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Non-coding RNAs change their expression profile after Retinoid induced differentiation of the promyelocytic cell line NB4
BACKGROUND: The importance of non-coding RNAs (ncRNAs) as fine regulators of eukaryotic gene expression has emerged by several studies focusing on microRNAs (miRNAs). miRNAs represent a newly discovered family of non coding-RNAs. They are thought to be crucial players of human hematopoiesis and rela...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2843733/ https://www.ncbi.nlm.nih.gov/pubmed/20181027 http://dx.doi.org/10.1186/1756-0500-3-24 |
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author | Rossi, Annalisa D'Urso, Oscar F Gatto, Graziana Poltronieri, Palmiro Ferracin, Manuela Remondelli, Paolo Negrini, Massimo Caporaso, Maria G Bonatti, Stefano Mallardo, Massimo |
author_facet | Rossi, Annalisa D'Urso, Oscar F Gatto, Graziana Poltronieri, Palmiro Ferracin, Manuela Remondelli, Paolo Negrini, Massimo Caporaso, Maria G Bonatti, Stefano Mallardo, Massimo |
author_sort | Rossi, Annalisa |
collection | PubMed |
description | BACKGROUND: The importance of non-coding RNAs (ncRNAs) as fine regulators of eukaryotic gene expression has emerged by several studies focusing on microRNAs (miRNAs). miRNAs represent a newly discovered family of non coding-RNAs. They are thought to be crucial players of human hematopoiesis and related tumorigenesis and to represent a potential tool to detect the early stages of cancer. More recently, the expression regulation of numerous long ncRNAs has been linked to cell growth, differentiation and cancer although the molecular mechanism of their function is still unknown. NB4 cells are promyelocytic cells that can be induced to differentiation upon retinoic acid (ATRA) treatment and represent a feasible model to study changes of non coding RNAs expression between cancer cells and their terminally differentiated counterpart. FINDINGS: we screened, by microarray analysis, the expression of 243 miRNAs and 492 human genes transcribing for putative long ncRNAs different from miRNAs in NB4 cells before and after ATRA induced differentiation. Our data show that 8 miRNAs, and 58 long ncRNAs were deregulated by ATRA induced NB4 differentiation. CONCLUSION: our data suggest that ATRA-induced differentiation lead to deregulation of a large number of the ncRNAs that can play regulatory roles in both tumorigenesis and differentiation. |
format | Text |
id | pubmed-2843733 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-28437332010-03-23 Non-coding RNAs change their expression profile after Retinoid induced differentiation of the promyelocytic cell line NB4 Rossi, Annalisa D'Urso, Oscar F Gatto, Graziana Poltronieri, Palmiro Ferracin, Manuela Remondelli, Paolo Negrini, Massimo Caporaso, Maria G Bonatti, Stefano Mallardo, Massimo BMC Res Notes Short Report BACKGROUND: The importance of non-coding RNAs (ncRNAs) as fine regulators of eukaryotic gene expression has emerged by several studies focusing on microRNAs (miRNAs). miRNAs represent a newly discovered family of non coding-RNAs. They are thought to be crucial players of human hematopoiesis and related tumorigenesis and to represent a potential tool to detect the early stages of cancer. More recently, the expression regulation of numerous long ncRNAs has been linked to cell growth, differentiation and cancer although the molecular mechanism of their function is still unknown. NB4 cells are promyelocytic cells that can be induced to differentiation upon retinoic acid (ATRA) treatment and represent a feasible model to study changes of non coding RNAs expression between cancer cells and their terminally differentiated counterpart. FINDINGS: we screened, by microarray analysis, the expression of 243 miRNAs and 492 human genes transcribing for putative long ncRNAs different from miRNAs in NB4 cells before and after ATRA induced differentiation. Our data show that 8 miRNAs, and 58 long ncRNAs were deregulated by ATRA induced NB4 differentiation. CONCLUSION: our data suggest that ATRA-induced differentiation lead to deregulation of a large number of the ncRNAs that can play regulatory roles in both tumorigenesis and differentiation. BioMed Central 2010-01-27 /pmc/articles/PMC2843733/ /pubmed/20181027 http://dx.doi.org/10.1186/1756-0500-3-24 Text en Copyright ©2010 Mallardo et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Report Rossi, Annalisa D'Urso, Oscar F Gatto, Graziana Poltronieri, Palmiro Ferracin, Manuela Remondelli, Paolo Negrini, Massimo Caporaso, Maria G Bonatti, Stefano Mallardo, Massimo Non-coding RNAs change their expression profile after Retinoid induced differentiation of the promyelocytic cell line NB4 |
title | Non-coding RNAs change their expression profile after Retinoid induced differentiation of the promyelocytic cell line NB4 |
title_full | Non-coding RNAs change their expression profile after Retinoid induced differentiation of the promyelocytic cell line NB4 |
title_fullStr | Non-coding RNAs change their expression profile after Retinoid induced differentiation of the promyelocytic cell line NB4 |
title_full_unstemmed | Non-coding RNAs change their expression profile after Retinoid induced differentiation of the promyelocytic cell line NB4 |
title_short | Non-coding RNAs change their expression profile after Retinoid induced differentiation of the promyelocytic cell line NB4 |
title_sort | non-coding rnas change their expression profile after retinoid induced differentiation of the promyelocytic cell line nb4 |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2843733/ https://www.ncbi.nlm.nih.gov/pubmed/20181027 http://dx.doi.org/10.1186/1756-0500-3-24 |
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