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肝细胞癌中的可变剪接

Alternative Splicing in Hepatocellular Carcinoma.

作者信息

Lee Seung Eun, Alcedo Karel P, Kim Hong Jin, Snider Natasha T

机构信息

Department of Surgery, Chung-Ang University, Seoul, Korea; Department of Cell Biology and Physiology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.

Department of Cell Biology and Physiology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.

出版信息

Cell Mol Gastroenterol Hepatol. 2020;10(4):699-712. doi: 10.1016/j.jcmgh.2020.04.018. Epub 2020 May 8.

Abstract

Hepatocellular carcinoma (HCC) accounts for the majority of primary liver cancer cases, with more than 850,000 new diagnoses per year globally. Recent trends in the United States have shown that liver cancer mortality has continued to increase in both men and women, while 5-year survival remains below 20%. Understanding key mechanisms that drive chronic liver disease progression to HCC can reveal new therapeutic targets and biomarkers for early detection of HCC. In that regard, many studies have underscored the importance of alternative splicing as a source of novel HCC prognostic markers and disease targets. Alternative splicing of pre-mRNA provides functional diversity to the genome, and endows cells with the ability to rapidly remodel the proteome. Genes that control fundamental processes, such as metabolism, cell proliferation, and apoptosis, are altered globally in HCC by alternative splicing. This review highlights the major splicing factors, RNA binding proteins, transcriptional targets, and signaling pathways that are of key relevance to HCC. We highlight primary research from the past 3-5 years involving functional interrogation of alternative splicing in rodent and human liver, using both large-scale transcriptomic and focused mechanistic approaches. Because this is a rapidly advancing field, we anticipate that it will be transformative for the future of basic liver biology, as well as HCC diagnosis and management.

摘要

肝细胞癌(HCC)占原发性肝癌病例的大多数,全球每年有超过85万例新诊断病例。美国最近的趋势表明,肝癌死亡率在男性和女性中都持续上升,而5年生存率仍低于20%。了解驱动慢性肝病进展为HCC的关键机制可以揭示新的治疗靶点和用于早期检测HCC的生物标志物。在这方面,许多研究强调了可变剪接作为新型HCC预后标志物和疾病靶点来源的重要性。前体mRNA的可变剪接为基因组提供了功能多样性,并赋予细胞快速重塑蛋白质组的能力。在HCC中,控制诸如代谢、细胞增殖和凋亡等基本过程的基因通过可变剪接在整体上发生改变。本综述重点介绍了与HCC密切相关的主要剪接因子、RNA结合蛋白、转录靶点和信号通路。我们重点介绍了过去3至5年的主要研究,这些研究使用大规模转录组学和聚焦机制的方法,对啮齿动物和人类肝脏中的可变剪接进行了功能研究。由于这是一个快速发展的领域,我们预计它将对基础肝脏生物学以及HCC的诊断和管理的未来产生变革性影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f62b/7490524/d9afe13eb3f6/gr1.jpg

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