Title of article
miR-155 Down Regulation by LNA Inhibitor can Reduce Cell Growth and Proliferation in PC12 Cell Line
Author/Authors
Kouhkan، Fatemeh نويسنده Department of Genetics, Faculty of Basic Sciences, Tarbiat Modares University , , Alizadeh، Shaban Ali نويسنده Department of Surgery, School of Medicine, Arak University of Medical Sciences, Arak, Iran , , Kaviani، Saeid نويسنده , , Soleimani، Masoud نويسنده , , Pourfathollah، Ali Akbar نويسنده , , Amirizadeh، Naser نويسنده , , Abroun، Saeid نويسنده Hematology Department, School of Medical Sciences, Tarbiat Modares University, Tehran, Iran , , Noruzinia، Mehrdad نويسنده , , Mohamadi، Shahin نويسنده Department of Hematology, Allied Medical School, Tehran University of Medical Sciences ,
Issue Information
فصلنامه با شماره پیاپی 9 سال 2011
Pages
6
From page
61
To page
66
Abstract
MicroRNAs (miRNAs) are a class of small non coding regulatory RNAs that have key functions in multiple cell processes. Deregulation of these tiny miRNAs are involved in various human diseases. MiR-155 is one of the multifunctional miRNA that its over-expression has been found to be associated with different kinds of cancer such as leukemia, breast and colon cancers. It is thought that deregulation and over-expression of this microRNA may be associated with PC12 cell proliferation. So, the aim of this study was to investigate the role of miR-155 expression on PC12 cell growth. For this reason, PC12 cells were cultured and transfected by 3 different concentration (25, 50 and 75 nmol) of either LNA anti-miR-155 or scramble antisense in 24-well plate. Then, total RNA was extracted from transfected cells. miRNA cDNAs were synthesized from isolated total RNA. In the second step, miR-155 expression level was analyzed using the quantitative real-time polymerase chain reaction (QRT-PCR). MTT test was performed to evaluate cell viability. In the next step, apoptosis assay was assessed to investigate anti miR-155 effect on PC12 cells death. Obtained results were analyzed with t-test. MTT test revealed that cell viability of transfected cells with 75 nM of anti-miR- 155 to be reduced by half of the control and scramble groups (0.5 vs. 0.97 and 0.94). Our data suggest that miR-155 over-expression is associated with PC12 cell growth. So, miR-155 down regulation by anti-miR-155 could open up new ways to restrain brain tumor growth, as anti-miR-155 causes PC12 cells to repress.
Journal title
AJMB Avicenna Journal of Medical Biotechnology
Serial Year
2011
Journal title
AJMB Avicenna Journal of Medical Biotechnology
Record number
1982807
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