Tanreqing suppresses the proliferation and migration of non-small cell lung cancer cells by mediating the inactivation of the HIF1α signaling pathway via exosomal circ-WDR78

被引:7
作者
Hong, Weijun [1 ]
Du, Kaifeng [1 ]
Zhang, Qingqing [1 ]
Ren, Zhiguo [2 ,3 ]
Gao, Xiwen [1 ,4 ]
机构
[1] Fudan Univ, Minhang Hosp, Dept Pulm & Crit Care Med, Shanghai, Peoples R China
[2] No 971 Hosp Peoples Liberat Army Navy, Dept Resp Med, Qingdao, Shandong, Peoples R China
[3] No 971 Hosp Peoples Liberat Army Navy, Dept Resp Med, 22 Minjiang Rd, Qingdao 266071, Shandong, Peoples R China
[4] Fudan Univ No, Minhang Hosp, Dept Pulm & Crit Care Med, 170 Xinsong Rd, Shanghai 201199, Peoples R China
关键词
TRQ; NSCLC; exosome; circ-WDR78; HIF1 alpha signaling pathway; PROGRESSION; RESISTANCE; CIRCRNAS; MEDICINE;
D O I
10.1080/07391102.2023.2301514
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Circular RNAs (circRNAs) have emerged as regulators of cancer progression, including non-small cell lung cancer (NSCLC). Tanreqing (TRQ), a traditional Chinese medicine, is used clinically for respiratory diseases. RT-qPCR quantified circ-WDR78 expression in NSCLC cells. Cell growth, apoptosis, invasion, and migration were assessed by functional assays. RNA-binding protein immunoprecipitation (RIP), luciferase reporter, and RNA pull-down assays determined the competing endogenous RNA (ceRNA) network of circ-WDR78. The interaction between HIF1 alpha and CD274 (PD-L1) promoter was analyzed by chromatin immunoprecipitation (ChIP). Circ-WDR78 expression was up-regulated in TRQ-treated NSCLC cells. Functionally, circ-WDR78 exhibited anti-tumor effects in these cells. Additionally, circ-WDR78 could also induce reactive oxygen species (ROS) accumulation by down-regulating HIF1 alpha expression, promoting autophagy. Mechanistically, circ-WDR78 destabilizes HIF1 alpha via the miR-1265/FBXW8 axis. TRQ-induced exosome secretion from NSCLC cells inhibits PD-L1 expression, preventing immune escape. We found that TRQ-treated NSCLC cells secrete exosomes to transmit circ-WDR78 to untreated NSCLC cells, inhibiting the malignancy of recipient tumor cells. In conclusion, TRQ inhibits NSCLC cell proliferation, invasion, and migration through exosomal circ-WDR78-mediated inactivation of the HIF1 alpha signaling pathway, providing potential insight into TRQ injection for NSCLC treatment.
引用
收藏
页码:2491 / 2502
页数:12
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