Chou Wesley H, Chakiryan Nicholas H, Thomas George V
Department of Urology, Oregon Health & Science University, Portland, Oregon.
Knight Cancer Institute, Oregon Health & Science University, Portland, Oregon.
J Kidney Cancer VHL. 2025 May 5;12(2):37-45. doi: 10.15586/jkc.v12i2.386. eCollection 2025.
While vascular endothelial growth factor tyrosine kinase inhibitors (VEGF-TKIs) are a mainstay of treatment for advanced renal cell carcinoma (RCC), mechanisms of resistance to VEGF-TKIs remain under ongoing investigation. To assess transcriptomic changes in clear-cell RCC (ccRCC) and non-ccRCC exposed to a VEGF-TKI, we analyzed differential single-cell gene expression in RCC tumor-organoids exposed to cabozantinib versus control solvent. In ccRCC organoid cells, was notably highly associated with cabozantinib exposure (log2 fold-change 2.18, detected proportion 0.52 vs. 0.23, false-detection rate adjusted p<0.001). Importantly, our findings were independently validated in a recent study of advanced ccRCC patients treated with cabozantinib, which demonstrated that higher expression was significantly associated with decreased tumor response and less robust reduction of VEGF expression. has been shown to mediate VEGF secretion in a separate study and may potentiate compensatory angiogenesis after cabozantinib exposure. Gene expression scores were then developed based on transcriptomic changes associated with cabozantinib exposure and applied to stage IV patients in several independent cohorts. Higher scores were significant predictors of worse overall survival in TCGA non-RCC patients and worse progression-free survival in JAVELIN Renal 101 ccRCC patients. Overall, this experiment represents an incremental step in a larger effort to elucidate resistance mechanisms to VEGF-TKIs.
虽然血管内皮生长因子酪氨酸激酶抑制剂(VEGF-TKIs)是晚期肾细胞癌(RCC)治疗的主要手段,但对VEGF-TKIs的耐药机制仍在持续研究中。为了评估暴露于VEGF-TKI的透明细胞RCC(ccRCC)和非ccRCC中的转录组变化,我们分析了暴露于卡博替尼与对照溶剂的RCC肿瘤类器官中的差异单细胞基因表达。在ccRCC类器官细胞中, 与卡博替尼暴露显著高度相关(log2倍数变化2.18,检测比例0.52对0.23,错误发现率调整后p<0.001)。重要的是,我们的发现最近在一项对接受卡博替尼治疗的晚期ccRCC患者的研究中得到了独立验证,该研究表明较高的 表达与肿瘤反应降低和VEGF表达降低不明显显著相关。在另一项研究中已表明 可介导VEGF分泌,并且在卡博替尼暴露后可能增强代偿性血管生成。然后根据与卡博替尼暴露相关的转录组变化开发基因表达评分,并应用于几个独立队列中的IV期患者。较高的评分是TCGA非RCC患者总生存期较差以及JAVELIN Renal 101 ccRCC患者无进展生存期较差的显著预测指标。总体而言,该实验是为阐明对VEGF-TKIs耐药机制所做的更大努力中的一个渐进步骤。 (原文中部分内容缺失,请根据实际情况补充完整后理解。)