Hepatocellular carcinoma: signaling pathways and therapeutic advances
Гепатоцеллюлярная карцинома: сигнальные пути и терапевтические достижения
2025-02-06
SCID: 54.1/wn6ct5ar
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anti-VEGF therapyhepatocellular carcinomaimmune checkpoint inhibitors (ICI)receptor tyrosine kinase (RTK) pathwaystyrosine kinase inhibitors (TKI)
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Abstract (AI)
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.
Key Findings
1
Current primary therapies for advanced HCC are tyrosine kinase inhibitors (TKIs), immune checkpoint inhibitors (ICIs), and combination regimens; ongoing trials combine ICIs with TKIs, anti-VEGF therapies, or dual immunotherapies.
2
Early-stage HCC is often asymptomatic, causing delayed diagnosis and frequent presentation at advanced, largely incurable stages.
3
Hepatocellular carcinoma (HCC) accounts for ~90% of liver cancer and is linked to aflatoxin, HBV, HCV, and metabolic disorders, with rising incidence expected to exceed 1 million new cases annually by 2025.
4
Investigating signaling pathways, their inhibitors, biomarkers, and results from late-stage clinical trials is pivotal to develop more effective HCC therapeutics and could revolutionize management across disease stages.
5
Multiple dysregulated signaling pathways beyond RTKs (including pathways for cell differentiation, telomere regulation, epigenetic modification, and stress response) contribute to HCC progression and represent therapeutic targets.
Research Object
Hepatocellular carcinoma (HCC)
Research Subject
Dysregulated cellular signaling pathways in HCC and their therapeutic targeting, including RTK pathways, pathways regulating differentiation, telomeres, epigenetic modification and stress response, and clinical efficacy of TKIs, ICIs and combination regimens
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2025-02-06
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