Long non-coding RNA FEZF1-AS1 facilitates cell proliferation and migration in colorectal carcinoma

被引:100
|
作者
Chen, Na [1 ,2 ]
Guo, Dan [3 ]
Xu, Qiong [1 ,2 ]
Yang, Minhui [1 ,2 ]
Wang, Dan [1 ]
Peng, Man [1 ]
Ding, Yanqing [2 ]
Wang, Shuang [1 ,2 ]
Zhou, Jun [1 ,2 ]
机构
[1] Southern Med Univ, Nanfang Hosp, Dept Pathol, Guangzhou 510515, Guangdong, Peoples R China
[2] Southern Med Univ, Sch Basic Med Sci, Dept Pathol, Guangzhou 510515, Guangdong, Peoples R China
[3] Southern Med Univ, Nanfang Hosp, Dept Pharm, Guangzhou 510515, Guangdong, Peoples R China
关键词
FEZF1-AS1; FEZF1; colorectal cancer; long non-coding RNA; GASTRIC-CANCER; EXPRESSION; METASTASIS; PROMOTES; PROGNOSIS; MALAT1; SIGNATURE; APOPTOSIS; HOTAIR; LINKS;
D O I
10.18632/oncotarget.7168
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Long non-coding RNAs (lncRNA) have been shown to play important roles in the development and progression of cancer. Here, we discovered a novel long noncoding RNA (lncRNA) FEZF1 antisense RNA1 (FEZF1-AS1) is markedly upregulated in human primary colorectal carcinoma (CRC) and associated with CRC metastasis and poor prognosis. Moreover, the downregulation of FEZF1-AS1 expression significantly inhibited the CRC cells proliferation, migration and invasiveness, suppressed S-phase entry in vitro, and repressed tumor growth and metastasis in vivo. In contrast, overexpression of FEZF1-AS1 could promote the aggressive behaviors of CRC cells. We further discovered that the downregulation of FEZF1-AS1 reduced its sense-cognate gene FEZF1 mRNA and protein expression in CRC cells. There was a positive correlation between FEZF1-AS1 and FEZF1 expression in CRC. Moreover, FEZF1 knockdown also significantly suppressed CRC cell proliferation, migration, and invasion. Our findings indicate that the dysregulation of FEZF1-AS1 participates in colorectal tumorigenesis and progression, which might be achieved, at least in part, through FEZF1 induction.
引用
收藏
页码:11271 / 11283
页数:13
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