Pathogenesis to management of hepatocellular carcinoma.

Q2 Biochemistry, Genetics and Molecular Biology
Ben L Da, Kelly I Suchman, Lawrence Lau, Atoosa Rabiee, Aiwu Ruth He, Kirti Shetty, Herbert Yu, Linda L Wong, Richard L Amdur, James M Crawford, Sharon S Fox, Gregory M Grimaldi, Priya K Shah, Jonathan Weinstein, David Bernstein, Sanjaya K Satapathy, Nyasha Chambwe, Xiyan Xiang, Lopa Mishra
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引用次数: 1

Abstract

Hepatocellular carcinoma (HCC) is the most common primary liver cancer whose incidence continues to rise in many parts of the world due to a concomitant rise in many associated risk factors, such as alcohol use and obesity. Although early-stage HCC can be potentially curable through liver resection, liver-directed therapies, or transplantation, patients usually present with intermediate to advanced disease, which continues to be associated with a poor prognosis. This is because HCC is a cancer with significant complexities, including substantial clinical, histopathologic, and genomic heterogeneity. However, the scientific community has made a major effort to better characterize HCC in those aspects via utilizing tissue sampling and histological classification, whole genome sequencing, and developing viable animal models. These efforts ultimately aim to develop clinically relevant biomarkers and discover molecular targets for new therapies. For example, until recently, there was only one approved systemic therapy for advanced or metastatic HCC in the form of sorafenib. Through these efforts, several additional targeted therapies have gained approval in the United States, although much progress remains to be desired. This review will focus on the link between characterizing the pathogenesis of HCC with current and future HCC management.

Abstract Image

Abstract Image

Abstract Image

肝细胞癌的发病机制与治疗。
肝细胞癌(HCC)是最常见的原发性肝癌,由于饮酒和肥胖等相关危险因素的增加,其发病率在世界许多地区持续上升。尽管早期HCC可以通过肝切除、肝定向治疗或移植治愈,但患者通常表现为中晚期疾病,这仍然与预后不良相关。这是因为HCC是一种非常复杂的癌症,包括大量的临床、组织病理学和基因组异质性。然而,科学界已经通过利用组织取样和组织学分类、全基因组测序和开发可行的动物模型,在这些方面做出了重大努力来更好地表征HCC。这些努力的最终目标是开发临床相关的生物标志物,并发现新疗法的分子靶点。例如,直到最近,只有一种以索拉非尼的形式被批准用于晚期或转移性HCC的全身治疗。通过这些努力,一些额外的靶向治疗已在美国获得批准,尽管仍需取得很大进展。本文将重点讨论HCC的发病机制特征与当前和未来HCC治疗之间的联系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Genes and Cancer
Genes and Cancer Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.90
自引率
0.00%
发文量
6
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