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微小RNA-140-5p通过靶向血管内皮生长因子A抑制结直肠癌的进展。

MicroRNA-140-5p inhibits the progression of colorectal cancer by targeting VEGFA.

作者信息

Zhang Wenbo, Zou Chen, Pan Lei, Xu Ying, Qi Weidong, Ma Gui, Hou Yongzhong, Jiang Pengcheng

出版信息

Cell Physiol Biochem. 2015;37(3):1123-33. doi: 10.1159/000430237. Epub 2015 Sep 25.

Abstract

BACKGROUND

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.

METHODS

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.

RESULTS

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.

CONCLUSIONS

Our results suggested a tumor suppressive role of miR-140-5p in CRC tumorigenesis and progression by targeting VEGFA.

摘要

背景

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。

方法

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。

结果

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。

结论

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。

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