Abu-Remaileh Muhannad, Stransky Laura A, Bhalerao Nikita, Shirole Nitin H, Jiang Qinqin, Saad Eddy, Machaalani Marc, Vigeant Sean M, Woldemichael Hilina, Xu Charles, Lu Jing, Wei Hairong, Liu Zhihong, Sun William, Enomoto Kei, Choueiri Toni K, Pitarresi Jason R, Carr Steven A, Udeshi Namrata D, Kaelin William G
bioRxiv. 2025 Sep 11:2025.09.09.675147. doi: 10.1101/2025.09.09.675147.
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, is frequently caused by loss of the pVHL tumor suppressor protein and the resulting upregulation of the HIF2 transcription factor. We show that , which resides on a ccRCC amplicon on chromosome 12p, is a direct HIF2 transcriptional target in ccRCC. Further, we show that the increased 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 ccRCC patients, including in some patients who did not exhibit objective tumor shrinkage.
肾癌常引发副肿瘤综合征,包括高钙血症和恶病质,但其潜在机制尚未完全明确。最常见的肾癌类型,即透明细胞肾细胞癌,通常是由于pVHL肿瘤抑制蛋白缺失以及由此导致的HIF2转录因子上调所致。我们发现,位于12号染色体p臂上ccRCC扩增子上的 ,是ccRCC中HIF2的直接转录靶点。此外,我们还表明,在临床前原位细胞系肿瘤模型中, 表达增加对于诱导高钙血症和恶病质既是必要的也是充分的。与这些观察结果一致,两种不同的变构HIF2抑制剂,即belzutifan和NKT2152,迅速改善了ccRCC患者的高钙血症和恶病质,包括一些未出现客观肿瘤缩小的患者。