Collagen prolyl 4-hydroxylase 1 is essential for HIF-1α stabilization and TNBC chemoresistance

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作者
Gaofeng Xiong
Rachel L. Stewart
Jie Chen
Tianyan Gao
Timothy L. Scott
Luis M. Samayoa
Kathleen O’Connor
Andrew N. Lane
Ren Xu
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[1] University of Kentucky,UK Markey Cancer Center
[2] University of Kentucky,Department of Pharmacology and Nutritional Sciences
[3] University of Kentucky,Department of Pathology and Laboratory Medicine
[4] University of Kentucky,Department of Molecular and Cellular Biochemistry
[5] University of Kentucky,Center for Environmental and Systems Biochemistry
[6] University of Kentucky,Department of Toxicology and Cancer Biology
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Collagen prolyl 4-hydroxylase (P4H) expression and collagen hydroxylation in cancer cells are necessary for breast cancer progression. Here, we show that P4H alpha 1 subunit (P4HA1) protein expression is induced in triple-negative breast cancer (TNBC) and HER2 positive breast cancer. By modulating alpha ketoglutarate (α-KG) and succinate levels P4HA1 expression reduces proline hydroxylation on hypoxia-inducible factor (HIF) 1α, enhancing its stability in cancer cells. Activation of the P4HA/HIF-1 axis enhances cancer cell stemness, accompanied by decreased oxidative phosphorylation and reactive oxygen species (ROS) levels. Inhibition of P4HA1 sensitizes TNBC to the chemotherapeutic agent docetaxel and doxorubicin in xenografts and patient-derived models. We also show that increased P4HA1 expression correlates with short relapse-free survival in TNBC patients who received chemotherapy. These results suggest that P4HA1 promotes chemoresistance by modulating HIF-1-dependent cancer cell stemness. Targeting collagen P4H is a promising strategy to inhibit tumor progression and sensitize TNBC to chemotherapeutic agents.
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