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Cell Type-Dependent Functions of Microrna-92A Publisher Pubmed



Kohram F1, 2, 3 ; Fallah P2, 4 ; Shamsara M5 ; Bolandi Z6 ; Rassoulzadegan M7 ; Soleimani M8 ; Ghanbarian H1, 6
Authors
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Authors Affiliations
  1. 1. Cellular and Molecular Biology Research Center, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  2. 2. Department of Molecular Biology and Genetic Engineering, Stem Cell Technology Research Center, Tehran, Iran
  3. 3. Department of Cell, Molecular, and Structural Biology, Miami University, Oxford, OH, United States
  4. 4. Faculty of Para-Medicine, Medical Laboratory Sciences Department, Alborz University of Medical Sciences, Karaj, Iran
  5. 5. Animal Biotechnology Department, National Institute of Genetic Engineering and Biotechnology, Tehran, Iran
  6. 6. Department of Biotechnology, School of Advanced Technologies in Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  7. 7. Universite Cote d'Azur, CNRS, INSERM, iBV, Nice, France
  8. 8. Faculty of Medical Science, Department of Hematology, Tarbiat Modares University, Tehran, Iran

Source: Journal of Cellular Biochemistry Published:2018


Abstract

The role of miR-17/92 family in development and progression of various cancers has been established. The members of this miRNA family have been shown to be over expressed and target various genes within proliferation, metastasis and angiogenesis pathways. Although all members might be overexpressed in a certain cancer type, only certain members of the family may have roles in progression of that cancer. In this study, we have chosen miR-92a, a member of the miR-17/92 family to compare its function in three different cancer cell lines. HL60, MCF7, and Jurkat cell lines were transduced with miR-92a and proliferation and apoptosis was measured in these cells by cell count, MTT, and caspase assays. Although in comparison to pre-miR-17/92, the level of miR-92a is higher in Jurkat cells compared to MCF7 and HL60 cells, here we have shown that increasing miR-92a levels results in apoptosis in Jurkat cells and proliferation in MCF7 and HL60 cells. miR-92a was also microinjected into mice fertilized eggs and after dissection, apoptosis was only observed in white pulp of spleen that is mainly made up of white blood cells. Our results show that miR-92a possesses a cell-type dependent function. © 2018 Wiley Periodicals, Inc.