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PQ1,一种喹啉衍生物,通过激活半胱天冬酶-8 和半胱天冬酶-9,诱导 T47D 乳腺癌细胞凋亡。

PQ1, a quinoline derivative, induces apoptosis in T47D breast cancer cells through activation of caspase-8 and caspase-9.

机构信息

Department of Biochemistry, Kansas State University, K244 Mosier Hall, 1800 Denison Avenue, Manhattan, KS 66506, USA.

出版信息

Apoptosis. 2013 Sep;18(9):1071-82. doi: 10.1007/s10495-013-0855-1.

DOI:10.1007/s10495-013-0855-1
PMID:23677255
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3735622/
Abstract

Apoptosis, a programmed cell death, is an important control mechanism of cell homeostasis. Deficiency in apoptosis is one of the key features of cancer cells, allowing cells to escape from death. Activation of apoptotic signaling pathway has been a target of anti-cancer drugs in an induction of cytotoxicity. PQ1, 6-methoxy-8-[(3-aminopropyl)amino]-4-methyl-5-(3-trifluoromethylphenyloxy)quinoline, has been reported to decrease the viability of cancer cells and attenuate xenograft tumor growth. However, the mechanism of the anti-cancer effect is still unclear. To evaluate whether the cytotoxicity of PQ1 is related to induction of apoptosis, the effect of PQ1 on apoptotic pathways was investigated in T47D breast cancer cells. PQ1-treated cells had an elevation of cleaved caspase-3 compared to controls. Studies of intrinsic apoptotic pathway showed that PQ1 can activate the intrinsic checkpoint protein caspase-9, enhance the level of pro-apoptotic protein Bax, and release cytochrome c from mitochondria to cytosol; however, PQ1 has no effect on the level of anti-apoptotic protein Bcl-2. Further studies also demonstrated that PQ1 can activate the key extrinsic player, caspase-8. Pre-treatment of T47D cells with caspase-8 or caspase-9 inhibitor suppressed the cell death induced by PQ1, while pre-treatment with caspase-3 inhibitor completely counteracted the effect of PQ1 on cell viability. This report provides evidence that PQ1 induces cytotoxicity via activation of both caspase-8 and caspase-9 in T47D breast cancer cells.

摘要

细胞凋亡是一种程序性细胞死亡,是细胞内稳态的重要调控机制。凋亡缺陷是癌细胞的一个关键特征,使细胞能够逃避死亡。激活凋亡信号通路一直是抗癌药物诱导细胞毒性的靶点。PQ1(6-甲氧基-8-[(3-氨基丙基)氨基]-4-甲基-5-(3-三氟甲基苯氧基)喹啉)已被报道能降低癌细胞的活力并减弱异种移植肿瘤的生长。然而,其抗癌作用的机制尚不清楚。为了评估 PQ1 的细胞毒性是否与诱导细胞凋亡有关,研究了 PQ1 对 T47D 乳腺癌细胞中凋亡途径的影响。与对照组相比,PQ1 处理的细胞中 cleaved caspase-3 升高。对内在凋亡途径的研究表明,PQ1 可以激活内在检查点蛋白 caspase-9,增强促凋亡蛋白 Bax 的水平,并将细胞色素 c 从线粒体释放到细胞质中;然而,PQ1 对凋亡蛋白 Bcl-2 的水平没有影响。进一步的研究还表明,PQ1 可以激活关键的外在效应因子 caspase-8。用 caspase-8 或 caspase-9 抑制剂预处理 T47D 细胞可抑制 PQ1 诱导的细胞死亡,而用 caspase-3 抑制剂预处理则完全抵消了 PQ1 对细胞活力的影响。本报告提供的证据表明,PQ1 通过激活 T47D 乳腺癌细胞中的 caspase-8 和 caspase-9 诱导细胞毒性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b2a/3735622/a378eda8cbe6/nihms481038f9.jpg
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