Genotoxicity Lab, Division of Toxicology, CSIR- Central Drug Research Institute, Sector -10, Jankipuram Extension, Lucknow, Uttar Pradesh, 226031, India.
National Institute of Pharmaceutical Education and Research, ITI compound, Raebareli, Uttar Pradesh, 229010, India.
Apoptosis. 2017 Oct;22(10):1246-1259. doi: 10.1007/s10495-017-1394-y.
Resveratrol (RES) is a natural polyphenol having anti-proliferative activity against breast cancer cells. RES in combination with other chemo modulatory agents, minimizes toxicity and increases efficacy of the treatment. Salinomycin (SAL), a monocarboxylic polyether ionophore is known for selectively targeting breast cancer stem cells. Purpose of the present study was to investigate whether RES in combination with SAL exerts synergistic anti-proliferative activity on breast cancer cells. We further evaluated the molecular mechanism behind SAL and RES mediated cell death. Cytotoxicity assay was performed to determine 50% inhibitory concentration (IC50) of SAL and RES in different human breast cancer cells (HBCCs). Drug synergism and combination index (CI) were calculated using CompuSyn software and effects of synergistic combinations (CI < 1) involving lower doses of SAL and RES were selected for further studies. This combination significantly induced apoptosis in HBCCs without affecting non tumorigenic human breast epithelial cells MCF-10A. Co-treatment enhanced apoptosis in MCF-7 cells via reactive oxygen species (ROS) mediated mitochondrial dysfunction. Oxidative stress disrupt redox homeostasis which altered antioxidant enzymes viz. CuZn Superoxide dismutase (SOD), MnSOD and catalase. Additionally, combination altered nuclear morphology, enhanced PARP cleavage and led to caspase activation. SAL and RES also synergistically modulated MAPK pathway. Study suggests that SAL and RES offer a novel combination approach for the treatment of breast cancer.
白藜芦醇(RES)是一种天然多酚,对乳腺癌细胞具有抗增殖活性。RES 与其他化疗调节剂联合使用,可以最大程度地降低毒性并提高治疗效果。萨利霉素(SAL)是一种单羧酸聚醚离子载体,已知可选择性靶向乳腺癌干细胞。本研究旨在探讨 RES 与 SAL 联合使用对乳腺癌细胞是否具有协同的抗增殖活性。我们进一步评估了 SAL 和 RES 介导细胞死亡的分子机制。通过细胞毒性测定来确定 SAL 和 RES 在不同人乳腺癌细胞(HBCCs)中的 50%抑制浓度(IC50)。使用 CompuSyn 软件计算药物协同作用和组合指数(CI),并选择具有协同作用(CI<1)的较低剂量 SAL 和 RES 组合进行进一步研究。该组合在不影响非致瘤性人乳腺上皮细胞 MCF-10A 的情况下,显著诱导 HBCC 凋亡。共处理通过活性氧(ROS)介导的线粒体功能障碍增强 MCF-7 细胞中的凋亡。氧化应激破坏了氧化还原稳态,改变了抗氧化酶,如 CuZn 超氧化物歧化酶(SOD)、MnSOD 和过氧化氢酶。此外,组合改变了核形态,增强了 PARP 切割,并导致 caspase 激活。SAL 和 RES 还协同调节 MAPK 通路。研究表明,SAL 和 RES 为治疗乳腺癌提供了一种新的联合方法。