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Correlation study of GAPDH, Bcl-2, and Bax protein immunoexpression in patients with colorectal adenocarcinoma

INTRODUCTION: Colorectal cancer (CRC) is the third and second most commonly diagnosed cancer worldwide in males and females, respectively. Despite prominent progress in diagnosis and treatment, the recurrence rates are still high. A tumour hypoxic environment leads to an increase in glycolytic metab...

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Autores principales: Brzozowa-Zasada, Marlena, Kurek, Józef, Piecuch, Adam, Stęplewska, Katarzyna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6300847/
https://www.ncbi.nlm.nih.gov/pubmed/30581507
http://dx.doi.org/10.5114/pg.2018.79813
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author Brzozowa-Zasada, Marlena
Kurek, Józef
Piecuch, Adam
Stęplewska, Katarzyna
author_facet Brzozowa-Zasada, Marlena
Kurek, Józef
Piecuch, Adam
Stęplewska, Katarzyna
author_sort Brzozowa-Zasada, Marlena
collection PubMed
description INTRODUCTION: Colorectal cancer (CRC) is the third and second most commonly diagnosed cancer worldwide in males and females, respectively. Despite prominent progress in diagnosis and treatment, the recurrence rates are still high. A tumour hypoxic environment leads to an increase in glycolytic metabolism. The crucial intermediate component of glycolysis, glyceraldehyde-3-phosphate dehydrogenase (GAPDH), could play a significant role in cancer progression. An increased level of GAPDH has been described in oncogene-induced transformation and anti-apoptotic function. In other studies, GAPDH has been involved in apoptosis induction. AIM: We examined colorectal adenocarcinoma samples to assess the immunoexpression of GAPDH protein. We also evaluated the correlation between the expression of GAPDH protein and apoptotic parameters including expression of Bcl2 and Bax. MATERIAL AND METHODS: Paraffin sections were incubated for 60 min with primary antibody against GAPDH, Bcl-2, and Bax. RESULTS: Results of our study have shown that GAPDH expression in colorectal cancer is upregulated. We revealed significant positive correlation between expression of this protein and grade and size of tumour, and regional lymph node involvement. In the case of apoptosis-associated proteins, e.g. Bcl-2 and Bax, we found negative correlations between expression of these proteins and grade and size of tumour, lymphovascular invasion, and regional lymph node involvement. Finally, we demonstrated that GAPDH up-regulation is connected with down-regulation in Bcl-2 and Bax. CONCLUSIONS: Up-regulation of GAPDH protein and down-regulation of Bcl-2 and Bax may result in increased of cancer.
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spelling pubmed-63008472018-12-21 Correlation study of GAPDH, Bcl-2, and Bax protein immunoexpression in patients with colorectal adenocarcinoma Brzozowa-Zasada, Marlena Kurek, Józef Piecuch, Adam Stęplewska, Katarzyna Prz Gastroenterol Original Paper INTRODUCTION: Colorectal cancer (CRC) is the third and second most commonly diagnosed cancer worldwide in males and females, respectively. Despite prominent progress in diagnosis and treatment, the recurrence rates are still high. A tumour hypoxic environment leads to an increase in glycolytic metabolism. The crucial intermediate component of glycolysis, glyceraldehyde-3-phosphate dehydrogenase (GAPDH), could play a significant role in cancer progression. An increased level of GAPDH has been described in oncogene-induced transformation and anti-apoptotic function. In other studies, GAPDH has been involved in apoptosis induction. AIM: We examined colorectal adenocarcinoma samples to assess the immunoexpression of GAPDH protein. We also evaluated the correlation between the expression of GAPDH protein and apoptotic parameters including expression of Bcl2 and Bax. MATERIAL AND METHODS: Paraffin sections were incubated for 60 min with primary antibody against GAPDH, Bcl-2, and Bax. RESULTS: Results of our study have shown that GAPDH expression in colorectal cancer is upregulated. We revealed significant positive correlation between expression of this protein and grade and size of tumour, and regional lymph node involvement. In the case of apoptosis-associated proteins, e.g. Bcl-2 and Bax, we found negative correlations between expression of these proteins and grade and size of tumour, lymphovascular invasion, and regional lymph node involvement. Finally, we demonstrated that GAPDH up-regulation is connected with down-regulation in Bcl-2 and Bax. CONCLUSIONS: Up-regulation of GAPDH protein and down-regulation of Bcl-2 and Bax may result in increased of cancer. Termedia Publishing House 2018-12-11 2018 /pmc/articles/PMC6300847/ /pubmed/30581507 http://dx.doi.org/10.5114/pg.2018.79813 Text en Copyright: © 2018 Termedia Sp. z o. o. http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Original Paper
Brzozowa-Zasada, Marlena
Kurek, Józef
Piecuch, Adam
Stęplewska, Katarzyna
Correlation study of GAPDH, Bcl-2, and Bax protein immunoexpression in patients with colorectal adenocarcinoma
title Correlation study of GAPDH, Bcl-2, and Bax protein immunoexpression in patients with colorectal adenocarcinoma
title_full Correlation study of GAPDH, Bcl-2, and Bax protein immunoexpression in patients with colorectal adenocarcinoma
title_fullStr Correlation study of GAPDH, Bcl-2, and Bax protein immunoexpression in patients with colorectal adenocarcinoma
title_full_unstemmed Correlation study of GAPDH, Bcl-2, and Bax protein immunoexpression in patients with colorectal adenocarcinoma
title_short Correlation study of GAPDH, Bcl-2, and Bax protein immunoexpression in patients with colorectal adenocarcinoma
title_sort correlation study of gapdh, bcl-2, and bax protein immunoexpression in patients with colorectal adenocarcinoma
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6300847/
https://www.ncbi.nlm.nih.gov/pubmed/30581507
http://dx.doi.org/10.5114/pg.2018.79813
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