MicroRNAs 146a and 147b Biomarkers for Colorectal Tumor’s Localization

The recently identified class of microRNAs (miRs) provided a new insight into cancer research, since abnormalities of members of microRNAs family have been found in various types of cancer. However, the relationship between five miRNAs (miR146a, miR155, miR21, miR135a, and miR147b) and colorectal ca...

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Main Authors: Inés Omrane, Nadia Kourda, Nejla Stambouli, Maud Privat, Imen Medimegh, Amira Arfaoui, Nancy Uhrhammer, Karim Bougatef, Olfa Baroudi, Hassen Bouzaienne, Raja Marrakchi, Yves-Jean Bignon, Amel Benammar-Elgaaied
Format: Article
Language:English
Published: Hindawi Limited 2014-01-01
Series:BioMed Research International
Online Access:http://dx.doi.org/10.1155/2014/584852
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spelling doaj-9af73cb2de8e45eba9a57a0856144fa92020-11-24T22:52:05ZengHindawi LimitedBioMed Research International2314-61332314-61412014-01-01201410.1155/2014/584852584852MicroRNAs 146a and 147b Biomarkers for Colorectal Tumor’s LocalizationInés Omrane0Nadia Kourda1Nejla Stambouli2Maud Privat3Imen Medimegh4Amira Arfaoui5Nancy Uhrhammer6Karim Bougatef7Olfa Baroudi8Hassen Bouzaienne9Raja Marrakchi10Yves-Jean Bignon11Amel Benammar-Elgaaied12Laboratory of Human Genetics Immunology and Pathology, Faculty of Sciences, Tunis El Manar University, 2092 Tunis, TunisiaLaboratory of Anatomy and Pathology, Charles Nicolle Hospital of Tunis, TunisiaLaboratory of Human Genetics Immunology and Pathology, Faculty of Sciences, Tunis El Manar University, 2092 Tunis, TunisiaLaboratory of Diagnosis and Molecular Genetics, Centre Jean Perrin, Clermont Ferrand, FranceLaboratory of Human Genetics Immunology and Pathology, Faculty of Sciences, Tunis El Manar University, 2092 Tunis, TunisiaLaboratory of Anatomy and Pathology, Charles Nicolle Hospital of Tunis, TunisiaLaboratory of Diagnosis and Molecular Genetics, Centre Jean Perrin, Clermont Ferrand, FranceLaboratory of Human Genetics Immunology and Pathology, Faculty of Sciences, Tunis El Manar University, 2092 Tunis, TunisiaLaboratory of Human Genetics Immunology and Pathology, Faculty of Sciences, Tunis El Manar University, 2092 Tunis, TunisiaLaboratory of Human Genetics Immunology and Pathology, Faculty of Sciences, Tunis El Manar University, 2092 Tunis, TunisiaLaboratory of Human Genetics Immunology and Pathology, Faculty of Sciences, Tunis El Manar University, 2092 Tunis, TunisiaLaboratory of Diagnosis and Molecular Genetics, Centre Jean Perrin, Clermont Ferrand, FranceLaboratory of Human Genetics Immunology and Pathology, Faculty of Sciences, Tunis El Manar University, 2092 Tunis, TunisiaThe recently identified class of microRNAs (miRs) provided a new insight into cancer research, since abnormalities of members of microRNAs family have been found in various types of cancer. However, the relationship between five miRNAs (miR146a, miR155, miR21, miR135a, and miR147b) and colorectal cancer remains unclear. In the present study, we examined expression of these miRNAs in 25 pair-matched colon cancer tissues and normal colon mucosa. The expression levels of miR146a, miR155, miR21, miR135a, and miR147b were quantified by real-time PCR. We found that miR21, miR146a, and miR135a were all expressed at higher levels in colon tumors. On the other hand, miR146a and miR147b expressions are significantly higher in left colon compared to right colon. These two miRs, especially miR146a, seemed to be markers for the left colon tumors. Moreover, significant proportional and inverse correlations were found between miR expressions in tumor and healthy tissue, and the correlations profiles were different depending on cancer localization. Taken together, these results lead us to suggest the presence of different mechanisms regulating miRs expression and consequently their target genes in left and right colon. So the pathway of colorectal carcinogenesis would be different according to the site of the tumor.http://dx.doi.org/10.1155/2014/584852
collection DOAJ
language English
format Article
sources DOAJ
author Inés Omrane
Nadia Kourda
Nejla Stambouli
Maud Privat
Imen Medimegh
Amira Arfaoui
Nancy Uhrhammer
Karim Bougatef
Olfa Baroudi
Hassen Bouzaienne
Raja Marrakchi
Yves-Jean Bignon
Amel Benammar-Elgaaied
spellingShingle Inés Omrane
Nadia Kourda
Nejla Stambouli
Maud Privat
Imen Medimegh
Amira Arfaoui
Nancy Uhrhammer
Karim Bougatef
Olfa Baroudi
Hassen Bouzaienne
Raja Marrakchi
Yves-Jean Bignon
Amel Benammar-Elgaaied
MicroRNAs 146a and 147b Biomarkers for Colorectal Tumor’s Localization
BioMed Research International
author_facet Inés Omrane
Nadia Kourda
Nejla Stambouli
Maud Privat
Imen Medimegh
Amira Arfaoui
Nancy Uhrhammer
Karim Bougatef
Olfa Baroudi
Hassen Bouzaienne
Raja Marrakchi
Yves-Jean Bignon
Amel Benammar-Elgaaied
author_sort Inés Omrane
title MicroRNAs 146a and 147b Biomarkers for Colorectal Tumor’s Localization
title_short MicroRNAs 146a and 147b Biomarkers for Colorectal Tumor’s Localization
title_full MicroRNAs 146a and 147b Biomarkers for Colorectal Tumor’s Localization
title_fullStr MicroRNAs 146a and 147b Biomarkers for Colorectal Tumor’s Localization
title_full_unstemmed MicroRNAs 146a and 147b Biomarkers for Colorectal Tumor’s Localization
title_sort micrornas 146a and 147b biomarkers for colorectal tumor’s localization
publisher Hindawi Limited
series BioMed Research International
issn 2314-6133
2314-6141
publishDate 2014-01-01
description The recently identified class of microRNAs (miRs) provided a new insight into cancer research, since abnormalities of members of microRNAs family have been found in various types of cancer. However, the relationship between five miRNAs (miR146a, miR155, miR21, miR135a, and miR147b) and colorectal cancer remains unclear. In the present study, we examined expression of these miRNAs in 25 pair-matched colon cancer tissues and normal colon mucosa. The expression levels of miR146a, miR155, miR21, miR135a, and miR147b were quantified by real-time PCR. We found that miR21, miR146a, and miR135a were all expressed at higher levels in colon tumors. On the other hand, miR146a and miR147b expressions are significantly higher in left colon compared to right colon. These two miRs, especially miR146a, seemed to be markers for the left colon tumors. Moreover, significant proportional and inverse correlations were found between miR expressions in tumor and healthy tissue, and the correlations profiles were different depending on cancer localization. Taken together, these results lead us to suggest the presence of different mechanisms regulating miRs expression and consequently their target genes in left and right colon. So the pathway of colorectal carcinogenesis would be different according to the site of the tumor.
url http://dx.doi.org/10.1155/2014/584852
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