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二甲双胍对脂肪来源的基质细胞(ADSC)-乳腺癌细胞系相互作用的影响。

Effects of metformin on adipose-derived stromal cell (ADSC) - Breast cancer cell lines interaction.

机构信息

Department of Plastic and Reconstructive Surgery, Medical University of Vienna, Vienna, Austria.

Department of Vascular Surgery, Medical University of Vienna, Vienna, Austria.

出版信息

Life Sci. 2020 Nov 15;261:118371. doi: 10.1016/j.lfs.2020.118371. Epub 2020 Aug 31.

Abstract

AIMS

Metformin is a clinical drug administered to patients to treat type 2 diabetes mellitus that was found to be associated with a lower risk of occurrence of cancer and cancer-related death. The present study investigated the effects of metformin on human adipose-derived stromal cells (ADSC) - breast cancer cell line interactions.

MAIN METHODS

ADSCs grown from lipoaspirates were tested for growth-stimulating and migration-controlling activity on breast cancer cell lines after pretreatment with metformin. Furthermore, secreted proteins of ADSCs, phosphorylation of intracellular proteins and the effect of metformin on adipocytic differentiation of ADSCs were assayed.

KEY FINDINGS

Compared to breast cancer cell lines (4.0 ± 3.5% reduction of proliferation), 2 mM metformin significantly inhibited the proliferation of ADSC lines (19.2 ± 8.4% reduction of proliferation). This effect on ADSCs seems to be mediated by altered phosphorylation of GSK-3, CREB and PRAS40. Furthermore, treatment with metformin abolished the induction of differentiation of three ADSC lines to adipocytes. 1 and 2 mM metformin significantly impaired the migration of breast cancer cell lines MDA-MB-231 and MDA-MB-436 in scratch assays.

SIGNIFICANCE

Metformin showed low direct inhibitory effects on breast cancer cell lines at physiological concentrations but exerted a significant retardation of the growth and the adipocytic differentiation of ADSCs. Thus, the anticancer activity of metformin in breast cancer at physiological drug concentrations seems to be mediated by an indirect mechanism that lowers the supportive activity of ADSCs.

摘要

目的

二甲双胍是一种用于治疗 2 型糖尿病的临床药物,研究发现其与癌症发生风险降低和癌症相关死亡风险降低有关。本研究旨在探讨二甲双胍对人脂肪源基质细胞(ADSC)-乳腺癌细胞系相互作用的影响。

主要方法

用二甲双胍预处理后,检测从脂肪抽吸物中生长的 ADSC 对乳腺癌细胞系的生长刺激和迁移控制活性。此外,还检测了 ADSC 的分泌蛋白、细胞内蛋白的磷酸化以及二甲双胍对 ADSC 脂肪分化的影响。

主要发现

与乳腺癌细胞系相比(增殖减少 4.0±3.5%),2 mM 二甲双胍显著抑制 ADSC 系的增殖(增殖减少 19.2±8.4%)。这种对 ADSC 的作用似乎是通过改变 GSK-3、CREB 和 PRAS40 的磷酸化来介导的。此外,二甲双胍治疗消除了 3 种 ADSC 系向脂肪细胞分化的诱导。1 和 2 mM 二甲双胍显著抑制划痕试验中 MDA-MB-231 和 MDA-MB-436 乳腺癌细胞系的迁移。

意义

二甲双胍在生理浓度下对乳腺癌细胞系表现出低的直接抑制作用,但显著延缓 ADSC 的生长和脂肪分化。因此,二甲双胍在生理药物浓度下对乳腺癌的抗癌活性似乎是通过降低 ADSC 的支持活性的间接机制介导的。

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