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高尔基体膜蛋白TMEM165在控制乳腺癌迁移和侵袭中的新作用。

Novel role for the Golgi membrane protein TMEM165 in control of migration and invasion for breast carcinoma.

作者信息

Murali Pavitra, Johnson Blake P, Lu Zhongpeng, Climer Leslie, Scott Danielle A, Foulquier Francois, Oprea-Ilies Gabriela, Lupashin Vladimir, Drake Richard R, Abbott Karen L

机构信息

University of Oklahoma Health Sciences Center, Department of Biochemistry and Molecular Biology, Oklahoma City, OK, United States.

Ouchita Baptist University, Department of Biology, Arkadelphia, AR, United States.

出版信息

Oncotarget. 2020 Jul 14;11(28):2747-2762. doi: 10.18632/oncotarget.27668.

Abstract

The gene encodes for a multiple pass membrane protein localized in the Golgi that has been linked to congenital disorders of glycosylation. The TMEM165 protein is a putative ion transporter that regulates H/Ca/Mn homeostasis and pH in the Golgi. Previously, we identified TMEM165 as a potential biomarker for breast carcinoma in a glycoproteomic study using late stage invasive ductal carcinoma tissues with patient- matched adjacent normal tissues. The TMEM165 protein was not detected in non-malignant matched breast tissues and was detected in invasive ductal breast carcinoma tissues by mass spectrometry. Our hypothesis is that the TMEM165 protein confers a growth advantage to breast cancer. In this preliminary study we have investigated the expression of TMEM165 in earlier stage invasive ductal carcinoma and ductal carcinoma cases. We created a CRISPR/Cas9 knockout of TMEM165 in the human invasive breast cancer cell line MDAMB231. Our results indicate that removal of TMEM165 in these cells results in a significant reduction of cell migration, tumor growth, and tumor vascularization . Furthermore, we find that TMEM165 expression alters the glycosylation of breast cancer cells and these changes promote the invasion and growth of breast cancer by altering the expression levels of key glycoproteins involved in regulation of the epithelial to mesenchymal transition such as E-cadherin. These studies illustrate new potential functions for this Golgi membrane protein in the control of breast cancer growth and invasion.

摘要

该基因编码一种定位于高尔基体的多次跨膜蛋白,它与先天性糖基化障碍有关。TMEM165蛋白是一种推测的离子转运蛋白,可调节高尔基体中的H/Ca/Mn稳态和pH值。此前,在一项糖蛋白质组学研究中,我们使用晚期浸润性导管癌组织及其配对的癌旁正常组织,将TMEM165鉴定为乳腺癌的潜在生物标志物。在配对的非恶性乳腺组织中未检测到TMEM165蛋白,而通过质谱分析在浸润性导管癌组织中检测到了该蛋白。我们的假设是,TMEM165蛋白赋予乳腺癌生长优势。在这项初步研究中,我们调查了TMEM165在早期浸润性导管癌和导管原位癌病例中的表达情况。我们在人浸润性乳腺癌细胞系MDAMB231中创建了TMEM165的CRISPR/Cas9基因敲除模型。我们的结果表明,去除这些细胞中的TMEM165会导致细胞迁移、肿瘤生长和肿瘤血管生成显著减少。此外,我们发现TMEM165的表达改变了乳腺癌细胞的糖基化,并且这些变化通过改变参与上皮-间质转化调控的关键糖蛋白(如E-钙黏蛋白)的表达水平来促进乳腺癌的侵袭和生长。这些研究揭示了这种高尔基体膜蛋白在控制乳腺癌生长和侵袭方面的新潜在功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d00f/7367651/afbaecb75044/oncotarget-11-2747-g001.jpg

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