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The importance of G2677T/A and C3435T polymorphisms of the MDR1 gene in the aetiology of colorectal cancer

INTRODUCTION: Colorectal cancer (CRC) is the most common cancer among patients, and its aetiology is still not precisely known. It is believed that 15–30% of colorectal cancers are genetically determined. P-glycoprotein (P-gp) encoded by the MDR1 gene in normal conditions plays an important role in...

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Autores principales: Stańko, Grzegorz, Kamiński, Marek, Bogacz, Anna, Seremak-Mrozikiewicz, Agnieszka, Kosiński, Bogusław, Bartkowiak-Wieczorek, Joanna, Kotrych, Daniel, Czerny, Bogusław
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4814531/
https://www.ncbi.nlm.nih.gov/pubmed/27110309
http://dx.doi.org/10.5114/pg.2015.51185
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author Stańko, Grzegorz
Kamiński, Marek
Bogacz, Anna
Seremak-Mrozikiewicz, Agnieszka
Kosiński, Bogusław
Bartkowiak-Wieczorek, Joanna
Kotrych, Daniel
Czerny, Bogusław
author_facet Stańko, Grzegorz
Kamiński, Marek
Bogacz, Anna
Seremak-Mrozikiewicz, Agnieszka
Kosiński, Bogusław
Bartkowiak-Wieczorek, Joanna
Kotrych, Daniel
Czerny, Bogusław
author_sort Stańko, Grzegorz
collection PubMed
description INTRODUCTION: Colorectal cancer (CRC) is the most common cancer among patients, and its aetiology is still not precisely known. It is believed that 15–30% of colorectal cancers are genetically determined. P-glycoprotein (P-gp) encoded by the MDR1 gene in normal conditions plays an important role in the action of colon epithelial cells. However, the MDR1 polymorphism influences the P-gp expression and can weaken its effect against xenobiotics (procarcinogens) and increase the frequency of CRC. AIM: To evaluate the correlation between the MDR1 C3435T and G2677T/A polymorphisms and the risk of colorectal cancer. MATERIAL AND METHODS: The study group with colorectal cancer included 47 women and 60 men while the control group consisted of 110 healthy patients. The diagnosis in patients suffering from CRC was confirmed by histopathological report. Genetic analysis was performed using PCR-RFLP method. RESULTS: We showed only a correlation between the frequency of CT and TT genotypes of C3435T polymorphism and the risk of colorectal cancer in younger age. There was no correlation between the C3435T and G2677T/A polymorphisms of the MDR1 gene and other clinical parameters. CONCLUSIONS: Our findings suggest that T allele carriers of C3435T polymorphism have an increased risk of CRC. However, further studies are needed on a much larger number of patients and genes associated with metabolism and transport of xenobiotics including procarcinogens.
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spelling pubmed-48145312016-04-22 The importance of G2677T/A and C3435T polymorphisms of the MDR1 gene in the aetiology of colorectal cancer Stańko, Grzegorz Kamiński, Marek Bogacz, Anna Seremak-Mrozikiewicz, Agnieszka Kosiński, Bogusław Bartkowiak-Wieczorek, Joanna Kotrych, Daniel Czerny, Bogusław Prz Gastroenterol Original Paper INTRODUCTION: Colorectal cancer (CRC) is the most common cancer among patients, and its aetiology is still not precisely known. It is believed that 15–30% of colorectal cancers are genetically determined. P-glycoprotein (P-gp) encoded by the MDR1 gene in normal conditions plays an important role in the action of colon epithelial cells. However, the MDR1 polymorphism influences the P-gp expression and can weaken its effect against xenobiotics (procarcinogens) and increase the frequency of CRC. AIM: To evaluate the correlation between the MDR1 C3435T and G2677T/A polymorphisms and the risk of colorectal cancer. MATERIAL AND METHODS: The study group with colorectal cancer included 47 women and 60 men while the control group consisted of 110 healthy patients. The diagnosis in patients suffering from CRC was confirmed by histopathological report. Genetic analysis was performed using PCR-RFLP method. RESULTS: We showed only a correlation between the frequency of CT and TT genotypes of C3435T polymorphism and the risk of colorectal cancer in younger age. There was no correlation between the C3435T and G2677T/A polymorphisms of the MDR1 gene and other clinical parameters. CONCLUSIONS: Our findings suggest that T allele carriers of C3435T polymorphism have an increased risk of CRC. However, further studies are needed on a much larger number of patients and genes associated with metabolism and transport of xenobiotics including procarcinogens. Termedia Publishing House 2015-04-28 2016 /pmc/articles/PMC4814531/ /pubmed/27110309 http://dx.doi.org/10.5114/pg.2015.51185 Text en Copyright © 2015 Termedia 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
Stańko, Grzegorz
Kamiński, Marek
Bogacz, Anna
Seremak-Mrozikiewicz, Agnieszka
Kosiński, Bogusław
Bartkowiak-Wieczorek, Joanna
Kotrych, Daniel
Czerny, Bogusław
The importance of G2677T/A and C3435T polymorphisms of the MDR1 gene in the aetiology of colorectal cancer
title The importance of G2677T/A and C3435T polymorphisms of the MDR1 gene in the aetiology of colorectal cancer
title_full The importance of G2677T/A and C3435T polymorphisms of the MDR1 gene in the aetiology of colorectal cancer
title_fullStr The importance of G2677T/A and C3435T polymorphisms of the MDR1 gene in the aetiology of colorectal cancer
title_full_unstemmed The importance of G2677T/A and C3435T polymorphisms of the MDR1 gene in the aetiology of colorectal cancer
title_short The importance of G2677T/A and C3435T polymorphisms of the MDR1 gene in the aetiology of colorectal cancer
title_sort importance of g2677t/a and c3435t polymorphisms of the mdr1 gene in the aetiology of colorectal cancer
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4814531/
https://www.ncbi.nlm.nih.gov/pubmed/27110309
http://dx.doi.org/10.5114/pg.2015.51185
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