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A Quest for miRNA Bio-Marker: A Track Back Approach from Gingivo Buccal Cancer to Two Different Types of Precancers

Deregulation of miRNA expression may contribute to tumorigenesis and other patho-physiology associated with cancer. Using TLDA, expression of 762 miRNAs was checked in 18 pairs of gingivo buccal cancer-adjacent control tissues. Expression of significantly deregulated miRNAs was further validated in...

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Autores principales: De Sarkar, Navonil, Roy, Roshni, Mitra, Jit Kumar, Ghose, Sandip, Chakraborty, Arnab, Paul, Ranjan Rashmi, Mukhopadhyay, Indranil, Roy, Bidyut
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4134240/
https://www.ncbi.nlm.nih.gov/pubmed/25126847
http://dx.doi.org/10.1371/journal.pone.0104839
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author De Sarkar, Navonil
Roy, Roshni
Mitra, Jit Kumar
Ghose, Sandip
Chakraborty, Arnab
Paul, Ranjan Rashmi
Mukhopadhyay, Indranil
Roy, Bidyut
author_facet De Sarkar, Navonil
Roy, Roshni
Mitra, Jit Kumar
Ghose, Sandip
Chakraborty, Arnab
Paul, Ranjan Rashmi
Mukhopadhyay, Indranil
Roy, Bidyut
author_sort De Sarkar, Navonil
collection PubMed
description Deregulation of miRNA expression may contribute to tumorigenesis and other patho-physiology associated with cancer. Using TLDA, expression of 762 miRNAs was checked in 18 pairs of gingivo buccal cancer-adjacent control tissues. Expression of significantly deregulated miRNAs was further validated in cancer and examined in two types of precancer (leukoplakia and lichen planus) tissues by primer-specific TaqMan assays. Biological implications of these miRNAs were assessed bioinformatically. Expression of hsa-miR-1293, hsa-miR-31, hsa-miR-31* and hsa-miR-7 were significantly up-regulated and those of hsa-miR-206, hsa-miR-204 and hsa-miR-133a were significantly down-regulated in all cancer samples. Expression of only hsa-miR-31 was significantly up-regulated in leukoplakia but none in lichen planus samples. Analysis of expression heterogeneity divided 18 cancer samples into clusters of 13 and 5 samples and revealed that expression of 30 miRNAs (including the above-mentioned 7 miRNAs), was significantly deregulated in the cluster of 13 samples. From database mining and pathway analysis it was observed that these miRNAs can significantly target many of the genes present in different cancer related pathways such as “proteoglycans in cancer”, PI3K-AKT etc. which play important roles in expression of different molecular features of cancer. Expression of hsa-miR-31 was significantly up-regulated in both cancer and leukoplakia tissues and, thus, may be one of the molecular markers of leukoplakia which may progress to gingivo-buccal cancer.
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spelling pubmed-41342402014-08-19 A Quest for miRNA Bio-Marker: A Track Back Approach from Gingivo Buccal Cancer to Two Different Types of Precancers De Sarkar, Navonil Roy, Roshni Mitra, Jit Kumar Ghose, Sandip Chakraborty, Arnab Paul, Ranjan Rashmi Mukhopadhyay, Indranil Roy, Bidyut PLoS One Research Article Deregulation of miRNA expression may contribute to tumorigenesis and other patho-physiology associated with cancer. Using TLDA, expression of 762 miRNAs was checked in 18 pairs of gingivo buccal cancer-adjacent control tissues. Expression of significantly deregulated miRNAs was further validated in cancer and examined in two types of precancer (leukoplakia and lichen planus) tissues by primer-specific TaqMan assays. Biological implications of these miRNAs were assessed bioinformatically. Expression of hsa-miR-1293, hsa-miR-31, hsa-miR-31* and hsa-miR-7 were significantly up-regulated and those of hsa-miR-206, hsa-miR-204 and hsa-miR-133a were significantly down-regulated in all cancer samples. Expression of only hsa-miR-31 was significantly up-regulated in leukoplakia but none in lichen planus samples. Analysis of expression heterogeneity divided 18 cancer samples into clusters of 13 and 5 samples and revealed that expression of 30 miRNAs (including the above-mentioned 7 miRNAs), was significantly deregulated in the cluster of 13 samples. From database mining and pathway analysis it was observed that these miRNAs can significantly target many of the genes present in different cancer related pathways such as “proteoglycans in cancer”, PI3K-AKT etc. which play important roles in expression of different molecular features of cancer. Expression of hsa-miR-31 was significantly up-regulated in both cancer and leukoplakia tissues and, thus, may be one of the molecular markers of leukoplakia which may progress to gingivo-buccal cancer. Public Library of Science 2014-08-15 /pmc/articles/PMC4134240/ /pubmed/25126847 http://dx.doi.org/10.1371/journal.pone.0104839 Text en © 2014 De Sarkar et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
De Sarkar, Navonil
Roy, Roshni
Mitra, Jit Kumar
Ghose, Sandip
Chakraborty, Arnab
Paul, Ranjan Rashmi
Mukhopadhyay, Indranil
Roy, Bidyut
A Quest for miRNA Bio-Marker: A Track Back Approach from Gingivo Buccal Cancer to Two Different Types of Precancers
title A Quest for miRNA Bio-Marker: A Track Back Approach from Gingivo Buccal Cancer to Two Different Types of Precancers
title_full A Quest for miRNA Bio-Marker: A Track Back Approach from Gingivo Buccal Cancer to Two Different Types of Precancers
title_fullStr A Quest for miRNA Bio-Marker: A Track Back Approach from Gingivo Buccal Cancer to Two Different Types of Precancers
title_full_unstemmed A Quest for miRNA Bio-Marker: A Track Back Approach from Gingivo Buccal Cancer to Two Different Types of Precancers
title_short A Quest for miRNA Bio-Marker: A Track Back Approach from Gingivo Buccal Cancer to Two Different Types of Precancers
title_sort quest for mirna bio-marker: a track back approach from gingivo buccal cancer to two different types of precancers
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4134240/
https://www.ncbi.nlm.nih.gov/pubmed/25126847
http://dx.doi.org/10.1371/journal.pone.0104839
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