β-catenin at the crossroads of cancer and neurodevelopment

Caroline E Nunes-Xavier1, Ana Rodríguez-Ramos2, Rafael Pulido3

  • 1Biobizkaia Health Research Institute, Barakaldo, Spain; CIBERER, ISCIII, Madrid, Spain; Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.

Trends in Cancer
|May 29, 2026
PubMed

Insights

Beta-catenin (CTNNB1) is crucial for cell development and has therapeutic potential for cancer and neurodevelopmental disorders. Understanding its opposing roles in disease is key to developing effective CTNNB1-based therapies.

Area of Science:

  • Molecular Biology
  • Cell Biology
  • Developmental Biology

Background:

  • Beta-catenin (CTNNB1) plays a fundamental role in cellular development and tissue homeostasis.
  • Dysregulation of CTNNB1 is implicated in various pathologies, including cancer and neurodevelopmental syndromes.
  • Altered CTNNB1 function in different diseases necessitates distinct therapeutic strategies.

Purpose of the Study:

  • To elucidate the dual role of beta-catenin (CTNNB1) in both normal development and disease states.
  • To highlight the therapeutic potential of targeting CTNNB1 in oncology and neurology.
  • To emphasize the need for a comprehensive understanding of CTNNB1's physiological and pathological functions.

Main Methods:

  • Literature review and synthesis of existing research on CTNNB1.
  • Analysis of genetic alterations in CTNNB1 associated with specific diseases.
  • Comparative study of beta-catenin function in cancer versus neurodevelopmental disorders.

Main Results:

  • Beta-catenin's function is context-dependent, with opposing alterations in cancer and neurodevelopmental syndromes.
  • Distinct genetic events in CTNNB1 lead to divergent pathological outcomes.
  • Therapeutic approaches for CTNNB1-related diseases are often antagonistic.

Conclusions:

  • A thorough understanding of beta-catenin (CTNNB1) biology is essential for advancing therapeutic interventions.
  • Targeting CTNNB1 offers promising avenues for treating cancer and neurodevelopmental disorders.
  • Future research should focus on dissecting the specific mechanisms underlying CTNNB1 dysregulation in different pathologies.

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