Long non-coding RNA H19 promotes the proliferation and invasion of lung cancer cells and regulates the expression of E-cadherin, N-cadherin, and vimentin

被引:35
作者
Liaol, Shu [1 ]
Yu, Chaxiu [2 ]
Liu, Hucheng [3 ]
Zhang, Congkai [1 ]
Li, Yong [1 ]
Zhongl, Xiaojun [1 ]
机构
[1] Nanchang Univ, Dept Med Oncol, Affiliated Hosp 1, 17 Yongwai Zheng St, Nanchang 330006, Jiangxi, Peoples R China
[2] Nanchang Univ, Dept Anesthesiol, Affiliated Hosp 1, Nanchang 330006, Jiangxi, Peoples R China
[3] Nanchang Univ, Dept Osseous & Soft Tissue Oncol, Affiliated Hosp 1, Nanchang 330006, Jiangxi, Peoples R China
基金
中国国家自然科学基金;
关键词
long non-coding RNA; lung cancer; E-cadherin; N-cadherin; vimentin; EPITHELIAL-MESENCHYMAL TRANSITION; LNCRNA H19; METASTASIS; EMT;
D O I
10.2147/OTT.S185156
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
Background: This study aimed to explore the effect of long non-coding RNA (LncRNA) H19 on the proliferation and invasion of lung carcinoma cells A549, and to determine its molecular targets. Methods: A549 cells were with either LncRNA H19 or LncRNA H19 shRNA, and the expression levels of LncRNA H19 were evaluated by quantitative real-time PCR (RT-PCR). We measured cell proliferation using the CCK-8 assay, cell counting assays, and colony formation assay in response to shLncRNA H19-2. Cell migration and invasion were assessed by wound healing assay and Transwell assay, respectively. The mRNA and protein expression levels of E-cadherin, N-cadherin, and vimentin were determined by RT-PCR and western blot, respectively. Results: The three LncRNA H19 shRNAs used in our study significantly reduced the expression levels of LncRNA H19 in A549 cells (P<0.05). Moreover, LncRNA H19 shRNA 2 (shLncRNA-2) was the most potent inhibitor of LncRNA H19 expression, and was selected for further experimentation. Transfection with shLncRNA H19-2 significantly decreased the proliferation, migration, and invasion of A549 cells, while overexpression of LncRNA H19 had the opposite effect in these cells (P<0.05). In response to shLncRNA H19-2, the expression levels of E-cadherin were notably elevated (P<0.05), while the expression levels of N-cadherin and vimentin were decreased (P<0.05). In contrast, overexpression of LncRNA H19 induced the expression of E-cadherin, and blocked the expression of N-cadherin, and vimentin (P<0.05). Conclusion: Our results suggest that LncRNA H19 mediates the proliferation and invasion of lung cancer cells via upregulation of N-cadherin and vimentin, and downregulation of E-cadherin.
引用
收藏
页码:4099 / 4106
页数:8
相关论文
共 26 条
[1]
Immunoexpression of Epithelial Mesenchymal Transition Proteins E-Cadherin, -Catenin, and N-Cadherin in Oral Squamous Cell Carcinoma [J].
Angadi, Punnya V. ;
Patil, Prakash V. ;
Angadi, Vidya ;
Mane, Deepa ;
Shekar, Saurabh ;
Hallikerimath, Seema ;
Kale, Alka D. ;
Kardesai, S. G. .
INTERNATIONAL JOURNAL OF SURGICAL PATHOLOGY, 2016, 24 (08) :696-703
[2]
miR-31 and its host gene lncRNA LOC554202 are regulated by promoter hypermethylation in triple-negative breast cancer [J].
Augoff, Katarzyna ;
McCue, Brian ;
Plow, Edward F. ;
Sossey-Alaoui, Khalid .
MOLECULAR CANCER, 2012, 11
[3]
Regulatory networks defining EMT during cancer initiation and progression [J].
De Craene, Bram ;
Berx, Geert .
NATURE REVIEWS CANCER, 2013, 13 (02) :97-110
[4]
Osteopontin promotes epithelial-mesenchymal transition of hepatocellular carcinoma through regulating vimentin [J].
Dong, Qiongzhu ;
Zhu, Xuchao ;
Dai, Chun ;
Zhang, Xiaofei ;
Gao, Xiaomei ;
Wei, Jinwang ;
Sheng, Yuanyuan ;
Zheng, Yan ;
Yu, Jian ;
Xie, Lu ;
Qin, Yi ;
Qiao, Peng ;
Zhou, Chuang ;
Yu, Xinxin ;
Jia, Huliang ;
Ren, Ning ;
Zhou, Haijun ;
Ye, Qinghai ;
Qin, Lunxiu .
ONCOTARGET, 2016, 7 (11) :12997-13012
[5]
Genetic variants in lncRNA H19 are associated with the risk of bladder cancer in a Chinese population [J].
Hua, Qiuhan ;
Lv, Xu ;
Gu, Xiang ;
Chen, Yaoyao ;
Chu, Haiyan ;
Du, Mulong ;
Gong, Weida ;
Wang, Meilin ;
Zhang, Zhengdong .
MUTAGENESIS, 2016, 31 (05) :531-538
[6]
AZD9291 in EGFR Inhibitor-Resistant Non-Small-Cell Lung Cancer [J].
Jaenne, Pasi A. ;
Yang, James Chih-Hsin ;
Kim, Dong-Wan ;
Planchard, David ;
Ohe, Yuichiro ;
Ramalingam, Suresh S. ;
Ahn, Myung-Ju ;
Kim, Sang-We ;
Su, Wu-Chou ;
Horn, Leora ;
Haggstrom, Daniel ;
Felip, Enriqueta ;
Kim, Joo-Hang ;
Frewer, Paul ;
Cantarini, Mireille ;
Brown, Kathryn H. ;
Dickinson, Paul A. ;
Ghiorghiu, Serban ;
Ranson, Malcolm .
NEW ENGLAND JOURNAL OF MEDICINE, 2015, 372 (18) :1689-1699
[7]
LncRNA HOTAIR promotes human liver cancer stem cell malignant growth through downregulation of SETD2 [J].
Li, Haiyan ;
An, Jiahui ;
Wu, Mengying ;
Zheng, Qidi ;
Gui, Xin ;
Li, Tianming ;
Pu, Hu ;
Lu, Dongdong .
ONCOTARGET, 2015, 6 (29) :27847-27864
[8]
Association of genetic variants in lncRNA H19 with risk of colorectal cancer in a Chinese population [J].
Li, Shuwei ;
Hua, Yibing ;
Jin, Jing ;
Wang, Haixiao ;
Du, Mulong ;
Zhu, Lingjun ;
Chu, Haiyan ;
Zhang, Zhengdong ;
Wang, Meilin .
ONCOTARGET, 2016, 7 (18) :25470-25477
[9]
Long non-coding RNA H19 promotes the proliferation and invasion of breast cancer through upregulating DNMT1 expression by sponging miR-152 [J].
Li, Zhen ;
Li, Yan ;
Li, Ya ;
Ren, Kewei ;
Li, Xin ;
Han, Xinwei ;
Wang, Jiaxiang .
JOURNAL OF BIOCHEMICAL AND MOLECULAR TOXICOLOGY, 2017, 31 (09)
[10]
The lncRNA H19 promotes epithelial to mesenchymal transition by functioning as miRNA sponges in colorectal cancer [J].
Liang, Wei-Cheng ;
Fu, Wei-Ming ;
Wong, Cheuk-Wa ;
Wang, Yan ;
Wang, Wei-Mao ;
Hu, Guo-Xin ;
Zhang, Li ;
Xiao, Li-Jia ;
Wan, David Chi-Cheong ;
Zhang, Jin-Fang ;
Waye, Mary Miu-Yee .
ONCOTARGET, 2015, 6 (26) :22513-22525