首页> 外文期刊>The Journal of Steroid Biochemistry and Molecular Biology >Steroid receptor coactivators as therapeutic targets in the female reproductive system (Reprinted from J. Steroid Biochem. Mol. Biol., vol 154, pg 32-38, 2015)
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Steroid receptor coactivators as therapeutic targets in the female reproductive system (Reprinted from J. Steroid Biochem. Mol. Biol., vol 154, pg 32-38, 2015)

机译:类固醇受体共激活剂作为女性生殖系统中的治疗靶标(转载自《 J. Steroid Biochem。Mol。Biol。》,第154卷,第32-38页,2015年)

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摘要

The steroid receptor coactivators (SRCs/p160/NCOA) are a family of three transcriptional coregulators initially discovered to transactivate the transcriptional potency of steroid hormone receptors. Even though SRCs were also found to modulate the activity of multiple other transcription factors, their function is still strongly associated with regulation of steroid hormone action and many studies have found that they are critical for the regulation of reproductive biology. In the case of the female reproductive tract, SRCs have been found to play crucial roles in its physiology, ranging from ovulation, implantation, to parturition. Not surprisingly, SRCs' action has been linked to numerous abnormalities and debilitating disorders of female reproductive tissues, including infertility, cancer, and endometriosis. Many of these pathologies are still in critical need of therapeutic intervention and "proof-of-principle" studies have found that SRCs are excellent targets in pathological states. Therefore, small molecule modulators of SRCs' activity could be applied in the future in the treatment of many diseases of the female reproductive system. (C) 2015 Elsevier Ltd. All rights reserved.
机译:类固醇受体共激活因子(SRCs / p160 / NCOA)是最初发现可激活类固醇激素受体转录潜能的三个转录共调节因子家族。尽管还发现SRC可以调节多种其他转录因子的活性,但它们的功能仍然与类固醇激素作用的调节密切相关,许多研究发现它们对生殖生物学的调节至关重要。对于女性生殖道,已发现SRC在其生理中起着至关重要的作用,从排卵,着床到分娩。毫不奇怪,SRC的作用与女性生殖组织的许多异常和衰弱性疾病有关,包括不育,癌症和子宫内膜异位。这些病理中的许多仍然急需治疗干预,并且“原理验证”研究发现SRC在病理状态下是极好的靶标。因此,SRCs活性的小分子调节剂将来可用于治疗女性生殖系统的许多疾病。 (C)2015 Elsevier Ltd.保留所有权利。

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