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, IGF2BP1Â and connective tissue growth factor (CTGF).Results: LINC00513, IGF2BP1Â 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.
LINC00513 promotes colorectal cancer malignant progression by binding with IGF2BP1 to enhance the stability of connective tissue growth factor mRNA.
LINC00513 通过与 IGF2BP1 结合,增强结缔组织生长因子 mRNA 的稳定性,从而促进结直肠癌的恶性进展
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作者:Lun Weijian, Zhang Xiaobin, Hong Yinsheng, Luo Canhua, Liu Yongjia
| 期刊: | Epigenomics | 影响因子: | 2.600 |
| 时间: | 2024 | 起止号: | 2024;16(14):985-998 |
| doi: | 10.1080/17501911.2024.2373686 | 研究方向: | 肿瘤 |
| 疾病类型: | 肠癌 | ||
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