雌激素受体α的P295-T311基序的调控功能——受体的蛋白酶体降解是否会诱导与雌激素反应有关的肽的出现?

Dominique Gallo, Iman Haddad, Guy Laurent, Joëlle Vinh, Françoise Jacquemotte, Yves Jacquot, Guy Leclercq
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引用次数: 12

摘要

雌激素受体α (er - α)介导基因转录和激素依赖性癌细胞增殖的方式,在最近的几项发现中得到了很大程度上的重新考虑。erα介导的转录似乎是一个循环和短暂的过程,其中蛋白酶体-因此受体降解-起关键作用。鉴于我们最近的研究表明,与受体的调节基序(ERalpha17p)相对应的合成肽具有雌激素活性,我们提出ERalpha蛋白酶体降解可能诱导调节肽的出现。后者将作为一个信号,促进erα激活过程,放大最初的激素刺激,并引起持续的雌激素反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Regulatory function of the P295-T311 motif of the estrogen receptor alpha - does proteasomal degradation of the receptor induce emergence of peptides implicated in estrogenic responses?

Regulatory function of the P295-T311 motif of the estrogen receptor alpha - does proteasomal degradation of the receptor induce emergence of peptides implicated in estrogenic responses?

Regulatory function of the P295-T311 motif of the estrogen receptor alpha - does proteasomal degradation of the receptor induce emergence of peptides implicated in estrogenic responses?

Regulatory function of the P295-T311 motif of the estrogen receptor alpha - does proteasomal degradation of the receptor induce emergence of peptides implicated in estrogenic responses?

The way in which estrogen receptor alpha (ERalpha) mediates gene transcription and hormone-dependent cancer cell proliferation is now being largely reconsidered in view of several recent discoveries. ERalpha-mediated transcription appears to be a cyclic and transient process where the proteasome - and thus receptor degradation - plays a pivotal role. In view of our recent investigations, which demonstrate the estrogenic activity of a synthetic peptide corresponding to a regulatory motif of the receptor (ERalpha17p), we propose that ERalpha proteasomal degradation could induce the emergence of regulatory peptide(s). The latter would function as a signal and contribute to the ERalpha activation process, amplifying the initial hormonal stimulation and giving rise to sustained estrogenic response.

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