MiR-340-5p is a potential prognostic indicator of colorectal cancer and modulates ANXA3

被引:6
|
作者
Yang, L. [1 ]
Men, W-L [2 ]
Yan, K-M [3 ]
Tie, J. [4 ,5 ]
Nie, Y-Z [4 ,5 ]
Xiao, H-J [3 ,4 ,5 ]
机构
[1] Xianyang Cent Hosp, Dept Gen Surg, Xianyang, Shaanxi, Peoples R China
[2] Chinese Acad Engn, Consultancy Program Ctr, Project Dept, Beijing, Peoples R China
[3] Shaanxi Univ Chinese Med, Affiliated Hosp, Dept Oncol, Xianyang, Shaanxi, Peoples R China
[4] Fourth Mil Med Univ, Natl Clin Res Ctr Digest Dis, State Key Lab Canc Biol, Xian, Shaanxi, Peoples R China
[5] Fourth Mil Med Univ, Xing Hosp Digest Dis, Xian, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
miR-340-5p; Annexin A3; Proliferation; Migration; Invasion; Colorectal cancer; Prognosis; CELL-PROLIFERATION; TUMOR-SUPPRESSOR; ANNEXIN A3; METASTASIS; GROWTH; APOPTOSIS; EXPRESSION; SURVIVAL;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
OBJECTIVE: MicroRNAs (miRNAs) are increasingly recognized as oncogenes or tumor suppressors in colorectal cancer (CRC). The aim of this study was to explore the expression and functions of miR-340-5p in CRC. PATIENTS AND METHODS: The expression of miR-340-5p in CRC tissues and cell lines was detected by quantitative RT-PCR. Associations of miR-340-5p expression with clinicopathological factors and overall survival (OS) and progression-free survival (PFS) were statistically evaluated. Luciferase assay, RT-PCR, and Western blot were performed to verify the precise target of miR-340-5p. MTT assay, colony formation and transwell assay were performed to determine the proliferation, migration and invasion, respectively. RESULTS: Our results showed that miR-340-5p was significantly down-regulated in CRC tissues and cell lines, and was associated with histological grade (p=0.020), lymph nodes metastasis (p=0.003) and TNM stage (p=0.007). Furthermore, Kaplan-Meier and log-rank tests revealed that patients with low expression of miR-340-5p had a shorter OS (p=0.0110) and PFS (p=0.0032) than those with high expression of miR-340-5p. We further validated Annexin A3 (ANXA3) was a direct target of miR-340-5p in CRC. The functional assay showed that up-regulation of miR-340-5p or down-regulation of ANXA3 can both inhibit CRC cell proliferation, migration, and invasion. Besides, the re-expression of ANXA3 reversed the miR-340-5p induced suppression of cell proliferation, migration and invasion. CONCLUSIONS: Our data demonstrated that miR-340-5p exerted its tumor-suppressive function by directly targeting ANXA3 in CRC, suggesting that miR-340-5p might represent a novel prognostic biomarker and therapeutic target for CRC.
引用
收藏
页码:4837 / 4845
页数:9
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