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1.
Iranian Journal of Public Health. 2014; 43 (4): 453-459
in English | IMEMR | ID: emr-159598

ABSTRACT

The TP53 gene is one of the most frequently mutated genes amongst human malignancies, particularly TP53 codon 72 polymorphism. Furthermore, an association between the TP53 codon 72 variants and prostate cancer has been reported in several studies. Although some studies have indicated an association between the TP53 Arg/Arg variant and an increased risk for prostate cancer, other studies have shown a positive correlation between the TP53 Pro/Pro genotype instead. Therefore, to clarify if this polymorphism is associated with an increased risk of prostate cancer in Iranian men, we conducted a case-control study of 40 sporadic prostate cancer patients and 80 benign prostate hyperplasia cases. The TP53 codon 72 was genotyped using an allele specific PCR. A significant association between the TP53 codon 72 genotype and prostate cancer risk was found [OR = 6.8, 95% CI = [1.8-25.1], P = 0.005]. However, the results of this study did not support an association between age, the Gleason score nor TP53 genotype at codon 72 in prostate cancer patients. TP53 codon 72 polymorphism may have a great impact in the development of prostate cancer

2.
Iranian Journal of Pediatrics. 2011; 21 (1): 58-64
in English | IMEMR | ID: emr-109557

ABSTRACT

Acute respiratory infection [ARI] is the major cause of morbidity and mortality in children worldwide. Human respiratory syncytial virus [HRSV] is main viral agent of ARI in infants and young children in terms of effect and prevalence. The aim of this study was to investigate HRSV genotypes during one season in Iran. In this cross-sectional study, 107 throat swabs were collected from children less than 5 years of age with acute respiratory infection from October to December 2009. The respiratory samples were obtained from several provinces: Tehran, Isfahan, Hamadan, Zanjan, Kordestan, Lorestan and West Azarbayjan, and were tested for G protein gene of HRSV by RT-PCR. Of the 107 respiratory samples, 24 [22.42%] were positive for HRSV, of which 16 [66.6%] belonged to subgroup A and 8 [33.4%] to subgroup B. Phylogenetic analysis revealed that subgroup A strains fell in two genotypes GA1 and GA2, whereas subgroup B strains clustered in genotype BA. This study revealed that multiple genotypes of HRSV cocirculated during the season 2009 in Iran. Also subgroup A strains were more prevalent than subgroup B strains, and genotype GA1 was predominant during the season


Subject(s)
Humans , Genetic Variation , GTP-Binding Proteins/genetics , Child , Genotype , Seasons , Respiratory Tract Infections , Acute Disease , Cross-Sectional Studies
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