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沉默调节蛋白1依赖性白藜芦醇对乳腺癌细胞的细胞毒性和促分化活性。

Sirtuin 1-dependent resveratrol cytotoxicity and pro-differentiation activity on breast cancer cells.

作者信息

Deus Cláudia M, Serafim Teresa L, Magalhães-Novais Silvia, Vilaça Andreia, Moreira Ana C, Sardão Vilma A, Cardoso Susana M, Oliveira Paulo J

机构信息

CNC - Center for Neuroscience and Cell Biology, University of Coimbra, UC Biotech Building (Lot 8A), Biocant Park, 3060-197, Cantanhede, Portugal.

Department of Life Sciences, School of Sciences and Technology, University of Coimbra, 3004-517, Coimbra, Portugal.

出版信息

Arch Toxicol. 2017 Mar;91(3):1261-1278. doi: 10.1007/s00204-016-1784-x. Epub 2016 Jun 29.

Abstract

Sirtuins regulate several processes associated with tumor development. Resveratrol was shown to stimulate sirtuin 1 and 3 (SIRT1/3) activities and to result in cytotoxicity for some tumor types. The relationship between modulation of sirtuin activities, cellular metabolic remodeling and resveratrol cytotoxicity mechanism on breast cancer cells is still an open question. Here, we evaluated whether sirtuin 1 and 3 are involved in resveratrol toxicity and whether resveratrol leads to a metabolic remodeling and cell differentiation. Results using the Extracellular Flux Analyzer indicated that resveratrol inhibits mitochondrial respiration in breast cancer cells. We also demonstrated here for the first time that resveratrol cytotoxic effects on breast cancer cells were modulated by SIRT1 and also involved mitochondrial complex I inhibition. Importantly, we also demonstrated that resveratrol reduced the pool of breast cancer cells with stemness markers through a SIRT1-dependent mechanism. Our data highlights the role of SIRT1 in regulating resveratrol induced differentiation and/or toxicity in breast cancer cells.

摘要

沉默调节蛋白调控与肿瘤发展相关的多个过程。白藜芦醇已被证明可刺激沉默调节蛋白1和3(SIRT1/3)的活性,并对某些肿瘤类型产生细胞毒性。沉默调节蛋白活性的调节、细胞代谢重塑与白藜芦醇对乳腺癌细胞的细胞毒性机制之间的关系仍是一个悬而未决的问题。在此,我们评估了沉默调节蛋白1和3是否参与白藜芦醇的毒性作用,以及白藜芦醇是否会导致代谢重塑和细胞分化。使用细胞外通量分析仪的结果表明,白藜芦醇可抑制乳腺癌细胞中的线粒体呼吸。我们在此还首次证明,白藜芦醇对乳腺癌细胞的细胞毒性作用受SIRT1调节,并且还涉及线粒体复合物I的抑制。重要的是,我们还证明白藜芦醇通过一种依赖SIRT1的机制减少了具有干性标志物的乳腺癌细胞池。我们的数据突出了SIRT1在调节白藜芦醇诱导的乳腺癌细胞分化和/或毒性中的作用。

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