No associations of p73 G4C14-to-A4T14 at exon 2 and p53 Arg72Pro polymorphisms with the risk of digestive tract cancers in Japanese

被引:94
作者
Hamajima, N
Matsuo, K
Suzuki, T
Nakamura, T
Matsuura, A
Hatooka, S
Shinoda, M
Kodera, Y
Yamamura, Y
Hirai, T
Kato, T
Tajima, K
机构
[1] Aichi Canc Ctr, Res Inst, Div Epidemiol & Prevent, Chikusa Ku, Nagoya, Aichi 4648681, Japan
[2] Aichi Canc Ctr Hosp, Dept Gastroenterol, Nagoya, Aichi 4648681, Japan
[3] Aichi Canc Ctr Hosp, Dept Surg, Nagoya, Aichi 4648681, Japan
关键词
p73 dinucleotide polymorphism; p53 Arg72Pro polymorphism; esophageal cancer risks; stomach cancer risk; colorectal cancer risk; polymerase chain reaction with confronting two-pair primers;
D O I
10.1016/S0304-3835(02)00041-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A case-control study was conducted to examine the possible association between digestive tract cancers and p73 G4C14-to-A4TI4 at exon 2 and p53 Arg72Pro polymorphisms in Japanese. Cases were 102 esophageal cancer patients, 144 stomach cancer patients, and 147 colorectal cancer patients, and controls were 241 non-cancer outpatients. The genotype frequencies among controls were 55.3% for p73 GG at position 4, 40.4% for GA, and 4.3% for AA, and 37.7% for p53 ArgArg, 44.4% for ArgPro, and 18.0% for ProPro. No significant differences in the genotype frequencies were observed between the controls and each case group or case, as a whole. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:81 / 85
页数:5
相关论文
共 15 条
[1]   Molecular alterations of p73 in human esophageal squamous cell carcinomas:: loss of heterozygosity occurs frequently;: loss of imprinting and elevation of p73 expression may be related to defective p53 [J].
Cai, YYC ;
Yang, GY ;
Nie, Y ;
Wang, LD ;
Zhao, X ;
Song, YL ;
Seril, DN ;
Liao, J ;
Xing, EP ;
Yang, CS .
CARCINOGENESIS, 2000, 21 (04) :683-689
[2]   p73 [J].
Davis, PK ;
Dowdy, SF .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2001, 33 (10) :935-939
[3]   Polymerase chain reaction with confronting two-pair primers for polymorphism genotyping [J].
Hamajima, N ;
Saito, T ;
Matsuo, K ;
Kozaki, K ;
Takahashi, T ;
Tajima, K .
JAPANESE JOURNAL OF CANCER RESEARCH, 2000, 91 (09) :865-868
[4]  
Hamajima N, 2001, J Epidemiol, V11, P204
[5]  
HAMAJIMA N, 2001, CORRECTIONS, V11, P288
[6]  
Hamajima Nobuyuki, 2001, Asian Pac J Cancer Prev, V2, P99
[7]   Monoallelically expressed gene related to p53 at 1p36, a region frequently deleted in neuroblastoma and other human cancers [J].
Kaghad, M ;
Bonnet, H ;
Yang, A ;
Creancier, L ;
Biscan, JC ;
Valent, A ;
Minty, A ;
Chalon, P ;
Lelias, JM ;
Dumont, X ;
Ferrara, P ;
McKeon, F ;
Caput, D .
CELL, 1997, 90 (04) :809-819
[8]   Expression of p73 in colorectal carcinoma: Clinicopathological relevance [J].
Liu, L ;
Cui, X ;
Sakaguchi, T ;
Sasaki, M ;
Suda, T ;
Hatakeyama, K .
JOURNAL OF INTERNATIONAL MEDICAL RESEARCH, 2001, 29 (04) :297-303
[9]   Maintaining imprinting [J].
Mann, MRW ;
Bartolomei, MS .
NATURE GENETICS, 2000, 25 (01) :4-5
[10]  
Nomoto S, 1998, CANCER RES, V58, P1380