Chou Nan-Hua, Lo Yi-Hao, Wang Kuo-Chiang, Kang Chi-Hsiang, Tsai Chung-Yu, Tsai Kuo-Wang
Division of General Surgery, Department of Surgery, Kaohsiung Veterans General Hospital, Kaohsiung, Taiwan, R.O.C.
Department of Family Medicine, Zuoying Branch of Kaohsiung Armed Forces General Hospital, Kaohsiung, Taiwan, R.O.C.
Anticancer Res. 2018 Jun;38(6):3309-3318. doi: 10.21873/anticanres.12596.
BACKGROUND/AIM: MicroRNAs (miRNAs) are small non-protein-coding RNAs, that can be generated from the 5p or 3p arm of precursor miRNA (pre-miRNA). Differential miRNA arm selection has been reported between tumor and normal tissue in many cancer types; however, the biological function and mechanism of miRNA arm switching in gastric cancer remain unclear.
Profiles of miRNA expression in gastric cancer were obtained from The Cancer Genome Atlas (TCGA). The biological role of miR-193a-5p/-3p in tumor growth and invasive abilities was assessed through a gain-of-function approach. Target genes of miR-193a-3p were identified using bioinformatics and an experimental approach.
The expression levels of miR-193a-5p, and not of miR-193a-3p, were significantly decreased in gastric cancer compared to adjacent normal tissues. Ectopic expressions of miR-193a-5p and miR-193a-3p revealed that they both inhibited gastric cancer cell growth, but only miR-193a-3p significantly suppressed cell invasion ability. Using a bioinformatics approach, we identified 18 putative target genes of miR-193a-3p. Both mRNA and protein levels of cyclin D1 (CCND1) and ETS proto-oncogene 1 (ETS1) were significantly decreased in AGS cells transfected with miR-193a-3p mimics. ETS1 or CCND1 knockdown significantly suppressed gastric cancer cell growth, similar to miR-193a-3p overexpression.
Our results indicated that miR-193a-3p suppressed gastric growth and motility, at least partly, by directly targeting CCND1 and ETS1 expression.
背景/目的:微小RNA(miRNA)是一类小型非蛋白质编码RNA,可从前体miRNA(pre-miRNA)的5p或3p臂产生。在许多癌症类型中,肿瘤组织和正常组织之间存在miRNA臂选择差异;然而,胃癌中miRNA臂转换的生物学功能和机制仍不清楚。
从癌症基因组图谱(TCGA)获取胃癌中miRNA表达谱。通过功能获得性方法评估miR-193a-5p/-3p在肿瘤生长和侵袭能力方面的生物学作用。使用生物信息学和实验方法鉴定miR-193a-3p的靶基因。
与相邻正常组织相比,胃癌中miR-193a-5p的表达水平显著降低,而miR-193a-3p的表达水平未显著降低。miR-193a-5p和miR-193a-3p的异位表达表明它们均抑制胃癌细胞生长,但只有miR-193a-3p显著抑制细胞侵袭能力。使用生物信息学方法,我们鉴定出18个miR-193a-3p的假定靶基因。在用miR-193a-3p模拟物转染的AGS细胞中,细胞周期蛋白D1(CCND1)和ETS原癌基因1(ETS1)的mRNA和蛋白水平均显著降低。敲低ETS1或CCND1可显著抑制胃癌细胞生长,类似于miR-193a-3p过表达。
我们的结果表明,miR-193a-3p至少部分通过直接靶向CCND1和ETS1的表达来抑制胃癌的生长和迁移。