舒尼替尼
癌症研究
肾细胞癌
体内
下调和上调
细胞内
溶血磷脂酸
癌症
小RNA
生物
医学
内科学
基因
细胞生物学
受体
生物化学
生物技术
作者
Kangbo Huang,Yihui Pan,Guannan Shu,Haohua Yao,Xi Liu,Mi Zhou,Jinhuan Wei,Zhenhua Chen,Jun Lü,Zihao Feng,Wei Ma,Hui Han,Zhousan Zheng,Junhang Luo,Jiaxing Zhang
标识
DOI:10.1016/j.canlet.2021.10.003
摘要
Sunitinib resistance is a major challenge in systemic therapy for renal cell carcinoma (RCC). The role of circular RNAs (circRNAs) in regulating sunitinib resistance of RCC is largely unknown. We established sunitinib-resistant RCC cell lines in vivo. Through RNA-sequencing, we identified circSNX6, whose expression is upregulated in sunitinib-resistant cells compared with their parental cells. High circSNX6 expression was correlated with sunitinib resistance and worse oncologic outcomes in a cohort of 81 RCC patients. In vitro and in vivo experiments confirmed that circSNX6 could promote sunitinib resistance in RCC. circSNX6 acts as a molecular "sponge" to relieve the suppressive effect of microRNA (miR)-1184 on its target gene, glycerophosphocholine phosphodiesterase 1 (GPCPD1), which increases intracellular lysophosphatidic acid (LPA) levels and, ultimately, promotes sunitinib resistance in RCC cells. Our findings demonstrated that the circSNX6/miR-1184/GPCPD1 axis had a critical role in regulation of intracellular LPA levels and sunitinib resistance in RCC; they also provide a novel prognostic indicator and promising therapeutic targets.
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