Hepatocellular carcinoma (HCC) is one of the deadliest cancers globally, with increasing incidence and mortality rates.

It arises from chronic liver diseases, including hepatitis B or C infections, alcohol consumption, and metabolic disorders, often leading to liver cirrhosis.

However, early detection is challenging as HCC is typically asymptomatic until advanced stages, limiting treatment options.

While chemotherapy, immunotherapy, and targeted therapies are employed, their efficacy remains suboptimal.

Thus, understanding the molecular mechanisms driving HCC is essential for developing new therapeutic strategies.

A growing body of research highlights the crucial role of the Wnt signalling pathway, especially its β-catenin axis, in HCC.

This pathway regulates essential processes such as cell proliferation, migration, and immune evasion.

This article reviews the involvement of the Wnt signalling pathway in HCC, its underlying mechanisms, and its potential as a therapeutic target.

Wnt Signalling Pathway

The Wnt signalling pathway is a conserved network that regulates cell proliferation, differentiation, and migration.

It consists of the canonical Wnt/β-catenin pathway and non-canonical pathways such as Wnt/PCP and Wnt/Ca2+.

In the canonical pathway, Wnt ligands bind to Frizzled receptors, stabilising β-catenin, which accumulates in the cytoplasm and enters the nucleus.

In the nucleus, β-catenin activates downstream genes like c-Myc and Cyclin D1, promoting cell proliferation and survival.

In HCC, mutations in key components of the Wnt pathway, including β-catenin (encoded by CTNNB1), AXIN, and APC, lead to sustained activation of this pathway.

This dysregulation drives HCC progression by enhancing cell proliferation, migration, and immune evasion.

Furthermore, extracellular vesicles (EVs) have been found to modulate Wnt signalling by delivering Wnt ligands and miRNAs, influencing tumour progression and immune response.

Molecular Mechanisms in HCC

Mutations in the CTNNB1 gene, which encodes β-catenin, lead to its stabilisation and nuclear translocation, activating Wnt target genes and driving tumour growth.

Additionally, mutations in AXIN and APC, which regulate β-catenin degradation, further enhance Wnt/β-catenin signalling.

Research also reveals that EVs play a significant role in modulating this pathway.

EVs can carry Wnt ligands, such as Wnt3a and Wnt5a, which bind to Frizzled receptors on recipient cells, further promoting tumour proliferation and metastasis.

They also transport miRNAs that affect the Wnt signalling components, influencing tumour behaviour.

Role of Wnt Signalling in HCC Pathogenesis

The Wnt/β-catenin pathway is essential for HCC development.

Its activation promotes hepatocyte proliferation, inhibits apoptosis, and enhances tumour cell migration and invasion.

β-catenin accumulation in the nucleus activates genes involved in cell cycle progression and survival, including c-Myc and Cyclin D1.

Additionally, β-catenin inhibits pro-apoptotic genes like Bax and Bim, further supporting tumour cell survival.

The Wnt pathway also plays a role in epithelial-mesenchymal transition (EMT), which enables epithelial cells to acquire mesenchymal characteristics such as enhanced motility and invasiveness.

This transition, regulated by Wnt signalling, promotes tumour cell migration, invasion, and metastasis.

Additionally, the pathway influences angiogenesis by increasing the expression of vascular endothelial growth factor (VEGF), which supports tumour blood supply and further enhances metastatic potential.

Therapeutic Implications

Given the pivotal role of the Wnt/β-catenin pathway in HCC, targeting this signalling cascade holds significant promise.

Several therapeutic strategies are being explored, including small molecule inhibitors, monoclonal antibodies, and gene therapies.

β-catenin inhibitors, such as GSK-3β inhibitors, work by preventing β-catenin's nuclear translocation, thus inhibiting the activation of downstream genes involved in proliferation and survival.

Wnt competitive inhibitors, which block the binding of Wnt ligands to Frizzled receptors, also show promise in reducing Wnt pathway activation and inhibiting HCC growth.

Clinical trials are underway to evaluate the safety and efficacy of these therapies.

In addition, combination therapies targeting both the Wnt pathway and other aspects of the tumour microenvironment, such as immune checkpoint inhibitors or anti-angiogenic agents, may enhance therapeutic efficacy.

Conclusion

The Wnt/β-catenin pathway plays a central role in HCC initiation, progression, and metastasis.

Mutations in β-catenin and other components like AXIN and APC lead to aberrant activation of this pathway, driving tumour growth and immune evasion.

Targeting Wnt signalling offers a promising therapeutic strategy for HCC.

Several inhibitors targeting β-catenin, Frizzled receptors, and other downstream components are currently being evaluated in clinical trials.

Despite challenges such as pathway complexity and drug resistance, Wnt-targeted therapies, especially when combined with other treatments, hold potential for improving HCC treatment outcomes.

The study was published in the Journal of Clinical and Translational Hepatology.

Source: Xia & He Publishing Inc.