Zhang Wenbo, Zou Chen, Pan Lei, Xu Ying, Qi Weidong, Ma Gui, Hou Yongzhong, Jiang Pengcheng
Cell Physiol Biochem. 2015;37(3):1123-33. doi: 10.1159/000430237. Epub 2015 Sep 25.
microRNAs (miRNAs) are small non-coding RNAs and have been shown to play a crucial role in the colorectal cancer (CRC) tumorigenesis and progression. The aim of this study was to investigate the clinical significance and prognostic value of miR-140-5p in CRC. The exact functions and the underlying molecular mechanisms of miR-140-5p in CRC was further determined.
miR-140-5p expression was detected in CRC samples, their adjacent nontumor tissues as well as CRC cell lines by RT-qPCR. Cell proliferation was detected using CCK-8, and cell invasion and migration were evaluated using Transwell assay. The direct regulation of VEGFA by miR-140-5p was identified using luciferase reporter assay.
miR-140-5p was significantly dowregulated in CRC tissues and cell lines. Downregulation of miR-140-5p was significantly correlated with advanced CRC stage and poorer overall survival. Both gain-of-function and loss of function studies demonstrated that miR-140-5p acted as a tumor suppressor by inhibiting cell proliferation, migration and invasion. Integrated analysis identified VEGFA as a direct and functional target gene of miR-140-5p. Silencing VEGFA by small interfering RNA (siRNA) resembled the phenotype resulting from ectopic miR-140-5p expression, while overexpression of VEGFA attenuated the effect of miR-140-5p on CRC cells.
Our results suggested a tumor suppressive role of miR-140-5p in CRC tumorigenesis and progression by targeting VEGFA.
微小RNA(miRNA)是一类小的非编码RNA,已被证明在结直肠癌(CRC)的肿瘤发生和进展中起关键作用。本研究旨在探讨miR-140-5p在CRC中的临床意义和预后价值。进一步确定了miR-140-5p在CRC中的具体功能和潜在分子机制。
采用逆转录定量聚合酶链反应(RT-qPCR)检测CRC样本、其相邻的非肿瘤组织以及CRC细胞系中miR-140-5p的表达。使用细胞计数试剂盒-8(CCK-8)检测细胞增殖,并使用Transwell实验评估细胞侵袭和迁移能力。通过荧光素酶报告基因实验确定miR-140-5p对血管内皮生长因子A(VEGFA)的直接调控作用。
miR-140-5p在CRC组织和细胞系中显著下调。miR-140-5p的下调与晚期CRC分期及较差的总生存期显著相关。功能获得和功能丧失研究均表明,miR-140-5p通过抑制细胞增殖、迁移和侵袭发挥肿瘤抑制作用。综合分析确定VEGFA是miR-140-5p的直接功能靶基因。通过小干扰RNA(siRNA)沉默VEGFA产生的表型与异位表达miR-140-5p相似,而VEGFA的过表达减弱了miR-140-5p对CRC细胞的作用。
我们的结果表明,miR-140-5p通过靶向VEGFA在CRC的肿瘤发生和进展中发挥肿瘤抑制作用。