Li Shilei, Lv Chunyu, Li Jun, Xie Tao, Liu Xianbin, Zheng Zhiwei, Qin Zhaoyang, Hui Xizeng, Yu Yang
Department of General Surgery, Rizhao People's Hospital Rizhao 276800, Shandong, China.
Am J Transl Res. 2021 Jun 15;13(6):6066-6075. eCollection 2021.
Long noncoding RNAs (lncRNAs) have been shown to play crucial roles in cancer development. However, the role of LINC00473 in colorectal cancer has not been explored. In our study, we showed that LINC00473 expression was upregulated in colorectal cancer samples compared to nontumor samples. The expression of LINC00473 in colorectal cancer tissues from patients with distant metastasis was higher than that from cases without distant metastasis. The higher expression level of LINC00473 was positively correlated with advanced clinical stage. The elevated expression of LINC00473 accelerated colorectal cancer cell proliferation, cell cycle progression and invasion. Moreover, overexpression of LINC00473 induced epithelial to mesenchymal (EMT) progression in HT29 and SW480 cells. Ectopic expression of LINC00473 suppressed miR-195 expression in colorectal cancer cells. miR-195 expression was downregulated in colorectal cancer samples compared with nontumor samples. The expression of miR-195 in colorectal cancer tissues from patients with distant metastasis was lower than that from cases without distant metastasis. The lower expression level of miR-195 was positively correlated with advanced clinical stage. In addition, we showed that the expression of miR-195 was negatively correlated with the LINC00473 expression level in colorectal cancer tissues. LINC00473 accelerated colorectal cancer cell proliferation and cell cycle progression and regulated EMT progression by regulating miR-195 expression. These data suggested that LINC00473 induced cell proliferation, cell cycle progression and EMT progression by acting as a ceRNA for miR-195 in colorectal cancer.
长链非编码RNA(lncRNAs)已被证明在癌症发展中起关键作用。然而,LINC00473在结直肠癌中的作用尚未得到研究。在我们的研究中,我们发现与非肿瘤样本相比,LINC00473在结直肠癌样本中的表达上调。远处转移患者的结直肠癌组织中LINC00473的表达高于无远处转移患者的组织。LINC00473较高的表达水平与晚期临床分期呈正相关。LINC00473表达的升高加速了结直肠癌细胞的增殖、细胞周期进程和侵袭。此外,LINC00473的过表达诱导HT29和SW480细胞发生上皮-间质转化(EMT)进程。LINC00473的异位表达抑制了结直肠癌细胞中miR-195的表达。与非肿瘤样本相比,结直肠癌样本中miR-195的表达下调。远处转移患者的结直肠癌组织中miR-195的表达低于无远处转移患者的组织。miR-195较低的表达水平与晚期临床分期呈正相关。此外,我们发现结直肠癌组织中miR-195的表达与LINC00473的表达水平呈负相关。LINC00473通过调节miR-195的表达加速了结直肠癌细胞的增殖和细胞周期进程,并调节EMT进程。这些数据表明,在结直肠癌中,LINC00473作为miR-195的竞争性内源性RNA(ceRNA)诱导细胞增殖、细胞周期进程和EMT进程。