LINC00205 Promotes Tumor Malignancy of Lung Adenocarcinoma Through Sponging miR-185-5p

被引:6
作者
Li, Yongqiang [1 ]
Hu, Yahui [2 ]
Wu, Yuting [1 ]
Zhang, Deming [2 ]
Huang, Dongwei [2 ]
机构
[1] PLA Gen Hosp Southern Theatre Command, Dept Resp Med, Guangzhou, Guangdong, Peoples R China
[2] PLA Gen Hosp Southern Theatre Command, Dept Geriatr Resp Med, Guangzhou, Guangdong, Peoples R China
关键词
LINC00205; lung adenocarcinoma; tumor malignancy; miR-185-5p; LONG NONCODING RNA; CANCER; PROLIFERATION; PROGRESSION; METASTASIS; EXPRESSION; CARCINOMA; SURVIVAL; LNCRNAS; PROTEIN;
D O I
10.1093/labmed/lmab041
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
The emerging role of long noncoding RNAs (lncRNAs) in cancer, especially in lung adenocarcinoma (LUAD), is attracting increasingly more attention as a potential therapeutic target. However, whether lncRNA LINC00205 regulates the malignancy of LUAD has not been characterized. In this study, we discovered that LINC00205 was markedly upregulated in LUAD tissues and cell lines and correlated with poor prognosis of patients with LUAD. Our data showed that LINC00205 promoted the migration and proliferation of LUAD cells in vitro and tumor growth in vivo. Notably, the tumor suppressor miR-185-5p was found to be a direct target of LINC00205. In addition, miR-185-5p diminished the promotion of cell proliferation and migration mediated by LINC00205, whereas miR-185-5p inhibition had the opposite effect. In summary, our results show that LINC00205 contributes to LUAD malignancy by sponging miR-185-5p, which provides new insight into LUAD progression.
引用
收藏
页码:39 / 46
页数:8
相关论文
共 37 条
  • [11] MALAT-1, a novel noncoding RNA, and thymosin β4 predict metastasis and survival in early-stage non-small cell lung cancer
    Ji, P
    Diederichs, S
    Wang, WB
    Böing, S
    Metzger, R
    Schneider, PM
    Tidow, N
    Brandt, B
    Buerger, H
    Bulk, E
    Thomas, M
    Berdel, WE
    Serve, H
    Müller-Tidow, C
    [J]. ONCOGENE, 2003, 22 (39) : 8031 - 8041
  • [12] Joshi Pooja, 2014, World J Methodol, V4, P59, DOI 10.5662/wjm.v4.i2.59
  • [13] Functional annotation of noncoding variants and prioritization of cancer-associated lncRNAs in lung cancer
    Li, Hua
    Lv, Xin
    [J]. ONCOLOGY LETTERS, 2016, 12 (01) : 222 - 230
  • [14] TANRIC: An Interactive Open Platform to Explore the Function of lncRNAs in Cancer
    Li, Jun
    Han, Leng
    Roebuck, Paul
    Diao, Lixia
    Liu, Lingxiang
    Yuan, Yuan
    Weinstein, John N.
    Liang, Han
    [J]. CANCER RESEARCH, 2015, 75 (18) : 3728 - 3737
  • [15] starBase v2.0: decoding miRNA-ceRNA, miRNA-ncRNA and protein-RNA interaction networks from large-scale CLIP-Seq data
    Li, Jun-Hao
    Liu, Shun
    Zhou, Hui
    Qu, Liang-Hu
    Yang, Jian-Hua
    [J]. NUCLEIC ACIDS RESEARCH, 2014, 42 (D1) : D92 - D97
  • [16] Control of RNA processing by a large non-coding RNA over-expressed in carcinomas
    Lin, Rui
    Roychowdhury-Saha, Manami
    Black, Chris
    Watt, Andrew T.
    Marcusson, Eric G.
    Freier, Susan M.
    Edgington, Thomas S.
    [J]. FEBS LETTERS, 2011, 585 (04): : 671 - 676
  • [17] LINC00205 modulates the expression of EPHX1 through the inhibition of miR-184 in hepatocellular carcinoma as a ceRNA
    Long, Xi
    Li, Qian
    Zhi, Li-Jun
    Li, Jin-Mao
    Wang, Zheng-Yu
    [J]. JOURNAL OF CELLULAR PHYSIOLOGY, 2020, 235 (03) : 3013 - 3021
  • [18] Long noncoding RNA SNHG1 promotes non-small cell lung cancer progression by up-regulating MTDH via sponging miR-145-5p
    Lu, Qingchun
    Shan, Shan
    Li, Yanyan
    Zhu, Dongyi
    Jin, Wenjing
    Ren, Tao
    [J]. FASEB JOURNAL, 2018, 32 (07) : 3957 - 3967
  • [19] Long non-coding RNAs: insights into functions
    Mercer, Tim R.
    Dinger, Marcel E.
    Mattick, John S.
    [J]. NATURE REVIEWS GENETICS, 2009, 10 (03) : 155 - 159
  • [20] No-Nonsense Functions for Long Noncoding RNAs
    Nagano, Takashi
    Fraser, Peter
    [J]. CELL, 2011, 145 (02) : 178 - 181