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Deregulation of ARID1A, CDH1, cMET and PIK3CA and target-related microRNA expression in gastric cancer

Genetic and epigenetic alterations play an important role in gastric cancer (GC) pathogenesis. Aberrations of the phosphatidylinositol-3-kinase signaling pathway are well described. However, emerging genes have been described such as, the chromatin remodeling gene ARID1A. Our aim was to determine th...

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Autores principales: Ibarrola-Villava, Maider, Llorca-Cardeñosa, Marta J., Tarazona, Noelia, Mongort, Cristina, Fleitas, Tania, Perez-Fidalgo, José Alejandro, Roselló, Susana, Navarro, Samuel, Ribas, Gloria, Cervantes, Andrés
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4694964/
https://www.ncbi.nlm.nih.gov/pubmed/26334097
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author Ibarrola-Villava, Maider
Llorca-Cardeñosa, Marta J.
Tarazona, Noelia
Mongort, Cristina
Fleitas, Tania
Perez-Fidalgo, José Alejandro
Roselló, Susana
Navarro, Samuel
Ribas, Gloria
Cervantes, Andrés
author_facet Ibarrola-Villava, Maider
Llorca-Cardeñosa, Marta J.
Tarazona, Noelia
Mongort, Cristina
Fleitas, Tania
Perez-Fidalgo, José Alejandro
Roselló, Susana
Navarro, Samuel
Ribas, Gloria
Cervantes, Andrés
author_sort Ibarrola-Villava, Maider
collection PubMed
description Genetic and epigenetic alterations play an important role in gastric cancer (GC) pathogenesis. Aberrations of the phosphatidylinositol-3-kinase signaling pathway are well described. However, emerging genes have been described such as, the chromatin remodeling gene ARID1A. Our aim was to determine the expression levels of four GC-related genes, ARID1A, CDH1, cMET and PIK3CA, and 14 target-related microRNAs (miRNAs). We compared mRNA and miRNA expression levels among 66 gastric tumor and normal adjacent mucosa samples using quantitative real-time reverse transcription PCR. Moreover, ARID1A, cMET and PIK3CA protein levels were assessed by immunohistochemistry (IHC). Finally, gene and miRNAs associations with clinical characteristics and outcome were also evaluated. An increased cMET and PIK3CA mRNA expression was found in 78.0% (P = 2.20 × 10(−5)) and 73.8% (P = 1.00 × 10(−3)) of the tumors, respectively. Moreover, IHC revealed that cMET and PIK3CA expression was positive in 63.6% and 87.8% of the tumors, respectively. Six miRNAs had significantly different expression between paired-samples, finding five up-regulated [miR-223-3p (P = 1.65 × 10(−6)), miR-19a-3p (P = 1.23 × 10(−4)), miR-128-3p (P = 3.49 × 10(−4)), miR-130b-3p (P = 1.00 × 10(−3)) and miR-34a-5p (P = 4.00 × 10(−3))] and one down-regulated [miR-124-3p (P = 0.03)]. Our data suggest that cMET, PIK3CA and target-related miRNAs play an important role in GC and may serve as potential targets for therapy.
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spelling pubmed-46949642016-01-20 Deregulation of ARID1A, CDH1, cMET and PIK3CA and target-related microRNA expression in gastric cancer Ibarrola-Villava, Maider Llorca-Cardeñosa, Marta J. Tarazona, Noelia Mongort, Cristina Fleitas, Tania Perez-Fidalgo, José Alejandro Roselló, Susana Navarro, Samuel Ribas, Gloria Cervantes, Andrés Oncotarget Research Paper Genetic and epigenetic alterations play an important role in gastric cancer (GC) pathogenesis. Aberrations of the phosphatidylinositol-3-kinase signaling pathway are well described. However, emerging genes have been described such as, the chromatin remodeling gene ARID1A. Our aim was to determine the expression levels of four GC-related genes, ARID1A, CDH1, cMET and PIK3CA, and 14 target-related microRNAs (miRNAs). We compared mRNA and miRNA expression levels among 66 gastric tumor and normal adjacent mucosa samples using quantitative real-time reverse transcription PCR. Moreover, ARID1A, cMET and PIK3CA protein levels were assessed by immunohistochemistry (IHC). Finally, gene and miRNAs associations with clinical characteristics and outcome were also evaluated. An increased cMET and PIK3CA mRNA expression was found in 78.0% (P = 2.20 × 10(−5)) and 73.8% (P = 1.00 × 10(−3)) of the tumors, respectively. Moreover, IHC revealed that cMET and PIK3CA expression was positive in 63.6% and 87.8% of the tumors, respectively. Six miRNAs had significantly different expression between paired-samples, finding five up-regulated [miR-223-3p (P = 1.65 × 10(−6)), miR-19a-3p (P = 1.23 × 10(−4)), miR-128-3p (P = 3.49 × 10(−4)), miR-130b-3p (P = 1.00 × 10(−3)) and miR-34a-5p (P = 4.00 × 10(−3))] and one down-regulated [miR-124-3p (P = 0.03)]. Our data suggest that cMET, PIK3CA and target-related miRNAs play an important role in GC and may serve as potential targets for therapy. Impact Journals LLC 2015-07-27 /pmc/articles/PMC4694964/ /pubmed/26334097 Text en Copyright: © 2015 Ibarrola-Villava et al. http://creativecommons.org/licenses/by/2.5/ 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 credited.
spellingShingle Research Paper
Ibarrola-Villava, Maider
Llorca-Cardeñosa, Marta J.
Tarazona, Noelia
Mongort, Cristina
Fleitas, Tania
Perez-Fidalgo, José Alejandro
Roselló, Susana
Navarro, Samuel
Ribas, Gloria
Cervantes, Andrés
Deregulation of ARID1A, CDH1, cMET and PIK3CA and target-related microRNA expression in gastric cancer
title Deregulation of ARID1A, CDH1, cMET and PIK3CA and target-related microRNA expression in gastric cancer
title_full Deregulation of ARID1A, CDH1, cMET and PIK3CA and target-related microRNA expression in gastric cancer
title_fullStr Deregulation of ARID1A, CDH1, cMET and PIK3CA and target-related microRNA expression in gastric cancer
title_full_unstemmed Deregulation of ARID1A, CDH1, cMET and PIK3CA and target-related microRNA expression in gastric cancer
title_short Deregulation of ARID1A, CDH1, cMET and PIK3CA and target-related microRNA expression in gastric cancer
title_sort deregulation of arid1a, cdh1, cmet and pik3ca and target-related microrna expression in gastric cancer
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4694964/
https://www.ncbi.nlm.nih.gov/pubmed/26334097
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