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首页> 外文期刊>OncoTargets and therapy >Grape seed procyanidin B2 promotes the autophagy and apoptosis in colorectal cancer cells via regulating PI3K/Akt signaling pathway
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Grape seed procyanidin B2 promotes the autophagy and apoptosis in colorectal cancer cells via regulating PI3K/Akt signaling pathway

机译:葡萄籽原花青素B2通过调节PI3K / Akt信号通路促进大肠癌细胞自噬和凋亡

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Aim: Colorectal cancer (CRC) is a major malignancy in China, which is the critical risk of people health. Many natural herbs extracts have been found to exhibit good therapeutic effect on CRC. Our previous study found that grape seed procyanidins B2 (PB2) would induce CRC cell death. However, the molecular mechanism underlying its anti-tumor effect on CRC remains unclear. Thereby, this study aimed to investigate the anti-tumor mechanism of PB2 on CRC. Methods: CCK-8, western blotting, flow cytometry, qRT-PCR and animal study were used in the current study. Results: The in vitro and in vivo data demonstrated that PB2 could promote the apoptosis of CRC cells in a dose-dependent manner, which was significantly reversed by caspase 3 inhibitor. Meanwhile, PB2 dose-dependently induced autophagy in CRC cells, which was markedly attenuated by autophagy inhibitor 3-MA. In addition, PB2 dose-dependently inhibited the expressions of p-PI3K, p-Akt and p-mTOR in the cells. Conclusion: PB2 dose-dependently induced apoptosis and autophagy in CRC cells via downregulation of PI3K/Akt pathway. This study provided the experimental basis for further development of PB2 as a new effective anticancer drug for the patients with CRC.
机译:目的:大肠癌(CRC)是中国的主要恶性肿瘤,是人们健康的重大风险。已经发现许多天然草药提取物对CRC表现出良好的治疗作用。我们先前的研究发现葡萄籽原花青素B2(PB2)会诱导CRC细胞死亡。然而,其对CRC的抗肿瘤作用的分子机制仍然不清楚。因此,本研究旨在探讨PB2对CRC的抗肿瘤机制。方法:本研究采用CCK-8,蛋白质印迹,流式细胞术,qRT-PCR和动物研究。结果:体外和体内数据表明,PB2可以剂量依赖的方式促进CRC细胞的凋亡,而caspase 3抑制剂可逆转该作用。同时,PB2剂量依赖性地诱导了CRC细胞中的自噬,这被自噬抑制剂3-MA明显减弱。另外,PB2剂量依赖性地抑制细胞中p-PI3K,p-Akt和p-mTOR的表达。结论:PB2通过下调PI3K / Akt途径剂量依赖性地诱导CRC细胞凋亡和自噬。该研究为进一步开发PB2作为CRC患者的新型有效抗癌药物提供了实验依据。

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