Regulation of elevated expression of Mcl-1 in hepatocellular carcinoma - a review.

IF 2.6 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Li Chen, Yuwei He, Xudong Jiang, Audrey Siew Foong Kow, Yu Zhao Lee, Chau Ling Tham, Rohana Yusof, Ming Tatt Lee
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引用次数: 0

Abstract

Hepatocellular carcinoma (HCC) is one of the most prevalent malignant tumors worldwide. Mcl-1 (myeloid cell leukemia-1) is highly expressed in HCC cells and plays a critical role in chemotherapy resistance and is a major contributor to chemotherapy failure in HCC. The purpose of this study is to review the recent research progress that explores the key factors in regulating Mcl-1 overexpression in HCC cells, contributing to chemotherapy resistance. The related studies from the past decade on agents targeting Mcl-1 to inhibit HCC were also reviewed to provide insights into overcoming chemotherapy resistance in HCC. Mcl-1 overexpression in HCC is mainly regulated by transcription factors (such as STAT3, p53), non-coding RNAs (such as miRNA, lncRNA), cell cycle proteins, mitochondrial dynamics, and the hypoxic microenvironment. Targeting Mcl-1, alongside multi-target combination therapies, may overcome HCC chemotherapy resistance and improve outcomes. Future research should focus on strategies addressing multiple pathways to minimize monotherapy resistance risks and offer enhanced treatment options for the betterment of human health.

Mcl-1在肝细胞癌中的表达调控研究进展
肝细胞癌(HCC)是世界上最常见的恶性肿瘤之一。Mcl-1(髓样细胞白血病-1)在HCC细胞中高表达,在化疗耐药中起关键作用,是HCC化疗失败的主要因素。本研究旨在综述近年来肝癌细胞中Mcl-1过表达调控及化疗耐药的关键因素的研究进展。回顾了近十年来针对Mcl-1抑制HCC药物的相关研究,为克服HCC的化疗耐药提供见解。Mcl-1在HCC中的过表达主要受转录因子(如STAT3、p53)、非编码rna(如miRNA、lncRNA)、细胞周期蛋白、线粒体动力学、缺氧微环境等因素的调控。靶向Mcl-1与多靶点联合治疗可能克服HCC化疗耐药并改善预后。未来的研究应侧重于解决多种途径的策略,以尽量减少单药耐药风险,并为改善人类健康提供更好的治疗选择。
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来源期刊
Journal of Receptors and Signal Transduction
Journal of Receptors and Signal Transduction 生物-生化与分子生物学
CiteScore
6.60
自引率
0.00%
发文量
19
审稿时长
>12 weeks
期刊介绍: Journal of Receptors and Signal Tranduction is included in the following abstracting and indexing services: BIOBASE; Biochemistry and Biophysics Citation Index; Biological Abstracts; BIOSIS Full Coverage Shared; BIOSIS Previews; Biotechnology Abstracts; Current Contents/Life Sciences; Derwent Chimera; Derwent Drug File; EMBASE; EMBIOLOGY; Journal Citation Reports/ Science Edition; PubMed/MedLine; Science Citation Index; SciSearch; SCOPUS; SIIC.
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