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SRC-3 has a role in cancer other than as a nuclear receptor coactivator

机译:SRC-3在癌症中的作用除了是核受体共激活剂以外

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摘要

Steroid receptor coactivator-3 (SRC-3), also known as AIB1, is a member of the p160 steroid receptor coactivator family. Since SRC-3 was found to be amplified in breast cancer in 1997, the role of SRC-3 in cancer has been broadly investigated. SRC-3 initially was identified as a transcriptional coactivator for nuclear receptors such as the estrogen receptor (ER), involved in the proliferation of hormone-dependent cancers. However, increasing clinical evidence shows that dysregulation of SRC-3 expression in several human hormone-independent cancers is correlated with pathological factors and clinical prognosis. Recently, both in vivo and in vitro studies demonstrate that SRC-3 may in-fluence a number of cancer cellular processes in several ways independent of nuclear receptor signaling. In addition, an SRC-3 transgenic mice model shows that SRC-3 in-duces tumors in several mouse tissues. These results indicate that the role of SRC-3 in cancer is not just as a nuclear receptor coactivator. The focus of this review is to examine possible SRC-3 roles in cancer, other than as a nuclear receptor coactivator.
机译:类固醇受体共激活因子3(SRC-3),也称为AIB1,是p160类固醇受体共激活因子家族的成员。自从SRC-3在1997年被发现在乳腺癌中被扩增以来,对SRC-3在癌症中的作用进行了广泛的研究。 SRC-3最初被确定为参与激素依赖性癌症增殖的核受体(如雌激素受体(ER))的转录共激活因子。然而,越来越多的临床证据表明,几种人类激素非依赖性癌症中SRC-3表达的失调与病理因素和临床预后相关。最近,体内和体外研究均表明SRC-3可能以几种独立于核受体信号传导的方式影响许多癌细胞的过程。此外,SRC-3转基因小鼠模型显示SRC-3可以在几种小鼠组织中诱发肿瘤。这些结果表明,SRC-3在癌症中的作用不仅是作为核受体共激活剂。这篇综述的重点是检查SRC-3在癌症中的可能作用,而不是作为核受体共激活剂。

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