Targeting HIF-1 for prostate cancer: a synthesis of preclinical evidence

Yarden Zohar, Nicola J. Mabjeesh

    Research output: Contribution to journalReview articlepeer-review

    4 Scopus citations

    Abstract

    Introduction: Hypoxia-inducible factor (HIF) mediates multiple intracellular processes that drive cellular metabolism and induce proliferation. Dysregulated HIF expression is associated with oncogenic cellular transformation. Moreover, high HIF levels correlate with tumor aggressiveness and chemoresistance, indicating the vital effect of HIF-1α on tumorigenicity. Currently, widespread in-vitro and in-vivo research is focusing on targeting HIF with drugs that have already been approved for use by the FDA, such as belzutifan, in renal cell carcinoma. HIF inhibition is mostly associated with tumor size reduction; however, drug toxicity remains a challenge. Area covered: In this review, we focus on the potential of targeting HIF in prostate cancer (PC) and summarize the scientific background of HIF activity in PC. This finding emphasizes the rationale for using HIF as a therapeutic target in this malignancy. We have listed known HIF inhibitors that are being investigated in preclinical studies and their potential as anticancer drugs for PC. Expert opinion: Although HIF-targeting agents have been investigated for over a decade, their use in therapy-resistant cancers remains relevant and should be explored further. In addition, the use of naturally occurring HIF inhibitors should be considered as an add-on therapy for the currently used regimens.

    Original languageEnglish
    Pages (from-to)715-731
    Number of pages17
    JournalExpert Opinion on Therapeutic Targets
    Volume27
    Issue number8
    DOIs
    StatePublished - 1 Jan 2023

    Keywords

    • Androgen receptor
    • HIF
    • castration-resistant
    • hypoxia-inducible factor
    • preclinical studies
    • prostate adenocarcinoma
    • prostate cancer

    ASJC Scopus subject areas

    • Molecular Medicine
    • Pharmacology
    • Drug Discovery
    • Clinical Biochemistry

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