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p21 gene codon 31 arginine/serine polymorphism: Non-association with endometriosis

✍ Scribed by Yao-Yuan Hsieh; Fuu-Jen Tsai; Chi-Chen Chang; Wen-Chi Chen; Chang-Hai Tsai; Horng-Der Tsai; Cheng-Chieh Lin


Publisher
John Wiley and Sons
Year
2001
Tongue
English
Weight
25 KB
Volume
15
Category
Article
ISSN
0887-8013

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✦ Synopsis


Abstract

p21, an important regulator of the cell cycle, acts as a mediator of the growth‐suppressing and ‐promoting functions of p53. We aimed to investigate the association between codon 31 polymorphisms of p21 gene and endometriosis. Women were divided into two groups: endometriosis (n = 102) and nonendometriosis (n = 119). The gene polymorphism for p21 codon 31 involved a base change from AGC to AGA and amino acid changes from serine (Ser) to arginine (Arg). Polymorphisms (Ser homozygotes, heterozygotes, Arg homozygotes) between both groups were detected and compared. Associations between the endometriosis and polymorphisms were evaluated. The results revealed that the distributions of different p21 polymorphisms in both groups were nonsignificantly different. The proportions of Ser homozygote/heterozygote/Arg homozygote in endometriosis and nonendometriois populations were 26.5/48.0/25.5% and 17.6/50.4/31.9%, respectively. We concluded the noncorrelation between the endometriosis and the p21 codon 31 polymorphism. p21 gene codon 31 arginine/serine polymorphism is not a useful marker for prediction of endometriosis susceptibility. J. Clin. Lab. Anal. 15:184–187, 2001. © 2001 Wiley‐Liss, Inc.


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✍ Ming-Hsui Tsai; Wen-Chi Chen; Fuu-Jen Tsai 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 48 KB

## Abstract Background p21 (WAF1/CIP1) is a downstream protein from p53 and can arrest the cell cycle at the G1/S phase in response to signal from p53. The most frequently seen polymorphic site is at codon 31, where a base change from AGC to AGA causes an amino acid change from serine to arginine.