作者
Le Qu,Jin Ding,Cheng Chen,Zhenjie Wu,Bing Liu,Yi Gao,Wei Chen,Feng Liu,Wen Sun,Xiaofeng Li,Xue Wang,Yue Wang,Zhenyu Xu,Li Gao,Qing Yang,Bin Xu,Yaoming Li,Ziyu Fang,Zhipeng Xu,Yi Bao,Da-Yu Wu,Min Xiong,Hao Sun,Yinghao Sun,Hongyang Wang,Linhui Wang
摘要
Sunitinib resistance is a major challenge for advanced renal cell carcinoma (RCC). Understanding the underlying mechanisms and developing effective strategies against sunitinib resistance are highly desired in the clinic. Here we identified an lncRNA, named lncARSR (lncRNA Activated in RCC with Sunitinib Resistance), which correlated with clinically poor sunitinib response. lncARSR promoted sunitinib resistance via competitively binding miR-34/miR-449 to facilitate AXL and c-MET expression in RCC cells. Furthermore, bioactive lncARSR could be incorporated into exosomes and transmitted to sensitive cells, thus disseminating sunitinib resistance. Treatment of sunitinib-resistant RCC with locked nucleic acids targeting lncARSR or an AXL/c-MET inhibitor restored sunitinib response. Therefore, lncARSR may serve as a predictor and a potential therapeutic target for sunitinib resistance.