Targeting of HIF2-driven cachexia in kidney cancer

Kidney cancer frequently causes paraneoplastic syndromes, including hypercalcemia and cachexia, but the underlying mechanisms are incompletely understood. The most common form of kidney cancer, clear cell renal cell carcinoma (ccRCC), is frequently caused by loss of the pVHL tumor suppressor protein and the resulting upregulation of the HIF2 transcription factor. We show that PTHLH, which resides on a ccRCC amplicon on chromosome 12p, is a direct HIF2 transcriptional target in ccRCC. Further, we show that the increased PTHLH expression is both necessary and sufficient for the induction of hypercalcemia and cachexia in preclinical orthotopic cell line tumor models. Consistent with these observations, two different allosteric HIF2 inhibitors, belzutifan and NKT2152, rapidly ameliorated hypercalcemia and cachexia in patients with ccRCC, including in some who did not exhibit objective tumor shrinkage. Our findings support prospective clinical studies to determine whether HIF2 inhibitors can be leveraged not only for tumor control, but also for the treatment of cancer-associated cachexia in renal cell carcinoma.

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Publication Details

Journal
Nature Medicine
Published
2025-11-28
DOI
https://doi.org/10.1038/s41591-025-04054-2
Citations
3
Primary Topic
Cancer, Hypoxia, and Metabolism
Type
article
Field-Weighted Citation Impact
2.81
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article

Targeting of HIF2-driven cachexia in kidney cancer

Jing Lu, Eddy Saad, Kei Enomoto, Laura Stransky et al.
3 citations
Nature Medicine
Cancer, Hypoxia, and Metabolism
2.81
article

Targeting of HIF2-driven cachexia in kidney cancer

Jing Lu, Eddy Saad, Kei Enomoto, Laura Stransky, Namrata D. Udeshi, Hairong Wei, Muhannad Abu‐Remaileh, Nikita Bhalerao, Steven A. Carr, Hilina Woldemichael, Toni K. Choueiri, Sean M. Vigeant, Jason R. Pitarresi, Nitin H. Shirole, Marc Machaalani, Qinqin Jiang, Chunbao Charles Xu, William G. Kaelin, William Sun, Zhihong Liu
article en
3 citations

Abstract

Kidney cancer frequently causes paraneoplastic syndromes, including hypercalcemia and cachexia, but the underlying mechanisms are incompletely understood. The most common form of kidney cancer, clear cell renal cell carcinoma (ccRCC), is frequently caused by loss of the pVHL tumor suppressor protein and the resulting upregulation of the HIF2 transcription factor. We show that PTHLH, which resides on a ccRCC amplicon on chromosome 12p, is a direct HIF2 transcriptional target in ccRCC. Further, we show that the increased PTHLH expression is both necessary and sufficient for the induction of hypercalcemia and cachexia in preclinical orthotopic cell line tumor models. Consistent with these observations, two different allosteric HIF2 inhibitors, belzutifan and NKT2152, rapidly ameliorated hypercalcemia and cachexia in patients with ccRCC, including in some who did not exhibit objective tumor shrinkage. Our findings support prospective clinical studies to determine whether HIF2 inhibitors can be leveraged not only for tumor control, but also for the treatment of cancer-associated cachexia in renal cell carcinoma.

Nature MedicineVol. 32(1)
Broad Institute (US), Beth Israel Deaconess Medical Center (US), Howard Hughes Medical Institute (US), Harvard University (US), University of Massachusetts Chan Medical School (US), Dana-Farber Cancer Institute (US), Dana-Farber/Harvard Cancer Center (US), Io Therapeutics (United States) (US)
Openalex Percentile: Top 8%
Cancer, Hypoxia, and Metabolism
2.81
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