作为肝细胞癌新病因的 MASH:当前知识和未来展望。

IF 6.6 2区 医学 Q1 Biochemistry, Genetics and Molecular Biology Molecular Oncology Pub Date : 2025-02-01 Epub Date: 2024-06-14 DOI:10.1002/1878-0261.13685
Michael Karin, Ju Youn Kim
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引用次数: 0

摘要

肝细胞癌是致死率最高、增长速度最快的癌症之一。在 HCC 病因中,代谢功能障碍相关性脂肪肝(MAFLD)是导致 HCC 的主要因素,因为它极有可能加重肝硬化。肥胖环境会促进正能量平衡,导致肥胖和代谢综合征持续上升。然而,目前还很难了解代谢并发症如何导致肝病的不良预后,以及哪些分子机制是 MAFLD 驱动 HCC 发展的基础。因此,需要建立能再现人类病因的合适临床前模型。目前已建立了许多临床前模型,但能模拟患者人体测量指标和疾病进展过程的临床前模型并不多。在此,我们回顾了有关脂肪组织、肝脏相关 HCC 病因以及最近在 MAFLD 驱动的 HCC 患者中发现的基因突变特征的文献。我们还对目前建议用于 MAFLD 驱动的 HCC 研究的啮齿动物模型进行了批判性回顾。
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MASH as an emerging cause of hepatocellular carcinoma: current knowledge and future perspectives.

Hepatocellular carcinoma is one of the deadliest and fastest-growing cancers. Among HCC etiologies, metabolic dysfunction-associated fatty liver disease (MAFLD) has served as a major HCC driver due to its great potential for increasing cirrhosis. The obesogenic environment fosters a positive energy balance and results in a continuous rise of obesity and metabolic syndrome. However, it is difficult to understand how metabolic complications lead to the poor prognosis of liver diseases and which molecular mechanisms are underpinning MAFLD-driven HCC development. Thus, suitable preclinical models that recapitulate human etiologies are essentially required. Numerous preclinical models have been created but not many mimicked anthropometric measures and the course of disease progression shown in the patients. Here we review the literature on adipose tissues, liver-related HCC etiologies and recently discovered genetic mutation signatures found in MAFLD-driven HCC patients. We also critically review current rodent models suggested for MAFLD-driven HCC study.

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来源期刊
Molecular Oncology
Molecular Oncology Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
11.80
自引率
1.50%
发文量
203
审稿时长
10 weeks
期刊介绍: Molecular Oncology highlights new discoveries, approaches, and technical developments, in basic, clinical and discovery-driven translational cancer research. It publishes research articles, reviews (by invitation only), and timely science policy articles. The journal is now fully Open Access with all articles published over the past 10 years freely available.
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