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Associations of ICOS and PD.1 Gene Variants with Colon Cancer Risk in The Iranian Population
BACKGROUND: Positive and negative co-stimulatory molecules are important factors determining the outcome of immune responses to the presence of tumors. Since co-stimulatory molecule expression may be affected by gene polymorphisms, we aimed to investigate associations between variants of PD.1 and IC...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
West Asia Organization for Cancer Prevention
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5980843/ https://www.ncbi.nlm.nih.gov/pubmed/29580042 http://dx.doi.org/10.22034/APJCP.2018.19.3.693 |
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author | Shamsdin, Seyedeh Azra Karimi, Mohammad Hossein Hosseini, Seyed Vahid Geramizadeh, Bita Fattahi, Mohamad Reza Mehrabani, Davood Moravej, Ali |
author_facet | Shamsdin, Seyedeh Azra Karimi, Mohammad Hossein Hosseini, Seyed Vahid Geramizadeh, Bita Fattahi, Mohamad Reza Mehrabani, Davood Moravej, Ali |
author_sort | Shamsdin, Seyedeh Azra |
collection | PubMed |
description | BACKGROUND: Positive and negative co-stimulatory molecules are important factors determining the outcome of immune responses to the presence of tumors. Since co-stimulatory molecule expression may be affected by gene polymorphisms, we aimed to investigate associations between variants of PD.1 and ICOS and susceptibility to colon cancer. MATERIAL AND METHODS: ICOS (-693A/G), ICOS (+1720C/T) and PD.1 (-538G/A) gene polymorphisms were evaluated by the PCR-RFLP method in 76 colon cancer patients and 73 healthy controls. RESULTS: The frequencies of the GG genotype and the G allele at position -693 of the ICOS gene were significantly higher in the patient group (P=0.014 and p=0.0002), while the AA genotype was significantly more common in controls (P=0.0016). At position -538 of PD.1, GG genotype and G allele frequencies were higher in the patient group (P<0.0001and P<0.0001). Again, AA and also AG genotypes significantly predominated in controls (P<0.0001 and P=0.012). Regarding genotypes and alleles of ICOS at position +1720. Frequencies of GCG and GTG haplotypes were higher in patients compared to those of controls (P=0.016 and P<0.0001), while, frequencies of GTA, ATA and ATG haplotypes were higher in controls (P=0.0017, P<0.0001 and P=0.015). GTG/GTG and GTG/GCG double haplotypes were more frequent in patients compared to controls (P=0.0147 and P=0.0071). CONCLUSION: Our study clarified that PD.1 (-538G/A) and ICOS (-693A/G) gene polymorphisms can be considered as genetic risk factors for the development of colon cancer among Iranian patients. |
format | Online Article Text |
id | pubmed-5980843 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | West Asia Organization for Cancer Prevention |
record_format | MEDLINE/PubMed |
spelling | pubmed-59808432018-06-06 Associations of ICOS and PD.1 Gene Variants with Colon Cancer Risk in The Iranian Population Shamsdin, Seyedeh Azra Karimi, Mohammad Hossein Hosseini, Seyed Vahid Geramizadeh, Bita Fattahi, Mohamad Reza Mehrabani, Davood Moravej, Ali Asian Pac J Cancer Prev Research Article BACKGROUND: Positive and negative co-stimulatory molecules are important factors determining the outcome of immune responses to the presence of tumors. Since co-stimulatory molecule expression may be affected by gene polymorphisms, we aimed to investigate associations between variants of PD.1 and ICOS and susceptibility to colon cancer. MATERIAL AND METHODS: ICOS (-693A/G), ICOS (+1720C/T) and PD.1 (-538G/A) gene polymorphisms were evaluated by the PCR-RFLP method in 76 colon cancer patients and 73 healthy controls. RESULTS: The frequencies of the GG genotype and the G allele at position -693 of the ICOS gene were significantly higher in the patient group (P=0.014 and p=0.0002), while the AA genotype was significantly more common in controls (P=0.0016). At position -538 of PD.1, GG genotype and G allele frequencies were higher in the patient group (P<0.0001and P<0.0001). Again, AA and also AG genotypes significantly predominated in controls (P<0.0001 and P=0.012). Regarding genotypes and alleles of ICOS at position +1720. Frequencies of GCG and GTG haplotypes were higher in patients compared to those of controls (P=0.016 and P<0.0001), while, frequencies of GTA, ATA and ATG haplotypes were higher in controls (P=0.0017, P<0.0001 and P=0.015). GTG/GTG and GTG/GCG double haplotypes were more frequent in patients compared to controls (P=0.0147 and P=0.0071). CONCLUSION: Our study clarified that PD.1 (-538G/A) and ICOS (-693A/G) gene polymorphisms can be considered as genetic risk factors for the development of colon cancer among Iranian patients. West Asia Organization for Cancer Prevention 2018 /pmc/articles/PMC5980843/ /pubmed/29580042 http://dx.doi.org/10.22034/APJCP.2018.19.3.693 Text en Copyright: © Asian Pacific Journal of Cancer Prevention http://creativecommons.org/licenses/BY-SA/4.0 This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License |
spellingShingle | Research Article Shamsdin, Seyedeh Azra Karimi, Mohammad Hossein Hosseini, Seyed Vahid Geramizadeh, Bita Fattahi, Mohamad Reza Mehrabani, Davood Moravej, Ali Associations of ICOS and PD.1 Gene Variants with Colon Cancer Risk in The Iranian Population |
title | Associations of ICOS and PD.1 Gene Variants with Colon Cancer Risk in The Iranian Population |
title_full | Associations of ICOS and PD.1 Gene Variants with Colon Cancer Risk in The Iranian Population |
title_fullStr | Associations of ICOS and PD.1 Gene Variants with Colon Cancer Risk in The Iranian Population |
title_full_unstemmed | Associations of ICOS and PD.1 Gene Variants with Colon Cancer Risk in The Iranian Population |
title_short | Associations of ICOS and PD.1 Gene Variants with Colon Cancer Risk in The Iranian Population |
title_sort | associations of icos and pd.1 gene variants with colon cancer risk in the iranian population |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5980843/ https://www.ncbi.nlm.nih.gov/pubmed/29580042 http://dx.doi.org/10.22034/APJCP.2018.19.3.693 |
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