Wingless/It/β-catenin signaling in liver metastasis from colorectal cancer: A focus on biological mechanisms and therapeutic opportunities

World J Gastroenterol. 2023 May 14;29(18):2764-2783. doi: 10.3748/wjg.v29.i18.2764.

Abstract

The liver is the most common site of metastases in patients with colorectal cancer. Colorectal liver metastases (CRLMs) are the result of molecular mechanisms that involve different cells of the liver microenvironment. The aberrant activation of Wingless/It (Wnt)/β-catenin signals downstream of Wnt ligands initially drives the oncogenic transformation of the colon epithelium, but also the progression of metastatization through the epithelial-mesenchymal transition/mesenchymal-epithelial transition interactions. In liver microenvironment, metastatic cells can also survive and adapt through dormancy, which makes them less susceptible to pro-apoptotic signals and therapies. Treatment of CRLMs is challenging due to its variability and heterogeneity. Advances in surgery and oncology have been made in the last decade and a pivotal role for Wnt/β-catenin pathway has been re-cognized in chemoresistance. At the state of art, there is a lack of clear understanding of why and how this occurs and thus where exactly the opportunities for developing anti-CRLMs therapies may lie. In this review, current knowledge on the involvement of Wnt signaling in the development of CRLMs was considered. In addition, an overview of useful biomarkers with a revision of surgical and non-surgical therapies currently accepted in the clinical practice for colorectal liver metastasis patients were provided.

Keywords: Colorectal cancer; Epithelial-mesenchymal transition/ mesenchymal-epithelial transition; Liver metastasis; Markers; Surgical and non-surgical therapies; Wingless/It/β-catenin signaling.

Publication types

  • Review

MeSH terms

  • Cell Line, Tumor
  • Cell Movement
  • Colorectal Neoplasms* / genetics
  • Epithelial-Mesenchymal Transition
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Liver Neoplasms* / genetics
  • Neoplasm Metastasis
  • Tumor Microenvironment
  • Wnt Signaling Pathway
  • beta Catenin / metabolism

Substances

  • beta Catenin