Circular RNA 0000096 affects cell growth and migration in gastric cancer

被引:227
作者
Li, Peifei [1 ,3 ]
Chen, Huilin [2 ]
Chen, Shengcan [1 ]
Mo, Xiaoyan [1 ]
Li, Tianwen [1 ]
Xiao, Bingxiu [1 ]
Yu, Rui [1 ]
Guo, Junming [1 ]
机构
[1] Ningbo Univ, Dept Biochem & Mol Biol, Zhejiang Key Lab Pathophysiol, Sch Med, Ningbo 315211, Zhejiang, Peoples R China
[2] Ningbo Coll Hlth Sci, Dept Human Body Funct, Ningbo 315010, Zhejiang, Peoples R China
[3] Ningbo First Hosp, Dept Gastroenterol, 59 Liuting St, Ningbo 315010, Zhejiang, Peoples R China
关键词
cell growth; gastric cancer; molecular carcinogenesis; RNA expression; BREAST-CANCER; MESSENGER-RNAS; GENE; EXON; EXPRESSION; TRANSCRIPTS; DATABASE; PTEN;
D O I
10.1038/bjc.2016.451
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Circular RNAs (circRNAs) are a class of non-coding RNAs broadly expressed in cells of various species. Their role in cancers, especially in gastric cancer, is poorly understood. Methods: Circular RNA 0000096 (hsa_circ_0000096) levels in 101 paired gastric cancer tissues and adjacent non-tumorous tissues from patients with gastric cancer were detected by real-time quantitative reverse transcription-polymerase chain reaction. A receiver operating characteristic curve was generated to evaluate the diagnostic value of hsa_circ_0000096. RNA interference was used to manipulate the expression of hsa_circ_0000096. Its biological effects were evaluated by flow cytometry, real-time cell analysis, a wound scratch assay, western blot analysis and xenograft models. Results: Hsa_circ_0000096 was found to be significantly downregulated in gastric cancer tissues and gastric cancer cell lines compared with paired adjacent non-tumorous tissues and normal gastric epithelial cells (P<0.001). Moreover, knockdown of hsa_circ_0000096 significantly inhibited cell proliferation and migration in vitro and in vivo. The results of both immunohistochemical and western blot analyses showed that the protein levels of cyclin D1, cyclin-dependent kinase 6 (CDK6), matrix metalloproteinase-2 and MMP-9 were significantly reduced in vitro and in vivo. A gastric cancer xenograft nude mouse model indicated that Ki67 and VEGF were reduced in a dose-dependent manner following knockdown of hsa_circ_0000096. However, the expression of E-cadherin increased. Conclusions: Hsa_circ_0000096 may be used as a potential novel biomarker for gastric cancer. It affects gastric cancer cell growth and migration by regulating cyclin D1, CDK6, MMP-2 and MMP-9.
引用
收藏
页码:626 / 633
页数:8
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