JaLCDOI |
10.18926/AMO/47013
|
フルテキストURL |
65_5_315.pdf
|
著者 |
Wang, Lei|
Kaku, Haruki|
Huang, Peng|
Xu, Kexin|
Yang, Kai|
Zhang, Jiheng|
Li, Ming|
Xie, Liping|
Wang, Xiaofeng|
Sakai, Akiko|
Watanabe, Masami|
Nasu, Yasutomo|
Shimizu, Kenji|
Kumon, Hiromi|
Na, Yanqun|
|
抄録 |
Deficiencies in the human DNA repair gene WRN are the cause of Werner syndrome, a rare autosomal recessive disorder characterized by premature aging and a predisposition to cancer. This study evaluated the association of WRN Leu1074Phe (rs1801195), a common missense single nucleotide polymorphism in WRN, with prostate cancer susceptibility in Chinese subjects. One hundred and forty-seven prostate cancer patients and 111 male cancer-free control subjects from 3 university hospitals in China were included. Blood samples were obtained from each subject, and the single nucleotide polymorphism WRN Leu1074Phe was genotyped by using a Snapshot assay. The results showed that WRN Leu1074Phe was associated with the risk of prostate cancer in Chinese men and that the TG/GG genotype displayed a decreased prevalence of prostate cancer compared with the TT genotype (OR=0.58, 95%CI:0.35-0.97, p=0.039). Through stratified analysis, more significant associations were revealed for the TG/GG genotype in the subgroup with diagnosis age <_ 72 yr (OR=0.27, 95%CI:0.12-0.61, p=0.002) and in patients with localized diseases (OR=0.36, 95%CI:0.19-0.70, p=0.003). However, no statistically significant difference was found in the subgroup with age >72 yr or in patients with advanced diseases. We concluded that the genetic variant Leu1074Phe in the DNA repair gene WRN might play a role in the risk of prostate cancer in Chinese subjects.
|
キーワード |
polymorphism
prostatic neoplasms
single nucleotide
susceptibility
WRN
|
Amo Type |
Original Article
|
発行日 |
2011-10
|
出版物タイトル |
Acta Medica Okayama
|
巻 |
65巻
|
号 |
5号
|
出版者 |
Okayama University Medical School
|
開始ページ |
315
|
終了ページ |
323
|
ISSN |
0386-300X
|
NCID |
AA00508441
|
資料タイプ |
学術雑誌論文
|
言語 |
English
|
著作権者 |
CopyrightⒸ 2011 by Okayama University Medical School
|
論文のバージョン |
publisher
|
査読 |
有り
|
PubMed ID |
22037267
|
Web of Sience KeyUT |
000296116400005
|