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miR-155 Down Regulation by LNA Inhibitor can Reduce Cell Growth and Proliferation in PC12 Cell Line

MicroRNAs (miRNAs) are a class of small non coding regulatory RNAs that have key functions in multiple cell processes. Deregulation of these tiny miRNAs is involved in various human diseases. MiR-155 is one of the multifunctional miRNA that its over-expression has been found to be associated with di...

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Autores principales: Kouhkan, Fatemeh, Alizadeh, Shaban, Kaviani, Saeid, Soleimani, Masoud, Pourfathollah, Ali Akbar, Amirizadeh, Naser, Abroun, Saeid, Noruzinia, Mehrdad, Mohamadi, Shahin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Avicenna Research Institute 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3558181/
https://www.ncbi.nlm.nih.gov/pubmed/23408179
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author Kouhkan, Fatemeh
Alizadeh, Shaban
Kaviani, Saeid
Soleimani, Masoud
Pourfathollah, Ali Akbar
Amirizadeh, Naser
Abroun, Saeid
Noruzinia, Mehrdad
Mohamadi, Shahin
author_facet Kouhkan, Fatemeh
Alizadeh, Shaban
Kaviani, Saeid
Soleimani, Masoud
Pourfathollah, Ali Akbar
Amirizadeh, Naser
Abroun, Saeid
Noruzinia, Mehrdad
Mohamadi, Shahin
author_sort Kouhkan, Fatemeh
collection PubMed
description MicroRNAs (miRNAs) are a class of small non coding regulatory RNAs that have key functions in multiple cell processes. Deregulation of these tiny miRNAs is 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.
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spelling pubmed-35581812013-02-13 miR-155 Down Regulation by LNA Inhibitor can Reduce Cell Growth and Proliferation in PC12 Cell Line Kouhkan, Fatemeh Alizadeh, Shaban Kaviani, Saeid Soleimani, Masoud Pourfathollah, Ali Akbar Amirizadeh, Naser Abroun, Saeid Noruzinia, Mehrdad Mohamadi, Shahin Avicenna J Med Biotechnol Original Article MicroRNAs (miRNAs) are a class of small non coding regulatory RNAs that have key functions in multiple cell processes. Deregulation of these tiny miRNAs is 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. Avicenna Research Institute 2011 /pmc/articles/PMC3558181/ /pubmed/23408179 Text en Copyright © 2011 Avicenna Research Institute http://creativecommons.org/licenses/by-nc/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly.
spellingShingle Original Article
Kouhkan, Fatemeh
Alizadeh, Shaban
Kaviani, Saeid
Soleimani, Masoud
Pourfathollah, Ali Akbar
Amirizadeh, Naser
Abroun, Saeid
Noruzinia, Mehrdad
Mohamadi, Shahin
miR-155 Down Regulation by LNA Inhibitor can Reduce Cell Growth and Proliferation in PC12 Cell Line
title miR-155 Down Regulation by LNA Inhibitor can Reduce Cell Growth and Proliferation in PC12 Cell Line
title_full miR-155 Down Regulation by LNA Inhibitor can Reduce Cell Growth and Proliferation in PC12 Cell Line
title_fullStr miR-155 Down Regulation by LNA Inhibitor can Reduce Cell Growth and Proliferation in PC12 Cell Line
title_full_unstemmed miR-155 Down Regulation by LNA Inhibitor can Reduce Cell Growth and Proliferation in PC12 Cell Line
title_short miR-155 Down Regulation by LNA Inhibitor can Reduce Cell Growth and Proliferation in PC12 Cell Line
title_sort mir-155 down regulation by lna inhibitor can reduce cell growth and proliferation in pc12 cell line
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3558181/
https://www.ncbi.nlm.nih.gov/pubmed/23408179
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