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未折叠蛋白反应的预期性雌激素激活与雌激素受体α阳性乳腺癌的细胞增殖及不良预后相关。

Anticipatory estrogen activation of the unfolded protein response is linked to cell proliferation and poor survival in estrogen receptor α-positive breast cancer.

作者信息

Andruska N, Zheng X, Yang X, Helferich W G, Shapiro D J

机构信息

1] Department of Biochemistry, University of Illinois, Urbana, IL, USA [2] College of Medicine, University of Illinois, Urbana, IL, USA.

Department of Biochemistry, University of Illinois, Urbana, IL, USA.

出版信息

Oncogene. 2015 Jul;34(29):3760-9. doi: 10.1038/onc.2014.292. Epub 2014 Sep 29.

Abstract

In response to cell stress, cancer cells often activate the endoplasmic reticulum (EnR) stress sensor, the unfolded protein response (UPR). Little was known about the potential role in cancer of a different mode of UPR activation, anticipatory activation of the UPR prior to accumulation of unfolded protein or cell stress. We show that estrogen, acting via estrogen receptor α (ERα), induces rapid anticipatory activation of the UPR, resulting in increased production of the antiapoptotic chaperone BiP/GRP78, preparing cancer cells for the increased protein production required for subsequent estrogen-ERα-induced cell proliferation. In ERα-containing cancer cells, the estrogen, 17β-estradiol (E2) activates the UPR through a phospholipase C γ (PLCγ)-mediated opening of EnR IP3R calcium channels, enabling passage of calcium from the lumen of the EnR into the cytosol. siRNA knockdown of ERα blocked the estrogen-mediated increase in cytosol calcium and UPR activation. Knockdown or inhibition of PLCγ, or of IP3R, strongly inhibited the estrogen-mediated increases in cytosol calcium, UPR activation and cell proliferation. E2-ERα activates all three arms of the UPR in breast and ovarian cancer cells in culture and in a mouse xenograft. Knockdown of ATF6α, which regulates UPR chaperones, blocked estrogen induction of BiP and strongly inhibited E2-ERα-stimulated cell proliferation. Mild and transient UPR activation by estrogen promotes an adaptive UPR response that protects cells against subsequent UPR-mediated apoptosis. Analysis of data from ERα(+) breast cancers demonstrates elevated expression of a UPR gene signature that is a powerful new prognostic marker tightly correlated with subsequent resistance to tamoxifen therapy, reduced time to recurrence and poor survival. Thus, as an early component of the E2-ERα proliferation program, the mitogen estrogen, drives rapid anticipatory activation of the UPR. Anticipatory activation of the UPR is a new role for estrogens in cancer cell proliferation and resistance to therapy.

摘要

作为对细胞应激的反应,癌细胞常常激活内质网(EnR)应激传感器——未折叠蛋白反应(UPR)。对于UPR激活的另一种模式(即在未折叠蛋白积累或细胞应激之前对UPR进行预期激活)在癌症中的潜在作用,人们了解甚少。我们发现,雌激素通过雌激素受体α(ERα)发挥作用,可诱导UPR的快速预期激活,导致抗凋亡伴侣蛋白BiP/GRP78的产生增加,使癌细胞为随后雌激素-ERα诱导的细胞增殖所需的蛋白质产量增加做好准备。在含有ERα的癌细胞中,雌激素17β-雌二醇(E2)通过磷脂酶Cγ(PLCγ)介导的EnR IP3R钙通道开放来激活UPR,使钙从EnR腔进入细胞质。用小干扰RNA(siRNA)敲低ERα可阻断雌激素介导的细胞质钙增加和UPR激活。敲低或抑制PLCγ或IP3R,可强烈抑制雌激素介导的细胞质钙增加、UPR激活和细胞增殖。E2-ERα在培养的乳腺癌和卵巢癌细胞以及小鼠异种移植瘤中激活UPR的所有三个分支。调节UPR伴侣蛋白的ATF6α的敲低可阻断雌激素对BiP的诱导,并强烈抑制E2-ERα刺激的细胞增殖。雌激素引起的轻度和短暂的UPR激活促进了一种适应性UPR反应,可保护细胞免受随后UPR介导的凋亡。对ERα(+)乳腺癌数据的分析表明,一种UPR基因特征的表达升高,这是一种强大的新预后标志物,与随后对他莫昔芬治疗的耐药性、复发时间缩短和生存率低密切相关。因此,作为E2-ERα增殖程序的早期组成部分,有丝分裂原雌激素驱动UPR的快速预期激活。UPR的预期激活是雌激素在癌细胞增殖和治疗耐药性方面的一个新作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9df/4377305/832b5f136677/nihms618571f1.jpg

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