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评价再利用药物辛伐他汀/百里醌联合用药对乳腺癌细胞系的增强细胞毒性作用。

Evaluation of Enhanced Cytotoxicity Effect of Repurposed Drug Simvastatin/Thymoquinone Combination against Breast Cancer Cell Line.

机构信息

Department of Biotechnology, Jaypee Institute of Information Technology, A-10, Noida, Sector 62, U.P., 201309, India.

出版信息

Cardiovasc Hematol Agents Med Chem. 2024;22(3):348-366. doi: 10.2174/0118715257259037231012182741.

Abstract

INTRODUCTION

Repurposing of drugs for their anticancer potential is gaining a lot of importance in drug discovery.

AIMS

The present study aims to explore the potential of Simvastatin (SIM), a drug used in the treatment of high cholesterol, and Thymoquinone () (THY) for its anti-cancer activity on breast cancer cell lines. Thymoquinone is reported to have many potential medicinal properties exhibiting antioxidant, antiinflammatory, anti-cancer, activities like inhibition of tissue growth and division.

METHODS

In this analysis, we explored the inhibitory effects of the combination of Simvastatin ad Thymoquinone on two breast cancer cell lines viz MCF-7 and MDA-MB-231 cells. The combined effect of Simvastatin and Thymoquinone on Cell viability, Colony formation, Cell migration, and orientation of more programmed cell death was studied. Cell cycle arrest in the G2/M phase was concomitant with the combined effect of SIM and THY persuading apoptosis and generating reactive oxygen species (ROS).

RESULTS

The cell cycle arrest with combined treatment was observed that only 1.8% and 1.1% cells gated in G2/M phase in MCF-7 & MDA-MB-231 cell. An increased apoptosis was observed when cells were treated in combination which was about 76.20% and 58.15% respectively for MCF-7 and MDA-MB-231 cells.

CONCLUSION

It was concluded that the combined effect of simvastatin and thymoquinone stimulates apoptosis in breast cancer cells.

摘要

简介

药物的重新定位以挖掘其抗癌潜力在药物发现中变得越来越重要。

目的

本研究旨在探索辛伐他汀(SIM)——一种用于治疗高胆固醇的药物——和姜黄素(THY)在乳腺癌细胞系中的抗癌活性潜力。据报道,姜黄素具有许多潜在的药用特性,具有抗氧化、抗炎、抗癌作用,如抑制组织生长和分裂。

方法

在这项分析中,我们探索了辛伐他汀和姜黄素联合对两种乳腺癌细胞系 MCF-7 和 MDA-MB-231 细胞的抑制作用。研究了辛伐他汀和姜黄素联合对细胞活力、集落形成、细胞迁移和程序性细胞死亡方向的影响。细胞周期在 G2/M 期的停滞伴随着 SIM 和 THY 的联合作用,促使细胞凋亡并产生活性氧(ROS)。

结果

联合治疗观察到细胞周期停滞,仅 MCF-7 和 MDA-MB-231 细胞中有 1.8%和 1.1%的细胞进入 G2/M 期。当细胞联合治疗时,观察到细胞凋亡增加,分别约为 MCF-7 和 MDA-MB-231 细胞的 76.20%和 58.15%。

结论

辛伐他汀和姜黄素的联合作用刺激乳腺癌细胞凋亡。

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