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Genome expression analysis by suppression subtractive hybridization identified overexpression of Humanin, a target gene in gastric cancer chemoresistance

BACKGROUND: In cancer cells, apoptosis is an important mechanism that influences the outcome of chemotherapy and the development of chemoresistance. To find the genes involved in chemoresistance and the development of gastric cancer, we used the suppression subtractive hybridization method to identi...

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Autores principales: Mottaghi-Dastjerdi, Negar, Soltany-Rezaee-Rad, Mohammad, Sepehrizadeh, Zargham, Roshandel, Gholamreza, Ebrahimifard, Farzaneh, Setayesh, Neda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3896685/
https://www.ncbi.nlm.nih.gov/pubmed/24401285
http://dx.doi.org/10.1186/2008-2231-22-14
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author Mottaghi-Dastjerdi, Negar
Soltany-Rezaee-Rad, Mohammad
Sepehrizadeh, Zargham
Roshandel, Gholamreza
Ebrahimifard, Farzaneh
Setayesh, Neda
author_facet Mottaghi-Dastjerdi, Negar
Soltany-Rezaee-Rad, Mohammad
Sepehrizadeh, Zargham
Roshandel, Gholamreza
Ebrahimifard, Farzaneh
Setayesh, Neda
author_sort Mottaghi-Dastjerdi, Negar
collection PubMed
description BACKGROUND: In cancer cells, apoptosis is an important mechanism that influences the outcome of chemotherapy and the development of chemoresistance. To find the genes involved in chemoresistance and the development of gastric cancer, we used the suppression subtractive hybridization method to identify the genes that are overexpressed in gastric cancer tissues compared to normal gastric tissues. RESULTS: In the suppression subtractive hybridization library we constructed, the most highly overexpressed genes were humanin isoforms. Humanin is a recently identified endogenous peptide that has anti-apoptotic activity and has been selected for further study due to its potential role in the chemoresistance of gastric cancer. Upregulation of humanin isoforms was also observed in clinical samples by using quantitative real-time PCR. Among the studied isoforms, humanin isoform 3, with an expression level of 4.166 ± 1.44 fold, was the most overexpressed isoform in GC. CONCLUSIONS: The overexpression of humanin in gastric cancer suggests a role for chemoresistance and provides new insight into the biology of gastric cancer. We propose that humanin isoforms are novel targets for combating chemoresistance in gastric cancer.
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spelling pubmed-38966852014-01-31 Genome expression analysis by suppression subtractive hybridization identified overexpression of Humanin, a target gene in gastric cancer chemoresistance Mottaghi-Dastjerdi, Negar Soltany-Rezaee-Rad, Mohammad Sepehrizadeh, Zargham Roshandel, Gholamreza Ebrahimifard, Farzaneh Setayesh, Neda Daru Research Article BACKGROUND: In cancer cells, apoptosis is an important mechanism that influences the outcome of chemotherapy and the development of chemoresistance. To find the genes involved in chemoresistance and the development of gastric cancer, we used the suppression subtractive hybridization method to identify the genes that are overexpressed in gastric cancer tissues compared to normal gastric tissues. RESULTS: In the suppression subtractive hybridization library we constructed, the most highly overexpressed genes were humanin isoforms. Humanin is a recently identified endogenous peptide that has anti-apoptotic activity and has been selected for further study due to its potential role in the chemoresistance of gastric cancer. Upregulation of humanin isoforms was also observed in clinical samples by using quantitative real-time PCR. Among the studied isoforms, humanin isoform 3, with an expression level of 4.166 ± 1.44 fold, was the most overexpressed isoform in GC. CONCLUSIONS: The overexpression of humanin in gastric cancer suggests a role for chemoresistance and provides new insight into the biology of gastric cancer. We propose that humanin isoforms are novel targets for combating chemoresistance in gastric cancer. BioMed Central 2014-01-08 /pmc/articles/PMC3896685/ /pubmed/24401285 http://dx.doi.org/10.1186/2008-2231-22-14 Text en Copyright © 2014 Mottaghi-Dastjerdi 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. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Mottaghi-Dastjerdi, Negar
Soltany-Rezaee-Rad, Mohammad
Sepehrizadeh, Zargham
Roshandel, Gholamreza
Ebrahimifard, Farzaneh
Setayesh, Neda
Genome expression analysis by suppression subtractive hybridization identified overexpression of Humanin, a target gene in gastric cancer chemoresistance
title Genome expression analysis by suppression subtractive hybridization identified overexpression of Humanin, a target gene in gastric cancer chemoresistance
title_full Genome expression analysis by suppression subtractive hybridization identified overexpression of Humanin, a target gene in gastric cancer chemoresistance
title_fullStr Genome expression analysis by suppression subtractive hybridization identified overexpression of Humanin, a target gene in gastric cancer chemoresistance
title_full_unstemmed Genome expression analysis by suppression subtractive hybridization identified overexpression of Humanin, a target gene in gastric cancer chemoresistance
title_short Genome expression analysis by suppression subtractive hybridization identified overexpression of Humanin, a target gene in gastric cancer chemoresistance
title_sort genome expression analysis by suppression subtractive hybridization identified overexpression of humanin, a target gene in gastric cancer chemoresistance
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3896685/
https://www.ncbi.nlm.nih.gov/pubmed/24401285
http://dx.doi.org/10.1186/2008-2231-22-14
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