Clinically approved HIF-PHIs modulate redox metabolism, cell growth, and angiogenesis independent of HIF-1α/HIF-2α

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Authors: Daniela Mennerich, Fawzi Khoder‐Agha, Mustafa Beter, Elitsa Y. Dimova, Seppo Ylä-Herttuala, Thomas Kietzmann
Cited by: 1
References: 71

Abstract

HIF-prolyl hydroxylase inhibitors are used to treat anemia in chronic kidney disease. These drugs stabilize hypoxia-inducible factors HIF-1α and HIF-2α, which activate erythropoiesis and iron metabolism pathways. Clinically approved HIF-PHIs including roxadustat and molidustat exhibit distinct molecular structures and selectivity profiles, yet their HIF-independent effects remain poorly understood. Here we show that roxadustat and molidustat modulate mitochondrial function, oxidative stress, lysosomal activity, and lipid accumulation, resulting in distinct cellular phenotypes in HIF-null cells. Notably, roxadustat exhibited anti-proliferative and anti-angiogenic activity in HIF-null cells, contradicting expectations of VEGF-driven angiogenesis via HIF stabilization. RNA sequencing and pathway analysis revealed compound-specific off-target gene regulation affecting cellular processes beyond canonical hypoxia responses including energy metabolism and immune signaling. These findings illuminate mechanisms underlying potential adverse effects-such as thrombosis- and identify alternative therapeutic pathways, providing a framework for optimizing HIF-PHI safety profiles and expanding their clinical applications in oncology and metabolic disorders.

Fields of Study & Subjects

Cancer Hypoxia and Metabolism Erythropoietin and Anemia Treatment Histone Deacetylase Inhibitors Research

Publication details

Journal / source
Redox Biology
Publisher
Elsevier BV
Volume
94
Pages
104206–104206
Publication date
14 May 2026
Language
EN