2 does not play a role in carcinogenesis of human bladder carcinoma.

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Source
http://dx.doi.org/10.1016/j.canep.2009.06.011DOI Listing

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