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Polymorphisms within inflammatory genes and colorectal cancer
BACKGROUND: Chronic inflammation is a risk factor for colorectal cancer and polymorphisms in the inflammatory genes could modulate the levels of inflammation. We have investigated ten single nucleotide polymorphisms (SNPs) in the following inflammation-related genes: TLR4 (Asp299Gly), CD14 (-260 T&g...
Autores principales: | , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1634873/ https://www.ncbi.nlm.nih.gov/pubmed/17062130 http://dx.doi.org/10.1186/1477-5751-5-15 |
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author | Landi, Stefano Gemignani, Federica Bottari, Fabio Gioia-Patricola, Lydie Guino, Elisabet Cambray, María Biondo, Sebastiano Capella, Gabriel Boldrini, Laura Canzian, Federico Moreno, Victor |
author_facet | Landi, Stefano Gemignani, Federica Bottari, Fabio Gioia-Patricola, Lydie Guino, Elisabet Cambray, María Biondo, Sebastiano Capella, Gabriel Boldrini, Laura Canzian, Federico Moreno, Victor |
author_sort | Landi, Stefano |
collection | PubMed |
description | BACKGROUND: Chronic inflammation is a risk factor for colorectal cancer and polymorphisms in the inflammatory genes could modulate the levels of inflammation. We have investigated ten single nucleotide polymorphisms (SNPs) in the following inflammation-related genes: TLR4 (Asp299Gly), CD14 (-260 T>C), MCP1 (-2518 A>G), IL12A (+7506 A>T, +8707 A>G, +9177 T>A, +9508 G>A), NOS2A (+524T>C), TNF (-857C>T), and PTGS1 (V444I) in 377 colorectal (CRC) cancer cases and 326 controls from Barcelona (Spain). RESULTS: There was no statistically significant association between the SNPs investigated and colorectal cancer risk. CONCLUSION: The lack of association may show that the inflammatory genes selected for this study are not involved in the carcinogenic process of colorectum. Alternatively, the negative results may derive from no particular biological effect of the analysed polymorphisms in relation to CRC. Otherwise, the eventual biological effect is so little to go undetected, unless analysing a much larger sample size. |
format | Text |
id | pubmed-1634873 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-16348732006-11-07 Polymorphisms within inflammatory genes and colorectal cancer Landi, Stefano Gemignani, Federica Bottari, Fabio Gioia-Patricola, Lydie Guino, Elisabet Cambray, María Biondo, Sebastiano Capella, Gabriel Boldrini, Laura Canzian, Federico Moreno, Victor J Negat Results Biomed Research BACKGROUND: Chronic inflammation is a risk factor for colorectal cancer and polymorphisms in the inflammatory genes could modulate the levels of inflammation. We have investigated ten single nucleotide polymorphisms (SNPs) in the following inflammation-related genes: TLR4 (Asp299Gly), CD14 (-260 T>C), MCP1 (-2518 A>G), IL12A (+7506 A>T, +8707 A>G, +9177 T>A, +9508 G>A), NOS2A (+524T>C), TNF (-857C>T), and PTGS1 (V444I) in 377 colorectal (CRC) cancer cases and 326 controls from Barcelona (Spain). RESULTS: There was no statistically significant association between the SNPs investigated and colorectal cancer risk. CONCLUSION: The lack of association may show that the inflammatory genes selected for this study are not involved in the carcinogenic process of colorectum. Alternatively, the negative results may derive from no particular biological effect of the analysed polymorphisms in relation to CRC. Otherwise, the eventual biological effect is so little to go undetected, unless analysing a much larger sample size. BioMed Central 2006-10-24 /pmc/articles/PMC1634873/ /pubmed/17062130 http://dx.doi.org/10.1186/1477-5751-5-15 Text en Copyright © 2006 Landi 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. |
spellingShingle | Research Landi, Stefano Gemignani, Federica Bottari, Fabio Gioia-Patricola, Lydie Guino, Elisabet Cambray, María Biondo, Sebastiano Capella, Gabriel Boldrini, Laura Canzian, Federico Moreno, Victor Polymorphisms within inflammatory genes and colorectal cancer |
title | Polymorphisms within inflammatory genes and colorectal cancer |
title_full | Polymorphisms within inflammatory genes and colorectal cancer |
title_fullStr | Polymorphisms within inflammatory genes and colorectal cancer |
title_full_unstemmed | Polymorphisms within inflammatory genes and colorectal cancer |
title_short | Polymorphisms within inflammatory genes and colorectal cancer |
title_sort | polymorphisms within inflammatory genes and colorectal cancer |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1634873/ https://www.ncbi.nlm.nih.gov/pubmed/17062130 http://dx.doi.org/10.1186/1477-5751-5-15 |
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