Lin Li, Gan Hua, Zhang Han, Tang Weixue, Sun Yue, Tang Xueqin, Kong Dequan, Zhou Jiajun, Wang Yuxuan, Zhu Yanlin
Department of Nephrology, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, P.R. China.
Department of Experiment Center, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, P.R. China.
Mol Med Rep. 2014 Aug;10(2):707-12. doi: 10.3892/mmr.2014.2312. Epub 2014 Jun 10.
MicroRNAs (miRNAs) are a class of small non‑coding single‑stranded RNAs that regulate gene expression at the posttranscriptional level. Since the identification of miRNA, accumulating research has shown their involvement in numerous biological processes, including timing of developmental patterning, embryogenesis, cell differentiation, organogenesis, growth control and pathogenesis of human diseases. It is estimated that >30% human genes may be regulated by miRNA, and that each miRNA can regulate >100 target mRNAs. The widespread and distinct expression pattern of miRNAs in normal and disease states has been extensively investigated in the context of human diseases. Due to the diversity of targets, it is challenging to identify the specific target genes and elucidate the biological function of a certain miRNAs. In the present study, it was confirmed that SMAD7 is a direct target of miR‑21, and overexpression of miR‑21 may inhibit the proliferation of rat renal tubular epithelial cells. These findings confirm the results of previous studies, which have demonstrated that miR‑21 regulates the expression of SMAD7 protein. However, further investigation is required to determine whether miR‑21 is involved in renal development and disease, particularly diabetic nephropathy.
微小RNA(miRNA)是一类小的非编码单链RNA,其在转录后水平调节基因表达。自miRNA被鉴定以来,越来越多的研究表明它们参与了众多生物学过程,包括发育模式的时间安排、胚胎发生、细胞分化、器官发生、生长控制以及人类疾病的发病机制。据估计,超过30%的人类基因可能受miRNA调控,并且每个miRNA可调控超过100个靶mRNA。在人类疾病背景下,miRNA在正常和疾病状态下广泛且独特的表达模式已得到广泛研究。由于靶标的多样性,鉴定特定靶基因并阐明某个miRNA的生物学功能具有挑战性。在本研究中,证实SMAD7是miR-21的直接靶标,并且miR-21的过表达可能抑制大鼠肾小管上皮细胞的增殖。这些发现证实了先前研究的结果,即miR-21调节SMAD7蛋白的表达。然而,需要进一步研究以确定miR-21是否参与肾脏发育和疾病,特别是糖尿病肾病。