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TGFα-EGFR 通路在乳腺癌发生中的作用,与 WWOX 表达和雌激素激活的关联。

TGFα-EGFR pathway in breast carcinogenesis, association with WWOX expression and estrogen activation.

机构信息

Department of Molecular Carcinogenesis, Medical University of Lodz, Lodz, Poland.

出版信息

J Appl Genet. 2022 May;63(2):339-359. doi: 10.1007/s13353-022-00690-3. Epub 2022 Mar 15.

Abstract

WWOX is a tumor-suppressive steroid dehydrogenase, which relationship with hormone receptors was shown both in animal models and breast cancer patients. Herein, through nAnT-iCAGE high-throughput gene expression profiling, we studied the interplay of estrogen receptors and the WWOX in breast cancer cell lines (MCF7, T47D, MDA-MB-231, BT20) under estrogen stimulation and either introduction of the WWOX gene by retroviral transfection (MDA-MB-231, T47D) or silenced with shRNA (MCF7, BT20). Additionally, we evaluated the consequent biological characteristics by proliferation, apoptosis, invasion, and adhesion assays. TGFα-EGFR signaling was found to be significantly affected in all examined breast cancer cell lines in response to estrogen and strongly associated with the level of WWOX expression, especially in ER-positive MCF7 cells. Under the influence of 17β-estradiol presence, biological characteristics of the cell lines were also delineated. The study revealed modulation of adhesion, invasion, and apoptosis. The obtained results point at a complex role of the WWOX gene in the carcinogenesis of the breast tissue, which seems to be closely related to the presence of estrogen α and/or β receptors.

摘要

WWOX 是一种肿瘤抑制性甾体脱氢酶,其与激素受体的关系在动物模型和乳腺癌患者中均有显示。在此,通过 nAnT-iCAGE 高通量基因表达谱分析,我们研究了雌激素刺激下乳腺癌细胞系(MCF7、T47D、MDA-MB-231、BT20)中雌激素受体和 WWOX 之间的相互作用,以及通过逆转录病毒转染引入 WWOX 基因(MDA-MB-231、T47D)或用 shRNA 沉默(MCF7、BT20)的情况。此外,我们还通过增殖、凋亡、侵袭和黏附测定评估了随后的生物学特性。发现 TGFα-EGFR 信号在所有检测到的乳腺癌细胞系中均受到雌激素的显著影响,并且与 WWOX 表达水平强烈相关,特别是在 ER 阳性 MCF7 细胞中。在 17β-雌二醇存在的影响下,细胞系的生物学特性也得到了描绘。研究揭示了黏附、侵袭和凋亡的调节。所得结果表明 WWOX 基因在乳腺组织癌变中起着复杂的作用,这似乎与雌激素 α 和/或 β 受体的存在密切相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7649/8979909/94d160698f00/13353_2022_690_Fig1_HTML.jpg

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