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人类肝细胞癌中的表观遗传重塑。

Epigenetic remodelling in human hepatocellular carcinoma.

机构信息

Unit of Molecular Genetics of Complex Phenotypes, Bambino Gesù Children's Hospital, IRCCS, Viale S. Paolo, 15, 00146, Rome, Italy.

Department of Translational Stem Cell Biology, Research Institute of the Medical University of Varna, Varna, Bulgaria.

出版信息

J Exp Clin Cancer Res. 2022 Mar 24;41(1):107. doi: 10.1186/s13046-022-02297-2.

Abstract

Hepatocellular carcinoma (HCC) is the most frequent primary liver cancer, being the sixth most commonly diagnosed cancer and the fourth leading cause of cancer-related death. As other heterogeneous solid tumours, HCC results from a unique synergistic combination of genetic alterations mixed with epigenetic modifications.In HCC the patterns and frequencies of somatic variations change depending on the nearby chromatin. On the other hand, epigenetic alterations often induce genomic instability prone to mutations. Epigenetics refers to heritable states of gene expression without alteration to the DNA sequence itself and, unlike genetic changes, the epigenetic modifications are reversible and affect gene expression more extensively than genetic changes. Thus, studies of epigenetic regulation and the involved molecular machinery are greatly contributing to the understanding of the mechanisms that underline HCC onset and heterogeneity. Moreover, this knowledge may help to identify biomarkers for HCC diagnosis and prognosis, as well as future new targets for more efficacious therapeutic approaches.In this comprehensive review we will discuss the state-of-the-art knowledge about the epigenetic landscape in hepatocarcinogenesis, including evidence on the diagnostic and prognostic role of non-coding RNAs, modifications occurring at the chromatin level, and their role in the era of precision medicine.Apart from other better-known risk factors that predispose to the development of HCC, characterization of the epigenetic remodelling that occurs during hepatocarcinogenesis could open the way to the identification of personalized biomarkers. It may also enable a more accurate diagnosis and stratification of patients, and the discovery of new targets for more efficient therapeutic approaches.

摘要

肝细胞癌(HCC)是最常见的原发性肝癌,是第六种最常见的癌症诊断,也是癌症相关死亡的第四大原因。与其他异质性实体瘤一样,HCC 是遗传改变与表观遗传修饰混合的独特协同组合的结果。在 HCC 中,体细胞变异的模式和频率取决于附近的染色质。另一方面,表观遗传改变通常会导致易发生突变的基因组不稳定性。表观遗传学是指基因表达的可遗传状态,而不改变 DNA 序列本身,与遗传变化不同,表观遗传修饰是可逆的,并且比遗传变化更广泛地影响基因表达。因此,对表观遗传调控及其涉及的分子机制的研究极大地有助于理解 HCC 发病机制和异质性的机制。此外,这方面的知识有助于识别 HCC 诊断和预后的生物标志物,以及未来更有效的治疗方法的新靶点。在这篇全面的综述中,我们将讨论肝癌发生过程中表观遗传学景观的最新知识,包括非编码 RNA 的诊断和预后作用、染色质水平发生的修饰及其在精准医学时代的作用的证据。除了其他导致 HCC 发生的已知风险因素外,对肝癌发生过程中表观遗传重塑的特征描述可能为识别个体化生物标志物开辟道路。它还可能实现更准确的诊断和患者分层,并发现更有效的治疗方法的新靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93c0/8943959/6a1d25d13b19/13046_2022_2297_Fig1_HTML.jpg

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