Ciclopirox induces autophagy through reactive oxygen species-mediated activation of JNK signaling pathway
文献类型:期刊论文
作者 | Zhou, Hongyu1,2; Shen, Tao2; Shang, Chaowei2; Luo, Yan2; Liu, Lei2; Yan, Juming1; Li, Yan1![]() |
刊名 | ONCOTARGET
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出版日期 | 2014-10-30 |
卷号 | 5期号:20页码:10140-10150 |
关键词 | Ciclopirox autophagy rhabdomyosarcoma reactive oxygen species JNK |
英文摘要 | Ciclopirox olamine (CPX), a fungicide, has been demonstrated as a potential anticancer agent. However, the underlying anticancer mechanism is not well understood. Here, we found that CPX induced autophagy in human rhabdomyosarcoma (Rh30 and RD) cells. It appeared that CPX-induced autophagy was attributed to induction of reactive oxygen species (ROS), as N-acetyl-L-cysteine (NAC), a ROS scavenger and antioxidant, prevented this process. Furthermore, we observed that CPX induced activation of mitogen-activated protein kinases (MAPKs), including extracellular signal-regulated kinase 1/2 (ERK1/2), c-Jun N-terminal kinase (JNK) and p38 MAPK, which was also blocked by NAC. However, only inhibition of JNK (with SP600125) or expression of dominant negative c-Jun partially prevented CPX-induced autophagy, indicating that ROS-mediated activation of JNK signaling pathway contributed to CPX-induced autophagy. Of interest, inhibition of autophagy by chloroquine (CQ) enhanced CPX-induced cell death, indicating that CPX-induced autophagy plays a pro-survival role in human rhabdomyosarcoma cells. Our finding suggests that the combination with autophagy inhibitors may be a novel strategy in potentiating the anticancer activity of CPX for treatment of rhabdomyosarcoma. |
类目[WOS] | Oncology ; Cell Biology |
研究领域[WOS] | Oncology ; Cell Biology |
关键词[WOS] | ENDOPLASMIC-RETICULUM STRESS ; OXIDATIVE STRESS ; CELL-DEATH ; CANCER-CELLS ; FUNGICIDE CICLOPIROX ; PROTEIN PHOSPHATASES ; INDUCED APOPTOSIS ; TRANSDUCTION ; EXPRESSION ; SURVIVAL |
收录类别 | SCI |
语种 | 英语 |
WOS记录号 | WOS:000348036500048 |
公开日期 | 2015-07-07 |
源URL | [http://ir.kib.ac.cn/handle/151853/20414] ![]() |
专题 | 昆明植物研究所_植物化学与西部植物资源持续利用国家重点实验室 |
作者单位 | 1.Chinese Acad Sci, Kunming Inst Bot, State Key Lab Phytochem & Plant Resources West Ch, Kunming 650201, Peoples R China 2.Louisiana State Univ, Hlth Sci Ctr, Dept Biochem & Mol Biol, Shreveport, LA 71130 USA 3.Louisiana State Univ, Hlth Sci Ctr, Feist Weiller Canc Ctr, Shreveport, LA 71130 USA |
推荐引用方式 GB/T 7714 | Zhou, Hongyu,Shen, Tao,Shang, Chaowei,et al. Ciclopirox induces autophagy through reactive oxygen species-mediated activation of JNK signaling pathway[J]. ONCOTARGET,2014,5(20):10140-10150. |
APA | Zhou, Hongyu.,Shen, Tao.,Shang, Chaowei.,Luo, Yan.,Liu, Lei.,...&Huang, Shile.(2014).Ciclopirox induces autophagy through reactive oxygen species-mediated activation of JNK signaling pathway.ONCOTARGET,5(20),10140-10150. |
MLA | Zhou, Hongyu,et al."Ciclopirox induces autophagy through reactive oxygen species-mediated activation of JNK signaling pathway".ONCOTARGET 5.20(2014):10140-10150. |
入库方式: OAI收割
来源:昆明植物研究所
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