lncRNA-ATB functions as a competing endogenous RNA to promote YAP1 by sponging miR-590-5p in malignant melanoma

被引:52
作者
Mou, Kuanhou [1 ]
Liu, Bo [2 ]
Ding, Meiling [3 ]
Mu, Xin [1 ]
Han, Dan [1 ]
Zhou, Yan [1 ]
Wang, Li-Juan [1 ]
机构
[1] Xi An Jiao Tong Univ, Affiliated Hosp 1, Dept Dermatol, 277 Yanta West Rd, Xian 710061, Shaanxi, Peoples R China
[2] Yanan Tradit Chinese Med Hosp, Dept Dermatol, Yanan 716000, Shaanxi, Peoples R China
[3] Fourth Mil Med Univ, Xijing Hosp Digest Dis, Natl Clin Res Ctr Digest Dis, State Key Lab Canc Biol, Xian 710032, Shaanxi, Peoples R China
关键词
malignant melanoma; lncRNA-ATB; microRNA-590-5p; YAP1; competing endogenous RNA; LONG NONCODING RNA; INVASION-METASTASIS CASCADE; CANCER CELL-PROLIFERATION; POOR-PROGNOSIS; HIGH EXPRESSION; TGF-BETA; PROGRESSION; MIGRATION; RESISTANCE; NETWORKS;
D O I
10.3892/ijo.2018.4454
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The critical long non-coding RNAs (lncRNAs) involved in the carcinogenesis and progression of malignant melanoma (MM) have not been fully investigated. In the present study, it was identified that lncRNA activated by transforming growth factor- (lncRNA-ATB) was upregulated in MM tissues and cells compared with benign nevus cells and human melanocytes, via comparative lncRNA screening from Gene Expression Omnibus datasets and reverse transcription-quantitative polymerase chain reaction analysis. Furthermore, lncRNA-ATB promoted the cell proliferation, cell migration, and cell invasion of MM cells in vitro, and tumor growth in vivo. It was additionally identified that lncRNA-ATB attenuated cell cycle arrest and inhibited cellular apoptosis in MM cells. Finally, it was demonstrated that lncRNA-ATB functions as a competing endogenous RNA (ceRNA) to enhance Yes associated protein 1 expression by competitively sponging microRNA miR-590-5p in MM cells. In conclusion, the present study revealed the expression and roles of lncRNA-ATB in MM, and indicated that lncRNA-ATB functions as a ceRNA to promote MM proliferation and invasion by sponging miR-590-5p.
引用
收藏
页码:1094 / 1104
页数:11
相关论文
共 50 条
[1]  
[Anonymous], 1996, GUIDE CARE USE LAB A
[2]   Final Version of 2009 AJCC Melanoma Staging and Classification [J].
Balch, Charles M. ;
Gershenwald, Jeffrey E. ;
Soong, Seng-jaw ;
Thompson, John F. ;
Atkins, Michael B. ;
Byrd, David R. ;
Buzaid, Antonio C. ;
Cochran, Alistair J. ;
Coit, Daniel G. ;
Ding, Shouluan ;
Eggermont, Alexander M. ;
Flaherty, Keith T. ;
Gimotty, Phyllis A. ;
Kirkwood, John M. ;
McMasters, Kelly M. ;
Mihm, Martin C., Jr. ;
Morton, Donald L. ;
Ross, Merrick I. ;
Sober, Arthur J. ;
Sondak, Vernon K. .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (36) :6199-6206
[3]   Long Noncoding RNA and Cancer: A New Paradigm [J].
Bhan, Arunoday ;
Soleimani, Milad ;
Mandal, Subhrangsu S. .
CANCER RESEARCH, 2017, 77 (15) :3965-3981
[4]  
Bian DH, 2017, AM J CANCER RES, V7, P28
[5]   Long Noncoding RNAs as Biomarkers in Cancer [J].
Bolha, Luka ;
Ravnik-Glavac, Metka ;
Glavac, Damjan .
DISEASE MARKERS, 2017, 2017
[6]   Downregulation of microRNA let-7f mediated the Adriamycin resistance in leukemia cell line [J].
Cao, Yi-Xiong ;
Wen, Feng ;
Luo, Ze-Yu ;
Long, Xing-Xing ;
Luo, Cong ;
Liao, Pei ;
Li, Jun-Jun .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2020, 121 (10) :4022-4033
[7]  
Chen XJ, 2017, AM J TRANSL RES, V9, P90
[8]   LncROR Promotes Bladder Cancer Cell Proliferation, Migration, and EpithelialMesenchymal Transition [J].
Chen, Yi ;
Peng, Ya ;
Xu, Zhipeng ;
Ge, Bo ;
Xiang, Xuebao ;
Zhang, Tianyu ;
Gao, Li ;
Shi, Hailin ;
Wang, Chuang ;
Huang, Jiefu .
CELLULAR PHYSIOLOGY AND BIOCHEMISTRY, 2017, 41 (06) :2399-2410
[9]   Suppression of PDCD4 mediated by the long non-coding RNA HOTAIR inhibits the proliferation and invasion of glioma cells [J].
Chen, Yong'an ;
Bian, Yusong ;
Zhao, Shanpeng ;
Kong, Fanqiang ;
Li, Xin'gang .
ONCOLOGY LETTERS, 2016, 12 (06) :5170-5176
[10]   lncRNA CCAT1 Promotes Glioma Tumorigenesis by Sponging miR-181b [J].
Cui, Bingzhou ;
Li, Baoshan ;
Liu, Qi ;
Cui, Youqiang .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2017, 118 (12) :4548-4557