CTGF公司
基因敲除
生物
结直肠癌
生长因子
癌症研究
结缔组织
细胞生长
小发夹RNA
下调和上调
信使核糖核酸
细胞
细胞培养
分子生物学
癌症
受体
遗传学
基因
作者
Weijian Lun,Xiaobin Zhang,Yinsheng Hong,Canhua Luo,Yongjia Liu
出处
期刊:Epigenomics
[Future Medicine]
日期:2024-07-17
卷期号:16 (14): 985-998
被引量:1
标识
DOI:10.1080/17501911.2024.2373686
摘要
Aim: This study aimed to investigate the role of LINC00513 in colorectal cancer (CRC) progression. Materials & methods: Cell proliferation was evaluated using Cell Counting Kit-8. Cell migration was detected with transwell assay. RNA pull-down was applied for verifying the interactions between LINC00513, IGF2BP1 and connective tissue growth factor (CTGF). Results: LINC00513, IGF2BP1 and CTGF levels were upregulated in CRC. Knockdown of LINC00513 significantly inhibited the malignant behavior of CRC cells. LINC00513 increased CTGF mRNA stability by binding with IGF2BP1. Furthermore, overexpression of IGF2BP1 or CTGF reversed the inhibitory effect of LINC00513 shRNA on CRC progression. Conclusion: LINC00513 promoted CRC cell malignant behaviors through IGF2BP1/CTGF.
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