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首页> 外文期刊>Journal of oncology >Oleanolic Acid Induces Autophagy and Apoptosis via the AMPK-mTOR Signaling Pathway in Colon Cancer
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Oleanolic Acid Induces Autophagy and Apoptosis via the AMPK-mTOR Signaling Pathway in Colon Cancer

机译:OleAlic acid通过结肠癌中的AMPK-MTOR信号传导途径诱导自噬和细胞凋亡

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Aims . The purpose of this study was to explore the biological functions of the mTOR and AMPK signaling pathways in colon cancer (CC). The potential molecular mechanisms by which oleanolic acid (OA) induces autophagy and apoptosis were also investigated. Methods . The biological functions of mTOR were analyzed by GeneCards, the Search Tool for the Retrieval of Interacting Genes (STRING), and the Database for Annotation, Visualization and Integrated Discovery (DAVID). Least absolute shrinkage and selection operator (LASSO) regression analysis was used to obtain prognostic and survival data of CC patients from the Gene Expression Omnibus (GEO) database. The effects of OA on the CC cell lines HCT-116 and SW-480 were analyzed by CCK-8, colony formation assay, and high-content system (HCS) array scan. The apoptosis rate of SW-480 and HCT-116 cells was detected by flow cytometry. The mRNA and protein expression levels in HCT-116 and SW-480 cells and NCM-460 normal colonic epithelial cells were detected by RT-PCR and Western blotting. Results . mTOR was highly expressed in CC patients and acted as an oncogene. The AMPK signaling pathway mediated by mTOR predicted the poor prognosis of CC patients. OA effectively inhibited the proliferation and viability of CC cells. Furthermore, the apoptosis rate of CC cells was clearly increased following OA administration. Regarding the molecular mechanism of OA, the results indicated that mTOR and the antiapoptosis gene Bcl-2 were downregulated by OA. In addition, regulator genes of autophagy and apoptosis, including BAX, caspase-9, caspase-8, and caspase-3, were significantly upregulated by OA. Moreover, OA upregulated AMPK and its downstream proteins, including TSC2, BAX, Beclin 1, LC3B-II, and ULK1, to induce autophagy and apoptosis in CC cells. Conclusion . The findings from this study demonstrate that OA could effectively inhibit the proliferation and viability of CC cells. The anti-CC activity of OA is closely related to the activation of the AMPK-mTOR signaling pathway. Activation of AMPK and inhibition of mTOR are involved in the induction of autophagy and apoptosis by OA. OA induced autophagy and apoptosis mainly in an AMPK activation-dependent manner in CC cells.
机译:目标。本研究的目的是探讨结肠癌(CC)中MTOR和AMPK信号通路的生物学功能。还研究了OLEALOLIC酸(OA)诱导自噬和细胞凋亡的潜在分子机制。方法 。通过Genecards分析MTOR的生物学功能,用于检索交互基因(字符串)的搜索工具,以及用于注释,可视化和集成发现(DAVID)的数据库。最不绝对的收缩和选择操作员(套索)回归分析用于从基因表达综合(GEO)数据库中获得CC患者的预后和存活数据。通过CCK-8,菌落形成测定和高含量系统(HCS)阵列扫描,分析了OA对CC细胞系HCT-116和SW-480的影响。通过流式细胞术检测SW-480和HCT-116细胞的凋亡率。通过RT-PCR和Western印迹检测HCT-116和SW-480细胞中的mRNA和蛋白表达水平和NCM-460正常结肠上皮细胞。结果 。 MTOR在CC患者中高度表达,并作为癌基因。 MTOR介导的AMPK信号通路预测CC患者的预后差。 OA有效地抑制了CC细胞的增殖和活力。此外,OA给药后CC细胞的凋亡率明显增加。关于OA的分子机制,结果表明,MTOR和抗痘病基因Bcl-2通过OA下调。此外,通过OA显着上调了自噬和凋亡,包括Bax,Caspase-9,Caspase-8和Caspase-3的调节剂基因。此外,OA上调的AMPK及其下游蛋白质,包括TSC2,BAX,BECLIN 1,LC3B-II和ULK1,以在CC细胞中诱导自噬和凋亡。结论 。本研究的发现表明OA可以有效抑制CC细胞的增殖和活力。 OA的抗CC活性与AMPK-MTOR信号传导途径的激活密切相关。 AMPK的活化和对mTOR的抑制涉及OA的自噬和凋亡诱导。 OA诱导的自噬和凋亡主要是在CC细胞中的AMPK活化依赖性方式。

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