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首页> 外文期刊>Cancer letters >A synthetic chalcone, 2 '-hydroxy-2,3,5 '-trimethoxychalcone triggers unfolded protein response-mediated apoptosis in breast cancer cells
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A synthetic chalcone, 2 '-hydroxy-2,3,5 '-trimethoxychalcone triggers unfolded protein response-mediated apoptosis in breast cancer cells

机译:合成的查尔酮,2'-羟基-2,3,5'-三甲氧基查尔酮触发乳腺癌细胞中未反应的蛋白反应介导的凋亡

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摘要

The primary aim of this study was to find novel chemopreventive agents effective against breast cancer. Endoplasmic reticulum (ER) stress can induce apoptosis through the unfolded protein response (UPR). 2'-Hydroxy-2,3,5'-trimethoxychalcone (DK143) is a synthetic flavonoid derivative. The present study provides evidence supporting the role of the UPR in mediating the apoptotic effect of DK143. Treatment with DK143 triggered apoptosis through the activation of the caspase pathway in MDA-MB-231 breast cancer cells without affecting viability of MCF10A non-transformed breast epithelial cells. Further analysis revealed that DK143 produced reactive oxygen species (ROS) in MDA-MB-231 cells, but not in MCF10A cells, and upregulated the expression of ER stress sensors, including GRP78/BiP, IRE1 alpha, CHOP, and Bim in MDA-MB-231 cells. In addition, UPR-related transcription factors, XBP-1 and CHOP, were activated by DK143. Moreover, silencing of IRE1 alpha or CHOP by corresponding siRNA molecules attenuated DK143-induced apoptosis. Furthermore, DK143 suppressed mouse tumor growth in vivo. These results demonstrate that promoting ER stress in breast cancer cells via UPR induction might be a promising strategy for developing new chemotherapeutic or chemopreventive agents for breast cancer. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
机译:这项研究的主要目的是找到对乳腺癌有效的新型化学预防剂。内质网(ER)应激可通过未折叠的蛋白应答(UPR)诱导凋亡。 2'-羟基-2,3,5'-三甲氧基查尔酮(DK143)是合成的类黄酮衍生物。本研究提供证据支持UPR在介导DK143的凋亡效应中的作用。 DK143处理可通过激活MDA-MB-231乳腺癌细胞中的半胱天冬酶途径触发凋亡,而不会影响MCF10A未转化的乳腺癌上皮细胞的活力。进一步的分析表明,DK143在MDA-MB-231细胞中产生活性氧(ROS),但在MCF10A细胞中不产生,并且上调了ER应激传感器的表达,包括GRP78 / BiP,IRE1 alpha,CHOP和Bim在MDA- MB-231细胞。此外,DK143激活了UPR相关的转录因子XBP-1和CHOP。此外,相应的siRNA分子使IRE1 alpha或CHOP沉默,从而减弱了DK143诱导的细胞凋亡。此外,DK143在体内抑制小鼠肿瘤的生长。这些结果表明,通过UPR诱导促进乳腺癌细胞内质网应激可能是开发新的乳腺癌化学疗法或化学预防剂的有前途的策略。 (C)2015 Elsevier Ireland Ltd.保留所有权利。

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