Title of article :
Restoration of miRNA-143 Expression Inhibits Growth and Migration of MKN-45 Gastric Cancer Cell Line
Author/Authors :
Hosseinahli ، Nayer Immunology Research Center - Tabriz University of Medical Sciences , Zeinali ، Tahereh Immunology Research Center - Tabriz University of Medical Sciences , Hosseinahli ، Nasrin Azarbaijan Higher Education and Research Complex , Karimi ، Leila Immunology Research Center - Tabriz University of Medical Sciences , Shanehbandi ، Dariush , Mansoori ، Behzad , Mohammadi ، Ali Immunology Research Center - Tabriz University of Medical Sciences , Kazemi ، Tohid Department of Immunology - Tabriz University of Medical Sciences , Hajiasgharzadeh ، Khalil Connective Tissue Diseases Research Center, Immunology Research Center - Tabriz University of Medical Sciences , Baradaran ، Behzad
From page :
183
To page :
190
Abstract :
Purpose: Gastric cancer (GC) is one of the main causes of death from diseases, especially in developing countries. MicroRNAs (miRNAs) are important modulators of the messenger RNAs expression. Among these miRNAs, MiR-143 is a tumor suppressor miRNA and its irregular expression has been revealed in a diversity of malignancies such as GC. Methods: In this study, we have attempted to restore the miR-143 expression in MKN-45 cells by introducing pCMV-miR-143 plasmid vectors. The consequences of exogenous expression of miR-143 on cell proliferation and migration were assessed by MTT and scratch tests, respectively. In addition, the DAPI staining assay was applied for apoptosis quantification. Following miR- 143 transfection, the changes in K-Ras, C-Myc, MMP9, Bax, caspase-3, and caspase-9 mRNA levels were assessed. Results: The results indicated that the enhanced expression of miR-143 had negative effects on MKN-45 cells proliferation and invasion. Moreover, decreased expressions of K-Ras, MMP9, and C-Myc and up-regulation of Bax, caspase-3, and caspase-9 as downstream targets of miR- 143 were recognized. Conclusion: These experimental results indicate that reversing the miR-143 expression, by novel techniques, including miRNA replacement could be considered as an efficient approach to reduce cell survival and metastasis.
Keywords :
Gastric Cancer , miR , 143 , Replacement Therapy , Proliferation , Apoptosis , Migration Ability
Journal title :
Advanced Pharmaceutical Bulletin
Journal title :
Advanced Pharmaceutical Bulletin
Record number :
2719743
Link To Document :
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