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二甲双胍可诱导乳腺癌细胞中mTOR蛋白的降解。

Metformin induces degradation of mTOR protein in breast cancer cells.

作者信息

Alalem Mohamed, Ray Alpana, Ray Bimal K

机构信息

Department of Veterinary Pathobiology, University of Missouri, Columbia, Missouri, 65211.

出版信息

Cancer Med. 2016 Nov;5(11):3194-3204. doi: 10.1002/cam4.896. Epub 2016 Oct 17.

Abstract

Activation of mTOR is implicated in the development and progression of breast cancer. mTOR inhibition exhibited promising antitumor effects in breast cancer; however, its effect is compromised by several feedback mechanisms. One of such mechanisms is the upregulation of mTOR pathway in breast cancer cells. Despite the established role of mTOR activation in breast cancer, the status of total mTOR protein and its impact on the tumor behavior and response to treatment are poorly understood. Besides, the mechanisms underlying mTOR protein degradation in normal and cancer breast cells are still largely unknown. We and others found that total mTOR protein level is elevated in breast cancer cells compared to their nonmalignant counterparts. We have detected defective proteolysis of mTOR protein in breast cancer cells, which could, at least in part, explain the high level of mTOR protein in these cells. We show that metformin treatment in MCF-7 breast cancer cells induced degradation of mTOR and sequestration of this protein in a perinuclear region. The decrease in mTOR protein level in these cells correlated positively with a concomitant inhibition of proliferation and migration potentials of these cells. These findings provided a novel mechanism for the metformin action in breast cancer treatment. Understanding the proteolytic mechanism responsible for mTOR level in breast cancer may pave the way for improving the efficacy of breast cancer treatment regimens and mitigating drug resistance as well as providing a basis for potential novel therapeutic modalities for breast cancer.

摘要

mTOR的激活与乳腺癌的发生和发展有关。mTOR抑制在乳腺癌中显示出有前景的抗肿瘤作用;然而,其作用受到多种反馈机制的影响。其中一种机制是乳腺癌细胞中mTOR通路的上调。尽管mTOR激活在乳腺癌中的作用已得到确立,但mTOR总蛋白的状态及其对肿瘤行为和治疗反应的影响仍知之甚少。此外,正常和癌性乳腺细胞中mTOR蛋白降解的机制在很大程度上仍然未知。我们和其他人发现,与非恶性对应物相比,乳腺癌细胞中mTOR总蛋白水平升高。我们在乳腺癌细胞中检测到mTOR蛋白的蛋白水解缺陷,这至少可以部分解释这些细胞中mTOR蛋白的高水平。我们表明,在MCF-7乳腺癌细胞中用二甲双胍处理可诱导mTOR降解并将该蛋白隔离在核周区域。这些细胞中mTOR蛋白水平的降低与这些细胞增殖和迁移潜能的同时抑制呈正相关。这些发现为二甲双胍在乳腺癌治疗中的作用提供了一种新机制。了解负责乳腺癌中mTOR水平的蛋白水解机制可能为提高乳腺癌治疗方案的疗效、减轻耐药性以及为乳腺癌潜在的新治疗方式提供基础铺平道路。

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