Non-alcoholic fatty liver disease and diabetes mellitus as growing aetiologies of hepatocellular carcinoma

被引:24
|
作者
Talamantes, Stephanie [1 ]
Lisjak, Michela [1 ]
Gilglioni, Eduardo H. [1 ]
Llamoza-Torres, Camilo J. [2 ]
Ramos-Molina, Bruno [3 ]
Gurzov, Esteban N. [1 ,3 ,4 ,5 ]
机构
[1] Univ Libre Bruxelles, Signal Transduct & Metab Lab, Lab Gastroenterol Expt & Endotools, Route Lennik 808, B-1070 Brussels, Belgium
[2] Virgen de la Arrixaca Univ Hosp, Dept Hepatol, Murcia 30120, Spain
[3] Biomed Res Inst Murcia IMIB, Obes & Metab Lab, Murcia 30120, Spain
[4] WEL Res Inst, WELBIO Dept, Ave Pasteur 6, B-1300 Wavre, Belgium
[5] Signal Transduct & Metab Lab, Route Lennik 808, B-1070 Brussels, Belgium
基金
欧洲研究理事会;
关键词
Hepatocellular carcinoma; obesity; non-alcoholic fatty liver disease; type; 2; diabetes; hepatocyte transformation; HEPATIC OXIDATIVE STRESS; NF-KAPPA-B; INSULIN-RESISTANCE; REDUCED RISK; SORAFENIB TREATMENT; LIPID-METABOLISM; DNA METHYLATION; ACID SYNTHASE; DOUBLE-BLIND; METFORMIN;
D O I
10.1016/j.jhepr.2023.100811
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Obesity-related complications such as non-alcoholic fatty liver disease (NAFLD) and type 2 diabetes (T2D) are well-established risk factors for the development of hepatocellular carcinoma (HCC). This review provides insights into the molecular mechanisms that underlie the role of steatosis, hyperinsulinemia and hepatic inflammation in HCC development and progression. We focus on recent findings linking intracellular pathways and transcription factors that can trigger the reprogramming of hepatic cells. In addition, we highlight the role of enzymes in dysregulated metabolic activity and consequent dysfunctional signalling. Finally, we discuss the potential uses and challenges of novel therapeutic strategies to prevent and treat NAFLD/T2D-associated HCC. & COPY; 2023 The Author(s). Published by Elsevier B.V. on behalf of European Association for the Study of the Liver (EASL). This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/ licenses/by-nc-nd/4.0/).
引用
收藏
页数:19
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