Long Noncoding RNA Small Nucleolar RNA Host Gene 6 Promotes Cell Proliferation, Migration and Invasion in Melanoma by Sponging miR-944

被引:0
作者
Zhu, Jinjin [1 ,2 ]
Xu, Pan [3 ]
机构
[1] Nantong Univ, Sch Med, Nantong 226001, Jiangsu, Peoples R China
[2] Nantong Univ, Affiliated Hosp, Dept Dermatol, Nantong 226000, Jiangsu, Peoples R China
[3] Nantong Univ, Affiliated Hosp, Dept Med Cosmetol, Nantong 226000, Jiangsu, Peoples R China
关键词
Melanoma; SNHG6; miR-944; Proliferation; Migration and Invasion; PREDICTS; LNCRNA;
D O I
10.1166/jbt.2021.2615
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Long noncoding RNA small nucleolar RNA host gene 6 (SNHG6) has been reported to be a tumor promoter in various human cancers. Nevertheless, the detailed functions and clinical value of SNHG6 in melanoma remain elusive. The study aimed to investigate the role and potential mechanism of SNHG6 in melanoma metastasis. Quantitative real-time PCR (qRT-PCR) was used to detect the expressions of SNHG6 and miR-944 in melanoma cells. Cell proliferation was evaluated by Cell Counting Kit-8 (CCK-8) assay, and cell migration and invasion were measured by wound healing assay and cell invasion assay, respectively. In addition, dual luciferase reporter assay was performed to verify the interaction between SNHG6 and miR-944. The protein expressions of PI3K/Akt pathway were evaluated by western blot assay. The results revealed that SNHG6 expression was significantly increased in melanoma cells. Knockdown of SNHG6 suppressed cell proliferation, migration and invasion in A375 cells. Moreover, miR-944 was identified as a direct target of SNHG6 in melanoma. miR-944 was downregulated in melanoma cells, while SNHG6 silencing improved miR-944 level in A375 cells. Rescue experiments demonstrated that miR-944 overexpression reversed the effects of SNHG6 on A375 cell proliferation, migration and invasion. Altogether, SNHG6 exerted oncogenic effects in melanoma cells, providing a novel promising target for the treatment of melanoma.
引用
收藏
页码:1459 / 1465
页数:7
相关论文
共 28 条
[1]  
[Anonymous], 2015, LANCET, V385, P2323, DOI 10.1016/S0140-6736(15)61087-X
[2]  
Arunkumar G, 2017, BIOMED REP, V6, P455, DOI 10.3892/br.2017.876
[3]   Long Noncoding RNAs: Cellular Address Codes in Development and Disease [J].
Batista, Pedro J. ;
Chang, Howard Y. .
CELL, 2013, 152 (06) :1298-1307
[4]   A Long Noncoding RNA Controls Muscle Differentiation by Functioning as a Competing Endogenous RNA [J].
Cesana, Marcella ;
Cacchiarelli, Davide ;
Legnini, Ivano ;
Santini, Tiziana ;
Sthandier, Olga ;
Chinappi, Mauro ;
Tramontano, Anna ;
Bozzoni, Irene .
CELL, 2011, 147 (02) :358-369
[5]   STAT3-induced upregulation of lncRNA SNHG17 predicts a poor prognosis of melanoma and promotes cell proliferation and metastasis through regulating PI3K-AKT pathway [J].
Gao, H. ;
Liu, R. ;
Sun, X. .
EUROPEAN REVIEW FOR MEDICAL AND PHARMACOLOGICAL SCIENCES, 2019, 23 (18) :8000-8010
[6]   LncRNA SNHG5 promotes growth and invasion in melanoma by regulating the miR-26a-5p/TRPC3 pathway [J].
Gao, Jun ;
Zeng, Kang ;
Liu, Yi ;
Gao, Lin ;
Liu, Lishi .
ONCOTARGETS AND THERAPY, 2019, 12 :169-179
[7]   HOTAIR: an oncogenic long non-coding RNA in different cancers [J].
Hajjari, Mohammadreza ;
Salavaty, Abbas .
CANCER BIOLOGY & MEDICINE, 2015, 12 (01) :1-9
[8]   Large non-coding RNAs: missing links in cancer? [J].
Huarte, Maite ;
Rinn, John L. .
HUMAN MOLECULAR GENETICS, 2010, 19 :R152-R161
[9]   Extensive and coordinated transcription of noncoding RNAs within cell-cycle promoters [J].
Hung, Tiffany ;
Wang, Yulei ;
Lin, Michael F. ;
Koegel, Ashley K. ;
Kotake, Yojiro ;
Grant, Gavin D. ;
Horlings, Hugo M. ;
Shah, Nilay ;
Umbricht, Christopher ;
Wang, Pei ;
Wang, Yu ;
Kong, Benjamin ;
Langerod, Anita ;
Borresen-Dale, Anne-Lise ;
Kim, Seung K. ;
van de Vijver, Marc ;
Sukumar, Saraswati ;
Whitfield, Michael L. ;
Kellis, Manolis ;
Xiong, Yue ;
Wong, David J. ;
Chang, Howard Y. .
NATURE GENETICS, 2011, 43 (07) :621-U196
[10]  
Ke D., 2019, PATHOL ONCOL RES