Propofol suppresses growth, migration and invasion of A549 cells by down-regulation of miR-372

被引:51
作者
Sun, Hai [1 ]
Gao, Dengyu [1 ]
机构
[1] Jilin Univ, China Japan Union Hosp, Dept Anesthesiol, 126 Xiantai St, Changchun 130033, Jilin, Peoples R China
关键词
Lung cancer; Propofol; microRNA-372; Wnt/beta-catenin pathway; mTOR signaling pathway; LUNG-CANCER; HEPATOCELLULAR-CARCINOMA; TUMOR-SUPPRESSOR; PATHWAY; APOPTOSIS; EXPRESSION; STRESS;
D O I
10.1186/s12885-018-5175-y
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundPropofol, a commonly used intravenous anesthetic during cancer resection surgery, has been found to exhibit tumor inhibitory effects in vitro and in vivo. The role of propofol in lung cancer has been previously reported, whereas its action mechanism remains unclear. This study further investigated the effects of propofol on lung cancer A549 cell growth, migration and invasion, as well as the underlying mechanisms.MethodsCell viability, proliferation, migration, invasion and apoptosis were assessed by CCK-8 assay, BrdU assay, two chamber transwell assay and flow cytometry, respectively. The regulatory effect of propofol on microRNA-372 (miR-372) expression in A549 cells was analyzed by qRT-PCR. Cell transfection was used to change the expression of miR-372. The protein expression of key factors involving in cell proliferation, apoptosis, migration and invasion, as well as Wnt/-catenin and mTOR pathways were analyzed by western blotting.ResultsPropofol inhibited lung cancer A549 cell viability, proliferation, migration, and invasion, but promoted cell apoptosis. Moreover, miR-372 was down-regulated in propofol-treated A549 cells. Overexpression of miR-372 abrogated the effects of propofol on proliferation, migration, invasion and apoptosis of A549 cells. Knockdown of miR-372 had opposite effects. Furthermore, propofol suppressed Wnt/-catenin and mTOR signaling pathways by down-regulating miR-372.ConclusionPropofol inhibits growth, migration and invasion of lung cancer A549 cells at least in part by down-regulating miR-372 and then inactivating Wnt/-catenin and mTOR pathways.
引用
收藏
页数:11
相关论文
共 38 条
[1]   RETRACTED: microRNA-145-3p inhibits non-small cell lung cancer cell migration and invasion by targeting PDK1 via the mTOR signaling pathway (Retracted article. See vol. 122, 2021) [J].
Chen, Gui-Min ;
Zheng, A-Juan ;
Cai, Jing ;
Han, Ping ;
Ji, Hong-Bo ;
Wang, Le-Le .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2018, 119 (01) :885-895
[2]   miR-372 regulates cell cycle and apoptosis of ags human gastric cancer cell line through direct regulation of LATS2 [J].
Cho, Wha Ja ;
Shin, Jeong Min ;
Kim, Jong Soo ;
Lee, Man Ryul ;
Hong, Ki Sung ;
Lee, Jun-Ho ;
Koo, Kyoung Hwa ;
Park, Jeong Woo ;
Kim, Kye-Seong .
MOLECULES AND CELLS, 2009, 28 (06) :521-527
[3]  
Cui D, 2012, PLOS ONE, V7, P11
[4]   Propofol induces endoplasmic reticulum (ER) stress and apoptosis in lung cancer cell H460 [J].
Cui, Wen-Yao ;
Liu, Yan ;
Zhu, Yong-Qiang ;
Song, Tao ;
Wang, Qiu-Shi .
TUMOR BIOLOGY, 2014, 35 (06) :5213-5217
[5]  
Du Q, 2018, BRAZ J MED BIOL RES, V51, DOI [10.1590/1414-431X20176803, 10.1590/1414-431x20176803]
[6]   Review of Propofol and Auxiliary Medications Used for Sedation [J].
Ellett, Marsha L. .
GASTROENTEROLOGY NURSING, 2010, 33 (04) :284-295
[7]  
Forde PM, 2013, EXPERT REV ANTICANC, V13, P745, DOI [10.1586/ERA.13.47, 10.1586/era.13.47]
[8]   Targeting PI3K/AKT/mTOR pathway in non small cell lung cancer [J].
Fumarola, Claudia ;
Bonelli, Mara A. ;
Petronini, Pier Giorgio ;
Alfieri, Roberta R. .
BIOCHEMICAL PHARMACOLOGY, 2014, 90 (03) :197-207
[9]   Upregulation of microRNA-372 associates with tumor progression and prognosis in hepatocellular carcinoma [J].
Gu, Hao ;
Guo, Xiaodong ;
Zou, Lin ;
Zhu, Haiyan ;
Zhang, Jinhui .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 2013, 375 (1-2) :23-30
[10]   Anesthetic Propofol Reduces Endotoxic Inflammation by Inhibiting Reactive Oxygen Species-regulated Akt/IKKβ/NF-κB Signaling [J].
Hsing, Chung-Hsi ;
Lin, Ming-Chung ;
Choi, Pui-Ching ;
Huang, Wei-Ching ;
Kai, Jui-In ;
Tsai, Cheng-Chieh ;
Cheng, Yi-Lin ;
Hsieh, Chia-Yuan ;
Wang, Chi-Yun ;
Chang, Yu-Ping ;
Chen, Yu-Hong ;
Chen, Chia-Ling ;
Lin, Chiou-Feng .
PLOS ONE, 2011, 6 (03)