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中国临床药理学与治疗学 ›› 2020, Vol. 25 ›› Issue (7): 791-795.doi: 10.12092/j.issn.1009-2501.2020.07.011

• 综述与讲座 • 上一篇    下一篇

前列腺癌细胞内TMPRSS2-ERG融合基因产物转录调控机制研究进展

曹颖,屠凌岚,王孝举,郑晓亮   

  1. 浙江省医学科学院分子医学中心,杭州 310013,浙江
  • 收稿日期:2020-03-12 修回日期:2020-06-04 出版日期:2020-07-26 发布日期:2020-07-31
  • 通讯作者: 郑晓亮,通信作者,男,副研究员,硕士生导师,研究方向:抗肿瘤药物研究。 Tel: 0571-88215563 E-mail: zhengxl@zjams.com.cn
  • 作者简介:曹颖,女,硕士研究生,研究方向:抗肿瘤药物研究。
  • 基金资助:
    国家自然科学基金(81773626);浙江省院所专项(CF1923D-04)

Progress on TMPRSS2-ERG fusion gene product transcription regulation mechanism in prostate cancer cells

CAO Ying, TU Linglan, WANG Xiaoju, ZHENG Xiaoliang   

  1. Center for Molecular Medicine, Zhejiang Academy of Medical Sciences, Hangzhou 310013, Zhejiang, China
  • Received:2020-03-12 Revised:2020-06-04 Online:2020-07-26 Published:2020-07-31

摘要: 前列腺癌在欧美国家男性中是最常见的恶性肿瘤,但前列腺癌的发生发展机制还未完全明确。在前列腺癌中,TMPRSS2-ERG融合基因具有较高的发生率,其促进ERG过表达,引起相应的靶基因和信号通路改变,如雄激素受体、斑点型锌指结构蛋白、Notch通路等。深入了解前列腺癌细胞中TMPRSS2-ERG融合基因产物转录调控机制,可以为前列腺癌的治疗提供新的药物作用靶点。

关键词: 前列腺癌, TMPRSS2-ERG融合基因, 雄激素受体, 斑点型锌指结构蛋白, Notch通路

Abstract: Prostate cancer is the most common malignant tumor in men in Europe and the United States, but the mechanism of prostate cancer occurrence and development is not completely clear. In prostate cancer, the TMPRSS2-ERG fusion gene has a high incidence, which promotes ERG overexpression and causes changes in target genes and signaling pathways, such as androgen receptors, spotted zinc finger structural proteins, Notch pathways. In-depth understanding of the transcriptional regulation mechanism of TMPRSS2-ERG fusion gene products in prostate cancer cells can provide new targets for drug action in the treatment of prostate cancer.

Key words: prostate cancer, TMPRSS2-ERG fusion gene, androgen receptors, spotted zinc finger structural proteins, Notch pathways

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