AI Article Synopsis

  • The Wnt/β-catenin pathway is often overactive in lung cancer, promoting tumor growth and resistance to treatment, which contributes to higher disease rates and severe outcomes.
  • Despite its potential as a target for therapy, challenges like tumor diversity and pathway complexity complicate effective treatment development.
  • This study reviews various natural products and compounds that inhibit the Wnt/β-catenin pathway, highlighting their promising anticancer effects and lower toxicity, suggesting their potential for safer, more efficient lung cancer therapies.

Article Abstract

The Wnt/β-catenin pathway is abnormally activated in most lung cancer tissues and considered to be an accelerator of carcinogenesis and lung cancer progression, which is closely related to increased morbidity rates, malignant progression, and treatment resistance. Although targeting the canonical Wnt/β-catenin pathway shows significant potential for lung cancer therapy, it still faces challenges owing to its complexity, tumor heterogeneity and wide physiological activity. Therefore, it is necessary to elucidate the role of the abnormal activation of the Wnt/β-catenin pathway in lung cancer progression. Moreover, Wnt inhibitors used in lung cancer clinical trials are expected to break existing therapeutic patterns, although their adverse effects limit the treatment window. This is the first study to summarize the research progress on various compounds, including natural products and derivatives, that target the canonical Wnt pathway in lung cancer to develop safer and more targeted drugs or alternatives. Various natural products have been found to inhibit Wnt/β-catenin in various ways, such as through upstream and downstream intervention pathways, and have shown encouraging preclinical anti-tumor efficacy. Their diversity and low toxicity make them a popular research topic, laying the foundation for further combination therapies and drug development.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10568034PMC
http://dx.doi.org/10.3389/fphar.2023.1250893DOI Listing

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