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    Please use this identifier to cite or link to this item: http://asiair.asia.edu.tw/ir/handle/310904400/100183


    Title: Significant Association of Interleukin-10 Polymorphisms with Childhood Leukemia Susceptibility in Taiwan
    Authors: 羅文吉;LO, WEN-JYI;CHA, WEN-SHIN;CHANG, WEN-SHIN;HSU, HAN-FANG;HSU, HAN-FANG;JI, HONG-XUE;JI, HONG-XUE;HS, CHIEH-LUN;HSIAO, CHIEH-LUN;TSA, CHIA-WEN;TSAI, CHIA-WEN;YEH, SU-PENG;YEH, SU-PENG;CHE, CHUAN-MU;CHEN, CHUAN-MU;包大?;Bau, Da-Tian;*
    Contributors: 生物資訊與醫學工程學系
    Date: 2016-05
    Issue Date: 2016-08-08 14:39:10 (UTC+8)
    Abstract: Mounting evidence supports the notion that inflammatory processes play a role in carcinogenesis, and interleukin-10 (IL10) is an important inflammatory cytokine. This study aimed to evaluate the contribution of IL10 A-1082G (rs1800896), T-819C (rs3021097) and A-592C (rs1800872) genotypes to the risk of childhood acute lymphoblastic leukemia (ALL) in Taiwan. Associations of these IL10 polymorphic genotypes with ALL risk were analyzed in 266 patients with childhood ALL patients and 266 non-cancer healthy controls by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) methodology. The results showed that CC genotype carriers at IL10 T-819C were at lower risk for childhood ALL (odds ratio=0.33, 95% confidence interval=0.16-0.68). On the contrary, AC and CC genotype carriers at IL10 A-592C were at higher risk for childhood ALL (odds ratio=1.73 and 6.34, 95% confidence interval=1.19-2.51 and 3.16-12.72, respectively). There was no difference in the distribution of A-1082G genotypes between childhood ALL and control groups. The genotypes at IL10 T-819C and A-592C may serve as predictive biomarkers for childhood ALL in Taiwan.
    Relation: IN VIVO
    Appears in Collections:[生物資訊與醫學工程學系 ] 期刊論文

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