Wu Yuanyu, Wan Xiaoyu, Zhao Xin, Song Zheyu, Xu Zhonghang, Tao Youmao, Sun Caixia
Department of Gastrointestinal Colorectal and Anal Surgery, China-Japan Union Hospital, Jilin University Changchun 130033, Jilin, China.
Department of Tumor Surgery, Jilin University Second Hospital Changchun 130000, Jilin, China.
Am J Transl Res. 2020 Mar 15;12(3):867-874. eCollection 2020.
Accumulating evidences suggest that miRNAs may prove essential therapeutic targets for the treatment of cancer. Herein, the role and therapeutic implications of miRNA-143 was investigated in gastric cancer. The results revealed miRNA-143 to be aberrantly downregulated in gastric cancer cell lines. Ectopic expression of miRNA-143 resulted in a significant (<0.05) inhibition of AGS gastric cancer cell proliferation suggestive of the tumor suppressive role of miRNA-143. The inhibition of AGS cell proliferation was mainly via activation of apoptotic cell death as evident from the AO/EB and annexin V/PI staining. Additionally, miR-143 overexpression also caused a significant (<0.05) decline in the migration and invasion of AGS cells. TargetScan analysis and the dual luciferase assay revealed STAT3 to be the potential target of miRNA-143 in AGS cells. Analysis of STAT3 expression in gastric cancer cell lines showed upto 3.5 fold upregulation of STAT3. However, miRNA-143 overexpression resulted in considerable downregulation of STAT3 expression. Silencing of STAT3 also resulted in the inhibition of cell proliferation, migration and invasion of the AGS cells. Moreover, overexpression of STAT3 could nullify the tumor suppressive effects of miRNA-143 in AGS cells. Taken together, miRNA-143 has a tumor suppressive role in gastric cancer and may prove essential in gastric cancer treatment.
越来越多的证据表明,微小RNA(miRNA)可能是治疗癌症的关键治疗靶点。在此,我们研究了miRNA - 143在胃癌中的作用及其治疗意义。结果显示,miRNA - 143在胃癌细胞系中异常下调。miRNA - 143的异位表达导致AGS胃癌细胞增殖受到显著抑制(<0.05),提示miRNA - 143具有肿瘤抑制作用。从AO/EB和膜联蛋白V/PI染色可以明显看出,AGS细胞增殖的抑制主要是通过激活凋亡性细胞死亡实现的。此外,miR - 143的过表达还导致AGS细胞的迁移和侵袭能力显著下降(<0.05)。TargetScan分析和双荧光素酶测定显示,STAT3是miRNA - 143在AGS细胞中的潜在靶点。对胃癌细胞系中STAT3表达的分析表明,STAT3的表达上调了高达3.5倍。然而,miRNA - 143的过表达导致STAT3表达显著下调。STAT3的沉默也导致AGS细胞的增殖、迁移和侵袭受到抑制。此外,STAT3的过表达可以消除miRNA - 143在AGS细胞中的肿瘤抑制作用。综上所述,miRNA - 143在胃癌中具有肿瘤抑制作用,可能在胃癌治疗中发挥重要作用。