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首页> 外文期刊>International journal of molecular medicine >Corosolic acid induces apoptotic cell death in HCT116 human colon cancer cells through a caspase-dependent pathway
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Corosolic acid induces apoptotic cell death in HCT116 human colon cancer cells through a caspase-dependent pathway

机译:胆固醇通过半胱天冬酶依赖性途径诱导HCT116人结肠癌细胞凋亡

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Corosolic acid (CA), a pentacyclic triterpene isolated from Lagerstroemia speciosa L. (also known as Banaba), has been shown to exhibit anticancer properties in various cancer cell lines. However, the anticancer activity of CA on human colorectal cancer cells and the underlying mechanisms remain to be elucidated. In this study, we investigated the effects of CA on cell viability and apoptosis in HCT116 human colon cancer cells. CA dose-dependently inhibited the viability of HCT116 cells. The typical hallmarks of apoptosis, such as chromatin condensation, a sub-G1?peak and phosphatidylserine externalization were detected by Hoechst?33342 staining, flow cytometry and Annexin?V staining following treatment with CA. Western blot analysis revealed that CA induced a decrease in the levels of procaspase-8, -9 and?-3 and the cleavage of poly(ADP-ribose) polymerase (PARP). The apoptotic cell death induced by CA was accompanied by the activation of caspase-8, -9 and?-3, which was completely abrogated by the pan-caspase inhibitor, z-VAD?FMK. Furthermore, CA upregulated the levels of pro-apoptotic proteins, such as Bax, Fas and FasL and downregulated the levels of anti-apoptotic proteins, such as Bcl-2 and survivin. Taken together, our data provide insight into the molecular mechanisms of CA-induced apoptosis in colorectal cancer (CRC), rendering this compound a potential anticancer agent for the treatment of CRC.
机译:熊果酸(CA)是一种从紫薇(又称香蕉)分离的五环三萜,已显示出在多种癌细胞系中的抗癌特性。然而,CA对人结肠直肠癌细胞的抗癌活性及其潜在机制仍有待阐明。在这项研究中,我们调查了CA对HCT116人结肠癌细胞的细胞活力和细胞凋亡的影响。 CA剂量依赖性抑制HCT116细胞的活力。用CA处理后,通过Hoechst?33342染色,流式细胞仪和Annexin?V染色检测到典型的凋亡标志物,例如染色质浓缩,亚G1峰和磷脂酰丝氨酸外在化。 Western印迹分析表明,CA诱导了procaspase-8,-9和β-3水平的降低以及聚(ADP-核糖)聚合酶(PARP)的裂解。 CA诱导的凋亡细胞死亡伴随着caspase-8,-9和α-3的活化,而泛半胱天冬酶抑制剂z-VADβFMK则完全消除了这种作用。此外,CA上调了促凋亡蛋白(例如Bax,Fas和FasL)的水平,并下调了抗凋亡蛋白(例如Bcl-2和survivin)的水平。综上所述,我们的数据提供了对CA诱导的结直肠癌(CRC)细胞凋亡的分子机制的见解,使该化合物成为治疗CRC的潜在抗癌药。

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