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Terpinen-4-ol Induces Apoptosis in Human Nonsmall Cell Lung Cancer In Vitro and In Vivo

机译:Terpinen-4-ol在体内和体外诱导人非小细胞肺癌细胞凋亡。

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摘要

Terpinen-4-ol, a monoterpene component of the essential oils of several aromatic plants, exhibits antitumor effects. In this study, the antitumor effects of terpinen-4-ol and the cellular and molecular mechanisms responsible for it were evaluated and studied, respectively on human nonsmall cell lung cancer (NSCLC) cells. Our results indicated that terpinen-4-ol elicited a dose-dependent cytotoxic effect, as determined by MTT assay. Increased sub-G1 population and annexin-V binding, activation of caspases 9 and 3, cleavage of poly(ADPribose) polymerase (PARP), and a decrease of mitochondrial membrane potential (MMP) indicated involvement of the mitochondrial apoptotic pathway in terpinen-4-ol-treated A549 and CL1-0 cells. Elevation of the Bax/Bcl-2 ratio and a decrease in IAP family proteins XIAP and survivin were also observed following terpinen-4-ol treatment. Notably, terpinen-4-ol was able to increase p53 levels in A549 and CL1-0 cells. Diminution of p53 by RNA interference induced necrosis instead of apoptosis in A549 cells following terpinen-4-ol treatment, indicating that terpinen-4-ol-elicited apoptosis is p53-dependent. Moreover, intratumoral administration of terpinen-4-ol significantly suppressed the growth of s.c. A549 xenografts by inducing apoptosis, as confirmed by TUNEL assay. Collectively, these data provide insight into the molecular mechanisms underlying terpinen-4-ol-induced apoptosis in NSCLC cells, rendering this compound a potential anticancer drug for NSCLC.
机译:Terpinen-4-ol是几种芳香植物精油中的单萜成分,具有抗肿瘤作用。在这项研究中,分别评估和研究了萜品四醇对人非小细胞肺癌(NSCLC)细胞的抗肿瘤作用及其分子机制。我们的结果表明,如MTT分析所确定的那样,萜品四醇具有剂量依赖性的细胞毒性作用。亚G1族和膜联蛋白V的结合增加,胱天蛋白酶9和3的激活,聚(ADPribose)聚合酶(PARP)的裂解以及线粒体膜电位(MMP)的降低表明在Terpinen-4中涉及线粒体凋亡途径。 -ol处理的A549和CL1​​-0细胞。萜品醇-4-醇处理后,还观察到Bax / Bcl-2比升高,IAP家族蛋白XIAP和survivin降低。值得注意的是,萜品四醇能够提高A549和CL1​​-0细胞中的p53水平。萜品醇-4-醇处理后,RNA干扰减少p53诱导的A549细胞坏死而不是凋亡,这表明萜品醇-4-醇引起的凋亡是p53依赖性的。而且,瘤内给予萜品四-4-醇可显着抑制皮下生长。 TUNEL分析证实,A549可以通过诱导细胞凋亡来进行异种移植。总的来说,这些数据提供了对萜品醇-4-醇诱导的NSCLC细胞凋亡的分子机制的了解,使该化合物成为NSCLC的潜在抗癌药物。

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