5-AMINOSALICYLIC ACID INHIBITS THE EXPRESSION OF ONCOmiRS AND PRO-INFLAMMATORY microRNAS: AN IN VITRO STUDY

被引:10
作者
Adamowicz, M. [1 ]
Milkiewicz, P. [2 ,3 ]
Kempinska-Podhorodecka, A. [1 ]
机构
[1] Pomeranian Med Univ, Dept Med Biol, Szczecin, Poland
[2] Med Univ Warsaw, Liver & Internal Med Unit, Warsaw, Poland
[3] Pomeranian Med Univ, Translat Med Grp, Szczecin, Poland
来源
JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY | 2021年 / 72卷 / 04期
关键词
ulcerative colitis; 5-aminosalicylic acid; microRNA; Caco-2 cell line; drug targets; microRNA pharmacogenomics; vitamin D receptor; Forkhead box O; DNA methyltransferase; NF-KAPPA-B; INFLAMED COLONIC-MUCOSA; ULCERATIVE-COLITIS; C-MYB; CELL DIFFERENTIATION; INTESTINAL BARRIER; DOWN-REGULATION; CANCER CELLS; VITAMIN-D; TRANSCRIPTION;
D O I
10.26402/jpp.2021.4.04
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
5-aminosalicylic acid (5-ASA) is commonly used as the first-line treatment for ulcerative colitis (UC). In this study, we show that the mechanism responsible for the protective effect of 5-ASA is associated with the modulation of non-coding microRNA molecule (miRNA) expression. Stimulation of human intestinal epithelial cells (Caco-2) with 1000 mu M of 5A-SA suppressed the levels of miR-125b, miR-150, miR-155, miR-346 and miR-506, which are known to be involved in the regulation of colitis and/or colorectal cancer in patients with inflammatory bowel disease. The 5-ASA-induced inhibitions of these miRNAs were associated with significant inductions of their target genes such as vitamin D receptor (VDR), suppressor of cytokine signaling (SOCS1), Forkhead box O (FOXO3a) and DNA methyltransferase 1 (DNMT1). The relationships between the selected miRNAs and their target genes were further confirmed in Caco-2 cells transfected of with specific miRNA inhibitors or miRNA mimics. Moreover, we showed that 5-ASA has the potential to hinder miR-155 expression induced by the transfection of miR-155 mimic into Caco-2 cells. These findings underline the anti-inflammatory and chemoprotective effects of 5-ASA treatment.
引用
收藏
页码:529 / 535
页数:7
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