Association between gene polymorphism rs11614913 in microRNA196a2, with Non-small cell lung cancer risk in the population of southern Iran

Lung cancer is the most common cause of death worldwide and result in 1.4 million deaths per year. Lung cancer is the fifth most common cancer in Iran, with rates of 4.7 to 9.2 per 100 thousand populations. Despite the low incidence, survival is not promising. Identification of biological markers an...

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Main Authors: Parvin Pishva, Mohammad Tahmaseb, Abbass Ghaderi
Format: Article
Language:English
Published: Kharazmi University 2016-06-01
Series:یافته‌های نوین در علوم زیستی
Subjects:
SNP
Online Access:http://nbr.khu.ac.ir/browse.php?a_code=A-10-35-1&slc_lang=en&sid=1
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spelling doaj-e56768c1ba70480f884af029da690fcf2020-11-24T21:35:57ZengKharazmi Universityیافته‌های نوین در علوم زیستی2423-63302476-71152016-06-01311523Association between gene polymorphism rs11614913 in microRNA196a2, with Non-small cell lung cancer risk in the population of southern IranParvin Pishva0Mohammad Tahmaseb1Abbass Ghaderi2 Lung cancer is the most common cause of death worldwide and result in 1.4 million deaths per year. Lung cancer is the fifth most common cancer in Iran, with rates of 4.7 to 9.2 per 100 thousand populations. Despite the low incidence, survival is not promising. Identification of biological markers and their application in diagnosis of cancer could lead to early diagnosis and therefore longer survival rate in patients. In this study, we evaluated the association of SNP rs11614913 in mir-196a2 with risk of non-small cell lung cancer (NSCLC) in population of southern Iran. SNP rs11614913 in miR-196a2 was assayed in 95 lung cancer patients and 100 controls. Polymorphism was determined by RFLP-PCR. The PCR product was digested with TaaI (5’ ACN^GT) which generated two bands (187bp and 196bp) in TT, three bands (187bp, 196bp and 383bp) in TC and one bandn(383bp) in CC individuals. Analysis of electrophoretic pattern of digestion products revealed that the frequencies of C allele for SNP rs11614913 miR-196a2 were 0.695 in patients and 0.76 in controls. As a result, the genotype frequencies of TT, TC and CC were 0.074, 0.463 and 0.463 in patients and 0.06, 0.36 and 0.58 in controls. The statistical analysis indicates the presence of Hardy-Weinberg equilibrium between the two alleles of the gene in the population studied (p>0.05). Based on the results in this study, no significant association between SNP rs11614913 and susceptibility to NSCLC was found. However, male participants who possess TC/TT genotypes showed high risk for NSCLC compared to those possessed CC genotypes (recessive genetic model).http://nbr.khu.ac.ir/browse.php?a_code=A-10-35-1&slc_lang=en&sid=1micro RNAnon-small cell lung cancerSNP
collection DOAJ
language English
format Article
sources DOAJ
author Parvin Pishva
Mohammad Tahmaseb
Abbass Ghaderi
spellingShingle Parvin Pishva
Mohammad Tahmaseb
Abbass Ghaderi
Association between gene polymorphism rs11614913 in microRNA196a2, with Non-small cell lung cancer risk in the population of southern Iran
یافته‌های نوین در علوم زیستی
micro RNA
non-small cell lung cancer
SNP
author_facet Parvin Pishva
Mohammad Tahmaseb
Abbass Ghaderi
author_sort Parvin Pishva
title Association between gene polymorphism rs11614913 in microRNA196a2, with Non-small cell lung cancer risk in the population of southern Iran
title_short Association between gene polymorphism rs11614913 in microRNA196a2, with Non-small cell lung cancer risk in the population of southern Iran
title_full Association between gene polymorphism rs11614913 in microRNA196a2, with Non-small cell lung cancer risk in the population of southern Iran
title_fullStr Association between gene polymorphism rs11614913 in microRNA196a2, with Non-small cell lung cancer risk in the population of southern Iran
title_full_unstemmed Association between gene polymorphism rs11614913 in microRNA196a2, with Non-small cell lung cancer risk in the population of southern Iran
title_sort association between gene polymorphism rs11614913 in microrna196a2, with non-small cell lung cancer risk in the population of southern iran
publisher Kharazmi University
series یافته‌های نوین در علوم زیستی
issn 2423-6330
2476-7115
publishDate 2016-06-01
description Lung cancer is the most common cause of death worldwide and result in 1.4 million deaths per year. Lung cancer is the fifth most common cancer in Iran, with rates of 4.7 to 9.2 per 100 thousand populations. Despite the low incidence, survival is not promising. Identification of biological markers and their application in diagnosis of cancer could lead to early diagnosis and therefore longer survival rate in patients. In this study, we evaluated the association of SNP rs11614913 in mir-196a2 with risk of non-small cell lung cancer (NSCLC) in population of southern Iran. SNP rs11614913 in miR-196a2 was assayed in 95 lung cancer patients and 100 controls. Polymorphism was determined by RFLP-PCR. The PCR product was digested with TaaI (5’ ACN^GT) which generated two bands (187bp and 196bp) in TT, three bands (187bp, 196bp and 383bp) in TC and one bandn(383bp) in CC individuals. Analysis of electrophoretic pattern of digestion products revealed that the frequencies of C allele for SNP rs11614913 miR-196a2 were 0.695 in patients and 0.76 in controls. As a result, the genotype frequencies of TT, TC and CC were 0.074, 0.463 and 0.463 in patients and 0.06, 0.36 and 0.58 in controls. The statistical analysis indicates the presence of Hardy-Weinberg equilibrium between the two alleles of the gene in the population studied (p>0.05). Based on the results in this study, no significant association between SNP rs11614913 and susceptibility to NSCLC was found. However, male participants who possess TC/TT genotypes showed high risk for NSCLC compared to those possessed CC genotypes (recessive genetic model).
topic micro RNA
non-small cell lung cancer
SNP
url http://nbr.khu.ac.ir/browse.php?a_code=A-10-35-1&slc_lang=en&sid=1
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