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橙皮素通过引发活性氧积累和激活ASK1/JNK信号通路诱导乳腺癌细胞凋亡。

Hesperetin Induces Apoptosis in Breast Carcinoma by Triggering Accumulation of ROS and Activation of ASK1/JNK Pathway.

作者信息

Palit Shreyasi, Kar Susanta, Sharma Gunjan, Das Pijush K

机构信息

Infectious Diseases and Immunology Division, CSIR-Indian Institute of Chemical Biology, Kolkata, India.

出版信息

J Cell Physiol. 2015 Aug;230(8):1729-39. doi: 10.1002/jcp.24818.

Abstract

Hesperetin, a flavanone glycoside predominantly found in citrus fruits, exhibits a wide array of biological properties. In the present study hesperetin exhibited a significant cytotoxic effect in human breast carcinoma MCF-7 cells in a concentration- and time-dependent manner without affecting normal (HMEC) as well as immortalized normal mammary epithelial cells (MCF-10A). The cytotoxic effect of hesperetin was due to the induction of apoptosis as evident from the phosphatidyl-serine externalization, DNA fragmentation, caspase-7 activation, and PARP cleavage. Apoptosis was associated with caspase-9 activation, mitochondrial membrane potential loss, release of cytochrome c, and increase in Bax:Bcl-2 ratio. Pre-treatment with caspase-9 specific inhibitor (Z-LEHD-fmk) markedly attenuated apoptosis suggesting an involvement of intrinsic mitochondrial apoptotic cascade. Further, DCFDA flow-cytometric analysis revealed triggering of ROS in a time-dependent manner. Pre-treatment with ROS scavenger N-acetylcysteine (NAC) and glutathione markedly abrogated hesperetin-mediated apoptosis whereas carbonyl cyanide m-chlorophenylhydrazone (CCCP) pretreatment along with DHR123-based flow-cytometry indicated the generation of cytosolic ROS. Profiling of MAPKs revealed activation of JNK upon hesperetin treatment which was abrogated upon NAC pre-treatment. Additionally, inhibition of JNK by SP600125 significantly reversed hesperetin-mediated apoptosis. The activation of JNK was associated with the activation of ASK1. Silencing of ASK1 resulted in significant attenuation of JNK activation as well as reversed the hesperetin-mediated apoptosis suggesting that hesperetin-mediated apoptosis of MCF-7 cells involves accumulation of ROS and activation of ASK1/JNK pathway. In addition, hesperetin also induced apoptosis in triple negative breast cancer MDA-MB-231 cells via intrinsic pathway via activation of caspase -9 and -3 and increase in Bax:Bcl-2 ratio.

摘要

橙皮素是一种主要存在于柑橘类水果中的黄酮糖苷,具有广泛的生物学特性。在本研究中,橙皮素对人乳腺癌MCF-7细胞表现出显著的细胞毒性作用,且呈浓度和时间依赖性,同时不影响正常(HMEC)以及永生化正常乳腺上皮细胞(MCF-10A)。从磷脂酰丝氨酸外化、DNA片段化、半胱天冬酶-7激活和聚(ADP-核糖)聚合酶裂解可明显看出,橙皮素的细胞毒性作用是由于诱导了细胞凋亡。细胞凋亡与半胱天冬酶-9激活、线粒体膜电位丧失、细胞色素c释放以及Bax:Bcl-2比值增加有关。用半胱天冬酶-9特异性抑制剂(Z-LEHD-fmk)预处理可显著减弱细胞凋亡,表明内在线粒体凋亡级联反应参与其中。此外,DCFDA流式细胞术分析显示以时间依赖性方式引发了活性氧(ROS)。用ROS清除剂N-乙酰半胱氨酸(NAC)和谷胱甘肽预处理可显著消除橙皮素介导的细胞凋亡,而羰基氰化物间氯苯腙(CCCP)预处理以及基于DHR123的流式细胞术表明产生了胞质ROS。丝裂原活化蛋白激酶(MAPKs)分析显示,橙皮素处理后JNK被激活,而NAC预处理可消除这种激活。此外,用SP600125抑制JNK可显著逆转橙皮素介导的细胞凋亡。JNK的激活与凋亡信号调节激酶1(ASK1)的激活有关。敲低ASK1可导致JNK激活显著减弱,并逆转橙皮素介导的细胞凋亡,这表明橙皮素介导的MCF-7细胞凋亡涉及ROS的积累以及ASK1/JNK途径的激活。此外,橙皮素还通过激活半胱天冬酶-9和-3以及增加Bax:Bcl-2比值,经内在途径诱导三阴性乳腺癌MDA-MB-231细胞凋亡。

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