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肝细胞癌中葡萄糖代谢的重编程:进展与展望

Reprogramming of glucose metabolism in hepatocellular carcinoma: Progress and prospects.

作者信息

Shang Run-Ze, Qu Shi-Bin, Wang De-Sheng

机构信息

Run-Ze Shang, Shi-Bin Qu, De-Sheng Wang, Department of Hepatobiliary Surgery, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, Shaanxi Province, China.

出版信息

World J Gastroenterol. 2016 Dec 7;22(45):9933-9943. doi: 10.3748/wjg.v22.i45.9933.

Abstract

Hepatocellular carcinoma (HCC) is one of the most lethal cancers, and its rate of incidence is rising annually. Despite the progress in diagnosis and treatment, the overall prognoses of HCC patients remain dismal due to the difficulties in early diagnosis and the high level of tumor invasion, metastasis and recurrence. It is urgent to explore the underlying mechanism of HCC carcinogenesis and progression to find out the specific biomarkers for HCC early diagnosis and the promising target for HCC chemotherapy. Recently, the reprogramming of cancer metabolism has been identified as a hallmark of cancer. The shift from the oxidative phosphorylation metabolic pathway to the glycolysis pathway in HCC meets the demands of rapid cell proliferation and offers a favorable microenvironment for tumor progression. Such metabolic reprogramming could be considered as a critical link between the different HCC genotypes and phenotypes. The regulation of metabolic reprogramming in cancer is complex and may occur genetic mutations and epigenetic modulations including oncogenes, tumor suppressor genes, signaling pathways, noncoding RNAs, and glycolytic enzymes . Understanding the regulatory mechanisms of glycolysis in HCC may enrich our knowledge of hepatocellular carcinogenesis and provide important foundations in the search for novel diagnostic biomarkers and promising therapeutic targets for HCC.

摘要

肝细胞癌(HCC)是最致命的癌症之一,其发病率逐年上升。尽管在诊断和治疗方面取得了进展,但由于早期诊断困难以及肿瘤侵袭、转移和复发程度高,HCC患者的总体预后仍然不佳。迫切需要探索HCC发生和发展的潜在机制,以找出HCC早期诊断的特异性生物标志物和HCC化疗的有前景靶点。最近,癌症代谢重编程已被确定为癌症的一个标志。HCC中从氧化磷酸化代谢途径向糖酵解途径的转变满足了细胞快速增殖的需求,并为肿瘤进展提供了有利的微环境。这种代谢重编程可被视为不同HCC基因型和表型之间的关键联系。癌症中代谢重编程的调节是复杂的,可能发生基因突变和表观遗传调控,包括癌基因、肿瘤抑制基因、信号通路、非编码RNA和糖酵解酶。了解HCC中糖酵解的调控机制可能会丰富我们对肝细胞癌发生的认识,并为寻找新的诊断生物标志物和HCC有前景的治疗靶点提供重要基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8224/5143760/8b60fd2096f9/WJG-22-9933-g001.jpg

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