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Androgen receptor molecular biology and potential targets in prostate cancer

机译:雄激素受体分子生物学和前列腺癌的潜在靶标

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The androgen receptor (AR) is a key transcriptional regulator and therapeutic target in prostate cancer. During androgen deprivation therapy to treat metastatic prostate cancer, surviving cells acquire increased AR signaling through a variety of mechanisms, one of which is enhanced interactions with AR coactivators. One recently identified AR-specific coregulator expressed only in human and nonhuman primates is the melanoma antigen gene protein-A11 (MAGE-11). MAGE-11 increases AR transcriptional activity through direct interactions with AR and other coactivators, and its levels increase during prostate cancer progression to castration-recurrent growth. The MAGE-11 gene is located at Xq28 on the human X chromosome as part of an X-linked MAGE gene family of cancer—testis antigens. MAGE-11 stabilizes AR when androgen levels are low, and functions in a transcriptional hub to promote AR-mediated gene activation. The evolutionary development and organization of the MAGE-11 gene within the cancer—testis antigen family suggests that MAGE-11 provides a gain-of-function to AR among primates in both normal physiology and cancer, and may serve as a therapeutic target in the treatment of advanced prostate cancer.
机译:雄激素受体(AR)是前列腺癌的关键转录调节因子和治疗靶标。在雄激素剥夺疗法治疗转移性前列腺癌的过程中,存活的细胞通过多种机制获得增强的AR信号传导,其中一种是增强与AR共激活因子的相互作用。最近发现的一种仅在人类和非人类灵长类动物中表达的AR特异性调节剂是黑色素瘤抗原基因蛋白A11(MAGE-11)。 MAGE-11通过与AR和其他共激活因子的直接相互作用来增加AR转录活性,并且在前列腺癌进展为去势复发的过程中,其水平升高。 MAGE-11基因位于人X染色体的Xq28处,是癌症的X连锁MAGE基因家族(睾丸抗原)的一部分。当雄激素水平低时,MAGE-11使AR稳定,并在转录中心起作用以促进AR介导的基因激活。癌–睾丸抗原家族中MAGE-11基因的进化发展和组织结构表明,MAGE-11在正常生理和癌症中都为灵长类提供AR的功能增强,并且可以作为癌症中的治疗靶标治疗晚期前列腺癌。

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