High Expression of the Newly Found Long Noncoding RNA Z38 Promotes Cell Proliferation and Oncogenic Activity in Breast Cancer

被引:37
作者
Deng, Rilin [1 ]
Liu, Bin [1 ]
Wang, Yan [2 ]
Yan, Feng [3 ]
Hu, Shifan [1 ]
Wang, Hongcan [1 ]
Wang, Tingting [1 ]
Li, Bin [1 ]
Deng, Xiyun [4 ]
Xiang, Shuanglin [3 ]
Yang, Yinke [1 ]
Zhang, Jian [1 ]
机构
[1] Hunan Univ, Coll Biol, Changsha 410082, Hunan, Peoples R China
[2] Zunyi Med Coll, Dept Biol Engn, Zhuhai Campus, Zhuhai 519041, Guangdong, Peoples R China
[3] Hunan Normal Univ, Coll Life Sci, Changsha 410000, Hunan, Peoples R China
[4] Hunan Normal Univ, Coll Med, Fac Basic Med Sci, Changsha 410013, Hunan, Peoples R China
关键词
lncRNA Z38; CLDND1; cell proliferation; tumorigenesis; oncogene; siRNA; GENE; CLAUDINS; GROWTH; MECHANISMS; CHROMATIN; RISK;
D O I
10.7150/jca.13117
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The aberrant expression of long noncoding RNAs (lncRNAs) has great impacts on cancer origination and progression. In the current study, a newly found lncRNA Z38, which was identified through combining experiments of suppression subtractive hybridization (SSH) and reverse dot-blotting, was found to have high expression in breast cancer. More importantly, inhibiting Z38 expression by gene silencing greatly suppressed breast cancer cell proliferation and tumorigenesis, and treatment with Z38 siRNAs significantly induced cell apoptosis and inhibited tumor growth. In conclusion, the newly found lncRNA Z38, which plays important roles in breast cancer, may act as a candidate biomarker and therapeutic target in carcinomas.
引用
收藏
页码:576 / 586
页数:11
相关论文
共 51 条
[21]   Noncoding RNA Gas5 Is a Growth Arrest- and Starvation-Associated Repressor of the Glucocorticoid Receptor [J].
Kino, Tomoshige ;
Hurt, Darrell E. ;
Ichijo, Takamasa ;
Nader, Nancy ;
Chrousos, George P. .
SCIENCE SIGNALING, 2010, 3 (107) :ra8
[22]   The claudins [J].
Lal-Nag, Madhu ;
Morin, Patrice J. .
GENOME BIOLOGY, 2009, 10 (08) :235
[23]   Physiological roles of long noncoding RNAs: insight from knockout mice [J].
Li, Lingjie ;
Chang, Howard Y. .
TRENDS IN CELL BIOLOGY, 2014, 24 (10) :594-602
[24]   A Cytoplasmic NF-κB Interacting Long Noncoding RNA Blocks IκB Phosphorylation and Suppresses Breast Cancer Metastasis [J].
Liu, Bodu ;
Sun, Lijuan ;
Liu, Qiang ;
Gong, Chang ;
Yao, Yandan ;
Lv, Xiaobin ;
Lin, Ling ;
Yao, Herui ;
Su, Fengxi ;
Li, Dangsheng ;
Zeng, Musheng ;
Song, Erwei .
CANCER CELL, 2015, 27 (03) :370-381
[25]   Forkhead box C1 promoter upstream transcript, a novel long non-coding RNA, regulates proliferation and migration in basal-like breast cancer [J].
Liu, Juntao ;
Shen, Lei ;
Yao, Jie ;
Li, Yi ;
Wang, Yongcheng ;
Chen, Hong ;
Geng, Peiliang .
MOLECULAR MEDICINE REPORTS, 2015, 11 (04) :3155-3159
[26]   The lncRNA PCAT29 Inhibits Oncogenic Phenotypes in Prostate Cancer [J].
Malik, Rohit ;
Patel, Lalit ;
Prensner, John R. ;
Shi, Yang ;
Iyer, Matthew K. ;
Subramaniyan, Shruthi ;
Carley, Alexander ;
Niknafs, Yashar S. ;
Sahu, Anirban ;
Han, Sumin ;
Ma, Teng ;
Liu, Meilan ;
Asangani, Irfan A. ;
Jing, Xiaojun ;
Cao, Xuhong ;
Dhanasekaran, Saravana M. ;
Robinson, Dan R. ;
Feng, Felix Y. ;
Chinnaiyan, Arul M. .
MOLECULAR CANCER RESEARCH, 2014, 12 (08) :1081-1087
[27]  
Matheis Fanny, 2014, Methods Mol Biol, V1169, P181, DOI 10.1007/978-1-4939-0882-0_17
[28]   Predicted expansion of the claudin multigene family [J].
Mineta, Katsuhiko ;
Yamamoto, Yasuko ;
Yamazaki, Yuji ;
Tanaka, Hiroo ;
Tada, Yukiyo ;
Saito, Kuniaki ;
Tamura, Atsushi ;
Igarashi, Michihiro ;
Endo, Toshinori ;
Takeuchi, Kosei ;
Tsukita, Sachiko .
FEBS LETTERS, 2011, 585 (04) :606-612
[29]   Claudin proteins in human cancer: Promising new targets for diagnosis and therapy [J].
Morin, PJ .
CANCER RESEARCH, 2005, 65 (21) :9603-9606
[30]   Long Noncoding RNA ANRIL Promotes Non-Small Cell Lung Cancer Cell Proliferation and Inhibits Apoptosis by Silencing KLF2 and P21 Expression [J].
Nie, Feng-qi ;
Sun, Ming ;
Yang, Jin-song ;
Xie, Min ;
Xu, Tong-peng ;
Xia, Rui ;
Liu, Yan-wen ;
Liu, Xiang-hua ;
Zhang, Er-bao ;
Lu, Kai-hua ;
Shu, Yong-qian .
MOLECULAR CANCER THERAPEUTICS, 2015, 14 (01) :268-277