Hepatocellular carcinoma: signaling pathways and therapeutic advances

肝细胞癌 医学 癌症研究 转移 免疫疗法 癌症 信号转导 酪氨酸激酶 生物信息学 肿瘤科 内科学 生物 受体 生物化学
作者
Jiaojiao Zheng,Siying Wang,Lei Xia,Sun Zhen,Kui Ming Chan,René Bernards,Wenxin Qin,Jinhong Chen,Qiang Xia,Haojie Jin
出处
期刊:Signal Transduction and Targeted Therapy [Springer Nature]
卷期号:10 (1): 35-35 被引量:303
标识
DOI:10.1038/s41392-024-02075-w
摘要

Liver cancer represents a major global health concern, with projections indicating that the number of new cases could surpass 1 million annually by 2025. Hepatocellular carcinoma (HCC) constitutes around 90% of liver cancer cases and is primarily linked to factors incluidng aflatoxin, hepatitis B (HBV) and C (HCV), and metabolic disorders. There are no obvious symptoms in the early stage of HCC, which often leads to delays in diagnosis. Therefore, HCC patients usually present with tumors in advanced and incurable stages. Several signaling pathways are dis-regulated in HCC and cause uncontrolled cell propagation, metastasis, and recurrence of HCC. Beyond the frequently altered and therapeutically targeted receptor tyrosine kinase (RTK) pathways in HCC, pathways involved in cell differentiation, telomere regulation, epigenetic modification and stress response also provide therapeutic potential. Investigating the key signaling pathways and their inhibitors is pivotal for achieving therapeutic advancements in the management of HCC. At present, the primary therapeutic approaches for advanced HCC are tyrosine kinase inhibitors (TKI), immune checkpoint inhibitors (ICI), and combination regimens. New trials are investigating combination therapies involving ICIs and TKIs or anti-VEGF (endothelial growth factor) therapies, as well as combinations of two immunotherapy regimens. The outcomes of these trials are expected to revolutionize HCC management across all stages. Here, we provide here a comprehensive review of cellular signaling pathways, their therapeutic potential, evidence derived from late-stage clinical trials in HCC and discuss the concepts underlying earlier clinical trials, biomarker identification, and the development of more effective therapeutics for HCC.
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