ArticleCell death & disease2026
HIF1 inhibition targets tumoral and myeloid cells, and is a promising therapy for metastatic castration-resistant prostate cancer.
Article in Cell death & disease, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Metastatic prostate cancer (PCa) remains lethal due to limited effective therapies. PTEN and TP53 are commonly mutated tumor suppressors in metastatic PCa, yet the molecular and cellular mechanisms driving aggressiveness and treatment resistance are not fully understood. We have previously shown that mice with both Pten and Trp53 inactivation in prostate luminal cells at adulthood develop aggressive intraductal prostate carcinoma (IDC) and liver metastases. By combining single-cell and spatial transcriptomics, along with flow cytometry and immunohistochemical analyses, we now reveal that prostatic tumors of such mice are hypoxic and progress within a complex immune microenvironment, including neutrophils, TREM2⁺ macrophages, and CCR2⁺ myeloid cells. Moreover, we uncovered that genetic Hif1a inactivation in prostate luminal cells or pharmacological inhibition of HIF1 signaling in Pten/Trp53
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