Park Hyunjung, Park Hyerin, Baek Jiyeon, Moon Hyuk, Ro Simon Weonsang
Department of Genetics and Biotechnology, College of Life Sciences, Kyung Hee University, Yongin-si 17104, Korea.
Biology (Basel). 2022 Apr 12;11(4):585. doi: 10.3390/biology11040585.
Hepatocellular carcinoma (HCC) is a major health concern worldwide, and its incidence is increasing steadily. To date, receptor tyrosine kinases (RTKs) are the most favored molecular targets for the treatment of HCC, followed by immune checkpoint regulators such as PD-1, PD-L1, and CTLA-4. With less than desirable clinical outcomes from RTK inhibitors as well as immune checkpoint inhibitors (ICI) so far, novel molecular target therapies have been proposed for HCC. In this review, we will introduce diverse molecular signaling pathways that are aberrantly activated in HCC, focusing on YAP/TAZ, Hedgehog, and Wnt/β-catenin signaling pathways, and discuss potential therapeutic strategies targeting the signaling pathways in HCC.
肝细胞癌(HCC)是全球主要的健康问题,其发病率正在稳步上升。迄今为止,受体酪氨酸激酶(RTK)是治疗HCC最受青睐的分子靶点,其次是免疫检查点调节剂,如PD-1、PD-L1和CTLA-4。由于目前RTK抑制剂以及免疫检查点抑制剂(ICI)的临床疗效不尽人意,因此已提出针对HCC的新型分子靶向疗法。在本综述中,我们将介绍在HCC中异常激活的多种分子信号通路,重点关注YAP/TAZ、Hedgehog和Wnt/β-连环蛋白信号通路,并讨论针对HCC中这些信号通路的潜在治疗策略。