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Interleukin-10 (1082G/A) Polymorphism is Associated with Susceptibility of Acute Myeloid Leukemia Patients in Sudanese Population

BACKGROUND: Interleukin-10 (IL-10) is a multifunctional cytokine with both immunosuppressive and anti-angiogenicfunctions and may have both tumor-promoting and -inhibiting properties. We examined the association between a single nucleotide polymorphism (SNP) in IL-10 -1082G/A (rs1800896) in Sudanese...

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Autores principales: Mohamed Sharif, Omnia, Hassan, Rosline, Mohammed Basbaeen, Ameen Abdulaziz, Hussien Mohmed, Ayman, Khider Ibrahim, Ibrahim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: West Asia Organization for Cancer Prevention 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6745212/
https://www.ncbi.nlm.nih.gov/pubmed/31350948
http://dx.doi.org/10.31557/APJCP.2019.20.7.1939
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author Mohamed Sharif, Omnia
Hassan, Rosline
Mohammed Basbaeen, Ameen Abdulaziz
Hussien Mohmed, Ayman
Khider Ibrahim, Ibrahim
author_facet Mohamed Sharif, Omnia
Hassan, Rosline
Mohammed Basbaeen, Ameen Abdulaziz
Hussien Mohmed, Ayman
Khider Ibrahim, Ibrahim
author_sort Mohamed Sharif, Omnia
collection PubMed
description BACKGROUND: Interleukin-10 (IL-10) is a multifunctional cytokine with both immunosuppressive and anti-angiogenicfunctions and may have both tumor-promoting and -inhibiting properties. We examined the association between a single nucleotide polymorphism (SNP) in IL-10 -1082G/A (rs1800896) in Sudanese acute myeloid leukemia (AML) patients and to assess the association between polymorphisms in IL-10 -1082G/A (rs1800896) and the hematological profile in Sudanese patients with AML. METHODS: A total of 30 patients with acute myeloid leukemia and 30 control subjects were enrolled in this study. Blood samples were collected from all patients in EDTA containing tubes. Genomic DNA was extracted from all blood samples using salting out method. The genotypic variants of IL-10 (-1082G/A) polymorphism were detected by allele specific-PCR. RESULTS: We found that (36.7%) of patients have homogenous GG genotype, (43.3%) have heterogeneous GA genotype and (20.0%) have AA genotype. GA genotype was significantly associated with higher risk of AML compared with the homozygous Genotypes (GG and AA), there is no association between IL-10 (-1082G/A) polymorphism and AML sub-type, gender, age group, mean of hematological parameters. CONCLUSION: Our study concluded that GA genotype of IL-10 -1082G/A (rs1800896) polymorphism is a risk factor for AML and G allele is insignificantly higher than A allele in AML patient. No association between IL-10 (-1082G/A) polymorphism and AML sub-type, gender, age group, mean of hematological parameters.
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spelling pubmed-67452122019-10-03 Interleukin-10 (1082G/A) Polymorphism is Associated with Susceptibility of Acute Myeloid Leukemia Patients in Sudanese Population Mohamed Sharif, Omnia Hassan, Rosline Mohammed Basbaeen, Ameen Abdulaziz Hussien Mohmed, Ayman Khider Ibrahim, Ibrahim Asian Pac J Cancer Prev Short Communication BACKGROUND: Interleukin-10 (IL-10) is a multifunctional cytokine with both immunosuppressive and anti-angiogenicfunctions and may have both tumor-promoting and -inhibiting properties. We examined the association between a single nucleotide polymorphism (SNP) in IL-10 -1082G/A (rs1800896) in Sudanese acute myeloid leukemia (AML) patients and to assess the association between polymorphisms in IL-10 -1082G/A (rs1800896) and the hematological profile in Sudanese patients with AML. METHODS: A total of 30 patients with acute myeloid leukemia and 30 control subjects were enrolled in this study. Blood samples were collected from all patients in EDTA containing tubes. Genomic DNA was extracted from all blood samples using salting out method. The genotypic variants of IL-10 (-1082G/A) polymorphism were detected by allele specific-PCR. RESULTS: We found that (36.7%) of patients have homogenous GG genotype, (43.3%) have heterogeneous GA genotype and (20.0%) have AA genotype. GA genotype was significantly associated with higher risk of AML compared with the homozygous Genotypes (GG and AA), there is no association between IL-10 (-1082G/A) polymorphism and AML sub-type, gender, age group, mean of hematological parameters. CONCLUSION: Our study concluded that GA genotype of IL-10 -1082G/A (rs1800896) polymorphism is a risk factor for AML and G allele is insignificantly higher than A allele in AML patient. No association between IL-10 (-1082G/A) polymorphism and AML sub-type, gender, age group, mean of hematological parameters. West Asia Organization for Cancer Prevention 2019 /pmc/articles/PMC6745212/ /pubmed/31350948 http://dx.doi.org/10.31557/APJCP.2019.20.7.1939 Text en © Asian Pacific Journal of Cancer Prevention This work is licensed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License (https://creativecommons.org/licenses/by-nc-sa/4.0/)
spellingShingle Short Communication
Mohamed Sharif, Omnia
Hassan, Rosline
Mohammed Basbaeen, Ameen Abdulaziz
Hussien Mohmed, Ayman
Khider Ibrahim, Ibrahim
Interleukin-10 (1082G/A) Polymorphism is Associated with Susceptibility of Acute Myeloid Leukemia Patients in Sudanese Population
title Interleukin-10 (1082G/A) Polymorphism is Associated with Susceptibility of Acute Myeloid Leukemia Patients in Sudanese Population
title_full Interleukin-10 (1082G/A) Polymorphism is Associated with Susceptibility of Acute Myeloid Leukemia Patients in Sudanese Population
title_fullStr Interleukin-10 (1082G/A) Polymorphism is Associated with Susceptibility of Acute Myeloid Leukemia Patients in Sudanese Population
title_full_unstemmed Interleukin-10 (1082G/A) Polymorphism is Associated with Susceptibility of Acute Myeloid Leukemia Patients in Sudanese Population
title_short Interleukin-10 (1082G/A) Polymorphism is Associated with Susceptibility of Acute Myeloid Leukemia Patients in Sudanese Population
title_sort interleukin-10 (1082g/a) polymorphism is associated with susceptibility of acute myeloid leukemia patients in sudanese population
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6745212/
https://www.ncbi.nlm.nih.gov/pubmed/31350948
http://dx.doi.org/10.31557/APJCP.2019.20.7.1939
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