Exploring the Wnt pathway as a therapeutic target for prostate cancer

Helen B. Pearson, Sarah Koushyar, Valerie S. Meniel, Toby J. Phesse

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    Abstract

    Aberrant activation of the Wnt pathway is emerging as a frequent event during prostate cancer that can facilitate tumor formation, progression, and therapeutic resistance. Recent discoveries indicate that targeting the Wnt pathway to treat prostate cancer may be efficacious. However, the functional consequence of activating the Wnt pathway during the different stages of prostate cancer progression remains unclear. Preclinical work investigating the efficacy of targeting Wnt signaling for the treatment of prostate cancer, both in primary and metastatic lesions, and improving our molecular understanding of treatment responses is crucial to identifying effective treatment strategies and biomarkers that help guide treatment decisions and improve patient care. In this review, we outline the type of genetic alterations that lead to activated Wnt signaling in prostate cancer, highlight the range of laboratory models used to study the role of Wnt genetic drivers in prostate cancer, and discuss new mechanistic insights into how the Wnt cascade facilitates prostate cancer growth, metastasis, and drug resistance.
    Original languageEnglish
    Article number309
    JournalBiomolecules
    Volume12
    Issue number2
    Early online date15 Feb 2022
    DOIs
    Publication statusPublished - 28 Feb 2022

    Bibliographical note

    Note: This work was supported by Prostate Cancer Research in the United Kingdom, grant reference 6962 (awarded to T.J.P. and H.B.P.), Medical Research Council (MR/R026424/1 to T.J.P.), BLS Fellowship (T.J.P.) H.B.P. is supported by a Cancer Research UK career development fellowship (A27894).

    Keywords

    • APC
    • Biological sciences
    • CRPC
    • Wnt
    • metastasis
    • prostate cancer
    • targeted therapy
    • ╬▓-catenin

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