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钌(II)-芳烃亚氨基膦烷化合物对三阴性乳腺癌细胞抗癌作用及其机制的研究

Investigation of the Effects and Mechanisms of Anticancer Action of a Ru(II)-Arene Iminophosphorane Compound in Triple Negative Breast Cancer Cells.

作者信息

Nayeem Nazia, Yeasmin Arefa, Cobos Samantha N, Younes Ali, Hubbard Karen, Contel Maria

机构信息

Department of Chemistry and Brooklyn College Cancer Center, Brooklyn College, The City University of New York, Brooklyn, NY, 11210, USA.

Biology, Chemistry and Biochemistry PhD Programs, The Graduate Center, The City University of New York, New York, NY, 10016, USA.

出版信息

ChemMedChem. 2021 Nov 5;16(21):3280-3292. doi: 10.1002/cmdc.202100325. Epub 2021 Aug 24.

Abstract

Triple negative breast cancer (TNBC) is one of the breast cancers with poorer prognosis and survival rates. TNBC has a disproportionally high incidence and mortality in women of African descent. We report on the evaluation of Ru-IM (1), a water-soluble organometallic ruthenium compound, in TNBC cell lines derived from patients of European (MDA-MB-231) and African (HCC-1806) ancestry (including IC values, cellular and organelle uptake, cell death pathways, cell cycle, effects on migration, invasion, and angiogenesis, a preliminary proteomic analysis, and an NCI 60 cell-line panel screen). 1 was previously found highly efficacious in MDA-MB-231 cells and xenografts, with little systemic toxicity and preferential accumulation in the tumor. We observe a similar profile for this compound in the two cell lines studied, which includes high cytotoxicity, apoptotic behavior and potential antimetastatic and antiangiogenic properties. Cytokine M-CSF, involved in the PI3/AKT pathway, shows protein expression inhibition with exposure to 1. We also demonstrate a p53 independent mechanism of action.

摘要

三阴性乳腺癌(TNBC)是预后和生存率较差的乳腺癌之一。TNBC在非洲裔女性中的发病率和死亡率异常高。我们报告了对Ru-IM(1)的评估,Ru-IM是一种水溶性有机金属钌化合物,用于评估源自欧洲(MDA-MB-231)和非洲(HCC-1806)血统患者的TNBC细胞系(包括半数抑制浓度、细胞及细胞器摄取、细胞死亡途径、细胞周期、对迁移、侵袭和血管生成的影响、初步蛋白质组学分析以及NCI 60细胞系面板筛选)。1先前已被发现对MDA-MB-231细胞和异种移植瘤具有高效性,几乎没有全身毒性且在肿瘤中优先蓄积。我们在研究的这两种细胞系中观察到该化合物具有相似的特性,包括高细胞毒性、凋亡行为以及潜在的抗转移和抗血管生成特性。参与PI3/AKT途径的细胞因子M-CSF在暴露于1时显示出蛋白表达抑制。我们还证明了一种不依赖p53的作用机制。

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