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新型非甾体类抗炎药尼氟灭酸的 Co(II)和 Ni(II)配合物对人乳腺癌 MCF-7 细胞的体外抗癌活性。

In Vitro Anticancer Activity of Novel Co(II) and Ni(II) Complexes of Non-steroidal Anti-inflammatory Drug Niflumic Acid Against Human Breast Adenocarcinoma MCF-7 Cells.

机构信息

Department of Chemistry, Faculty of Arts and Sciences, Erzincan Binali Yıldırım University, 24100, Erzincan, Turkey.

Department of Biology, Faculty of Arts and Sciences, Erzincan Binali Yıldırım University, 24100, Erzincan, Turkey.

出版信息

Cell Biochem Biophys. 2021 Dec;79(4):729-746. doi: 10.1007/s12013-021-00984-z. Epub 2021 Apr 29.

Abstract

Herein, we report the synthesis, characterization and anticancer activity of six novel complexes of non-steroidal anti-inflammatory drug niflumic acid with Co(II) and Ni(II). In vitro cytotoxicity screening in MCF-7, HepG2 and HT-29 cancer cell lines showed that the complex 3 [Co(nif)(met)(4-pic)] and complex 6 [Ni(nif)(met)(4-pic)] among all the complexes exhibited the highest cytotoxicity against MCF-7 cells with IC values of 11.14 µM and, 41.47 µM, respectively. Besides, all the complexes exhibited significantly higher selectivity towards mouse fibroblast 3T3L1 cells. Further mechanistic studies with both complexes on MCF-7 cells revealed their cytotoxic action through the mitochondrial-dependent apoptotic pathway causing an increase oxidative/nitrosative stress, decrease in mitochondrial membrane potential (ΔΨm), inducing the multicaspase activation and arresting the cell cycle at S phase. q-PCR analysis resulted in an increase in the expression of the apoptotic marker proteins bax, p53 and caspase-3 and -8 in MCF-7 cells, but a decrease in the expression of antiapoptotic bcl-2 gene. Moreover, both complexes induced the apoptosis through the inhibition of PI3K/Akt signaling pathway by decreasing the expression of PI3K and increasing dephosphorylation form of Akt protein. These results provide a significant contribution to the explanation of the anticancer mechanisms of these complexes in MCF-7 cells.

摘要

在此,我们报告了非甾体抗炎药尼氟灭酸与 Co(II)和 Ni(II)的六个新配合物的合成、表征和抗癌活性。在 MCF-7、HepG2 和 HT-29 癌细胞系中的体外细胞毒性筛选表明,所有配合物中,配合物 3 [Co(nif)(met)(4-pic)]和配合物 6 [Ni(nif)(met)(4-pic)]对 MCF-7 细胞表现出最高的细胞毒性,IC 值分别为 11.14 µM 和 41.47 µM。此外,所有配合物对小鼠成纤维细胞 3T3L1 细胞表现出显著更高的选择性。对 MCF-7 细胞的这两种配合物进行的进一步机制研究表明,它们通过线粒体依赖性凋亡途径发挥细胞毒性作用,导致氧化/硝化应激增加,线粒体膜电位(ΔΨm)降低,多半胱氨酸酶激活,并使细胞周期停滞在 S 期。q-PCR 分析导致 MCF-7 细胞中凋亡标记蛋白 bax、p53 和 caspase-3 的表达增加,而抗凋亡 bcl-2 基因的表达减少。此外,两种配合物通过抑制 PI3K/Akt 信号通路,降低 PI3K 的表达并增加 Akt 蛋白的去磷酸化形式,诱导细胞凋亡。这些结果为解释这些配合物在 MCF-7 细胞中的抗癌机制提供了重要贡献。

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