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肝细胞癌中与线粒体功能障碍相关的基因。

Mitochondrial dysfunction-related genes in hepatocellular carcinoma.

机构信息

Division of Hepatobiliary and Pancreatic Surgery, Department of Surgery, First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, Zhejiang Province, China.

出版信息

Front Biosci (Landmark Ed). 2013 Jun 1;18(3):1141-9. doi: 10.2741/4169.

Abstract

Mitochondria dysfunction is associated with apoptotic resistance and metabolism of tumor cells. Hepatocellular carcinoma (HCC) is a complex and heterogeneous tumor with multiple genetic aberrations. Certain gene mutations in mitochondria may lead to mitochondrial dysfunction. The p53 family plays a key role in the mitochondrial apoptosis pathway and acts as part of the molecular mechanisms underlying mitochondrial dysfunction in HCC. The novel genes found in the mitochondrial apoptosis signaling pathways, such as mfn2, play a role in the p53 network. In mitochondrial metabolism, expression of certain genes may be associated with apoptosis when they are involved in hepatocarcinogenesis. MicroRNAs have also been found to play a role in this process. Some genes may even exhibit multiple functions in the mitochondrial dysfunction of HCC. In HCC therapy, genes have also been found to influence the chemotherapeutic treatment by killing cells via the apoptosis pathway or autophagy. Investigation of mitochondrial dysfunction-related genes could potentially provide evidence for novel therapies that target HCC.

摘要

线粒体功能障碍与肿瘤细胞的抗凋亡和代谢有关。肝细胞癌 (HCC) 是一种复杂的异质性肿瘤,存在多种基因异常。线粒体中的某些基因突变可能导致线粒体功能障碍。p53 家族在线粒体凋亡途径中发挥关键作用,是 HCC 中线粒体功能障碍的分子机制的一部分。在线粒体凋亡信号通路中发现的新基因,如 mfn2,在 p53 网络中发挥作用。在线粒体代谢中,某些基因的表达在参与肝癌发生时可能与细胞凋亡有关。microRNAs 也被发现在此过程中发挥作用。一些基因甚至在 HCC 中线粒体功能障碍中表现出多种功能。在 HCC 治疗中,也发现某些基因通过凋亡途径或自噬杀死细胞,从而影响化疗治疗。研究与线粒体功能障碍相关的基因可能为针对 HCC 的新型治疗方法提供证据。

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