Distribution of a single nucleotide polymorphism of insulin-like growth factor-1 in colorectal cancer patients and its association with mucinous adenocarcinoma

被引:5
作者
Lin, Jen-Kou [1 ]
Shen, Ming-Yin [2 ]
Lin, Tzu-Chen [1 ]
Lan, Yuan-Tzu [1 ]
Wang, Huann-Sheng [1 ]
Yang, Shung-Haur [1 ]
Li, Anna Fen-Yau [3 ]
Chang, Shih-Ching [1 ]
机构
[1] Natl Yang Ming Univ, Taipei Vet Gen Hosp, Div Colon & Rectal Surg, Dept Surg, Taipei 11217, Taiwan
[2] Hsinchu Gen Hosp, Dept Surg, Hsinchu, Taiwan
[3] Natl Yang Ming Univ, Taipei Vet Gen Hosp, Dept Pathol, Taipei 11217, Taiwan
关键词
IGF-1; Colorectal cancer; Polymorphism; Age; IGF-I; CIRCULATING LEVELS; GENE POLYMORPHISM; FACTOR SYSTEM; COLON; RISK; EXPRESSION; RESISTANCE; ONSET;
D O I
10.5301/JBM.2010.6119
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Purpose: To analyze the difference in the distribution of an insulin growth factor-1 (IGF-1) polymorphism (-2995 C/A) between young and old colorectal cancer (CRC) patients. Methods: Information from 950 CRC patients undergoing surgery at the Taipei Veterans General Hospital between 2000 and 2005 was collected. The IGF-1 polymorphism was analyzed in patients in extreme age ranges at the time of CRC onset (i.e., under the 20th and above the 80th percentiles, respectively). Associations between clinicopathological variables and the IGF-1 polymorphism were analyzed. Results: Young CRC patients had a higher frequency of advanced disease (58.7%) and mucinous adenocarcinoma (20%) than old CRC patients. Among old CRC patients, the frequency of the AA genotype of IGF-1 was 12.7% (24/189), which was significantly higher than in young patients (4.2%). Other clinicopathological factors including tumor location, differentiation, lymphovascular invasion, and TNM stage were not associated with the AA genotype of IGF-1. Mucinous differentiation (but not the other clinicopathological factors) was significantly associated with the CA/AA genotype of IGF-1 (39/195). Conclusions: Older patients had a higher frequency of the AA genotype of IGF-1(-2995 C/A), while younger patients more often had advanced disease and mucinous adenocarcinoma.
引用
收藏
页码:195 / 199
页数:5
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