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查耳酮类化合物抑制 AURKA 及其介导的乳腺癌细胞转移和多药耐药。

Chalcones Repressed the AURKA and MDR Proteins Involved in Metastasis and Multiple Drug Resistance in Breast Cancer Cell Lines.

机构信息

Biotechnology Unit, University of Ribeirão Preto, SP, Av. Costábile Romano, 2201, Ribeirão Preto, SP, CEP 14096-900, Brazil.

Department of Biomedical and Diagnostic Sciences, College of Veterinary Medicine, University of Tennessee, Knoxville, TN 37996, USA.

出版信息

Molecules. 2018 Aug 13;23(8):2018. doi: 10.3390/molecules23082018.

Abstract

In the present investigation, -chalcone and licochalcone A were tested against MCF-7 and BT-20 breast cancer cell lines for anti-tumor activity. We found that both chalcones down regulated important genes associated to cancer development and inhibited cell migration of metastatic cells (BT-20). Finally, we observed that licochalcone A reduces the MDR-1 protein, while both chalcones suppress the AURKA protein in a dose-dependent manner. In conclusion, we observed the -chalcone and licochalcone A affected the cell viability of breast cancer cell lines MCF-7 and BT-20 and presents anti-metastatic and anti-resistance potential, by the repression of AUKA and MDR-1 proteins.

摘要

在本研究中,我们测试了查尔酮和甘草查尔酮 A 对 MCF-7 和 BT-20 乳腺癌细胞系的抗肿瘤活性。我们发现,这两种查尔酮都下调了与癌症发展相关的重要基因,并抑制了转移性细胞(BT-20)的迁移。最后,我们观察到甘草查尔酮 A 降低了 MDR-1 蛋白,而这两种查尔酮均以剂量依赖的方式抑制 AURKA 蛋白。总之,我们观察到查尔酮和甘草查尔酮 A 通过抑制 AURKA 和 MDR-1 蛋白的表达,影响 MCF-7 和 BT-20 乳腺癌细胞系的细胞活力,表现出抗转移和抗耐药的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81bb/6222917/997a9e9ee0de/molecules-23-02018-g001.jpg

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