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논문 기본 정보

자료유형
학술저널
저자정보
Zhang, Yu (Department of Urology, Shanghai Changning Center Hospital) Wang, Ji-Hong (Department of Urology, Shanghai Jiao Tong University Affiliated 6th People's Hospital) Liu, Bin (Shanghai Institute of Materia Medica Chinese Academy of Sciences) Qu, Ping-Bao (Department of Urology, Shanghai Changning Center Hospital)
저널정보
아시아태평양암예방학회 Asian Pacific journal of cancer prevention : APJCP Asian Pacific journal of cancer prevention : APJCP 제14권 제6호
발행연도
2013.1
수록면
3,847 - 3,850 (4page)

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The three homologous members of the p160 SRC family (SRC-1, SRC-2 and SRC-3) mediate the transcriptional functions of nuclear receptors and other transcription factors, and are the most studied of all the transcriptional co-activators. Recent work has indicated that the SRC-3 gene is subject to amplification and overexpression in various human cancers. Some of the molecular mechanisms responsible for SRC overexpression, along with the mechanisms by which SRC-3 promotes breast and prostate cancer cell proliferation and survival, have been identified. However, the function of SRC-3 in bladder cancer remains poorly understood. In the present study, our results indicate that overexpression of SRC-3 promotes bladder cancer cell proliferation whereas knockdown of SRC-3 results in inhibition. At the molecular level, we further established that CXCR4 is a transcriptional target of SRC-3. Therefore, our study first identified that SRC-3 plays a critical role in the bladder cancer, which may be a target beneficial for its prevention and treatment.

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