Zhao Changjie, Jiang Qi, Chen Lin, Chen Wei
Endoscopy Center, Affiliated Dongtai Hospital of Nantong University, Dongtai, Jiangsu 224200, P.R. China.
Department of Gastroenterology, Affiliated Dongtai Hospital of Nantong University, Dongtai, Jiangsu 224200, P.R. China.
Exp Ther Med. 2021 Jul;22(1):685. doi: 10.3892/etm.2021.10117. Epub 2021 Apr 26.
Colorectal cancer (CRC) is one of the most common human cancer types and a leading cause of cancer-related death. Accumulating evidence has confirmed that long non-coding RNAs have crucial roles in CRC progression. In the present study, the biological roles of LINC01535 were investigated and the interaction between long intergenic non-coding RNA (LINC)01535 and microRNA (miR)-761 in CRC was explored. LINC01535 expression was observed to be upregulated in CRC tissues and cell lines. A functional study suggested that LINC01535 silencing inhibited CRC cell proliferation and invasion but enhanced cisplatin sensitivity of CRC cells, while co-transfection with a miR-761 inhibitor reversed these biological effects. A luciferase reporter assay demonstrated that LINC01535 regulated miR-761 directly and RNA-binding protein immunoprecipitation further confirmed that the suppression of LINC01535 by miR-761 was via an RNA-induced silencing complex. Finally, knockdown of LINC01535 inhibited the growth of CRC cells . Collectively, the results suggested that LINC01535 exerts oncogenic functions in CRC by sponging miR-761. In conclusion, the present study indicated that LINC01535 promoted CRC progression through sponging miR-761, and may serve as a potential diagnostic biomarker and therapeutic target for CRC.
结直肠癌(CRC)是人类最常见的癌症类型之一,也是癌症相关死亡的主要原因。越来越多的证据证实,长链非编码RNA在CRC进展中起关键作用。在本研究中,我们研究了LINC01535的生物学作用,并探讨了长链基因间非编码RNA(LINC)01535与微小RNA(miR)-761在CRC中的相互作用。观察到LINC01535在CRC组织和细胞系中表达上调。功能研究表明,LINC01535沉默可抑制CRC细胞增殖和侵袭,但增强CRC细胞对顺铂的敏感性,而与miR-761抑制剂共转染可逆转这些生物学效应。荧光素酶报告基因检测表明LINC01535直接调控miR-761,RNA结合蛋白免疫沉淀进一步证实miR-761对LINC01535的抑制是通过RNA诱导沉默复合体实现的。最后,敲低LINC01535可抑制CRC细胞生长。总体而言,结果表明LINC01535通过海绵吸附miR-761在CRC中发挥致癌作用。总之,本研究表明LINC01535通过海绵吸附miR-761促进CRC进展,可能作为CRC潜在的诊断生物标志物和治疗靶点。