2014
DOI: 10.7314/apjcp.2014.15.6.2631
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Lack of Association of Intron 3 16 bp Polymorphism of TP53 with Breast Cancer among Iranian-Azeri Patients

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Cited by 11 publications
(5 citation statements)
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“…In the present study PIN3 Ins16bp polymorphism was not found to be associated with the risk of developing breast cancer. Similar to our results, no association of PIN3 Ins16bp polymorphism Sarika Sharma et al with risk of breast cancer was observed in Turkish (Akkiprik et al, 2009), Arabian (Alawadi et al, 2011) and Iranian (Pouladi et al, 2014) patients. In the present study higher frequency of A2A2 genotype was observed in the patients (7%) as compared to the controls (4%) but the results were not statistically significant.…”
Section: Discussionsupporting
confidence: 90%
“…In the present study PIN3 Ins16bp polymorphism was not found to be associated with the risk of developing breast cancer. Similar to our results, no association of PIN3 Ins16bp polymorphism Sarika Sharma et al with risk of breast cancer was observed in Turkish (Akkiprik et al, 2009), Arabian (Alawadi et al, 2011) and Iranian (Pouladi et al, 2014) patients. In the present study higher frequency of A2A2 genotype was observed in the patients (7%) as compared to the controls (4%) but the results were not statistically significant.…”
Section: Discussionsupporting
confidence: 90%
“…In this study, an increased frequency of the A2 allele (21.7%) was observed in Malian population, suggesting that PIN3 16-bp polymorphism duplication of the TP53 gene is an important genetic marker for cancer in Malian population. This frequency was close to those observed in Morocco (19.3%) [20], Tunisia (22%) [36], Turkey (23%) [19] but different from those obtained in Germany (16%) [17], Portugal (16%) [18], India (19%) [23], the United States (14%) [23], Iran (55.2%) [41] and among an Arabic population (30.8%) [28]. This disparity in the distribution of allelic frequency in the general population may also be due to the sample size, ethnic origin and geographic location.…”
Section: Discussionsupporting
confidence: 89%
“…During past decades, numbers of genetic polymorphism in p53 locus have been widely investigated fo their effect in different cancer risks (Liu et al, 2014;Rao et al, 2014;Pouladi et al, 2014), among them the most common polymorphism is at codon 72 (Arg72Pro) (G>C) (rs1042522) This codon which is found at exon 4 of the p53 gene and is frequently studied worldwide (Vijayaraman et al, 2012;Xiang et al, 2012;Kafshdooz et al, 2014). At codon 72, arginine to proline substitution altered the p53 gene translation product, resulted in a reduced capacity of DNA repair, cell cycle regulation, apoptosis and thereby increased the susceptibility of cancer risk (Grochola et al, 2010).…”
Section: No Evidence Of Association Of the Arg72pro P53 Genementioning
confidence: 99%