| Autor: |
Asadian, Fatemeh, Ghadyani, Mohammadamin, Antikchi, Mohamad Hossein, Dastgheib, Seyed Alireza, Neamatzadeh, Hossein, Sheikhpour, Elnaz, Khajehnoori, Sahel, Tabei, Seyed Sajjad |
| Zdroj: |
Journal of Gastrointestinal Cancer; Mar2022, Vol. 53 Issue 1, p78-83, 6p |
| Abstrakt: |
Background: Genetic polymorphisms play an important role in the development of colorectal cancer (CRC). Functional variants in the epidermal growth factor (EGF), survivin, and Ephrin A1 (EFNA1) genes have been previously reported to play a potential role in susceptibility to CRC, but these polymorphisms have not been well replicated. The aim of this study was to assess the association of the EGF 61A>G, Survivin -31G>C, and EFNA1 -1732G>A polymorphisms with the susceptibility to CRC in an Iranian population. Methods: A total of 148 cases diagnosed with CRC and 160 healthy subjects were recruited. The EGF 61A>G, survivin -31G>C, and EFNA1 -1732G>A polymorphisms were genotyped using a polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) assay. Results: Our data revealed that the homozygous mutant genotype (CC: OR = 2.895, 95% CI = 1.092–7.673, p = 0.033) and mutant allele (C: OR = 1.629, 95% CI = 1.152–2.303, p = 0.006) of the survivin -31G>C were associated with an increased risk of CRC in the Iranian population. However, our results failed to show an association between the EGF 61A>G and EFNA1 -1732G>A polymorphisms and CRC risk. Conclusion: Our results revealed that the survivin -31G>C polymorphism might play an important role in development of CRC in Iranian population. However, no association of EGF 61A>G and EFNA1 -1732G>A polymorphisms with CRC risk was found. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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