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作 者:蒋东华[1] WILLIAM W Zhang 李霓[1] 周宝森[1]
机构地区:[1]中国医科大学公共卫生学院流行病学教研室,辽宁沈阳110001 [2]Center for Breast Cancer Research on Women's Health,Sunnybrook & Women's College Health Science Center,Toronto,M5G 1N8,Canada
出 处:《中华肿瘤防治杂志》2006年第21期1609-1613,共5页Chinese Journal of Cancer Prevention and Treatment
摘 要:目的:探讨细胞间黏附分子(ICAM)基因座位单核苷酸多态性(SNPs)与乳腺癌危险度之间的关系,以及这些SNPs位点与BRCA1基因相互作用对乳腺癌危险度的影响。方法:研究对象为1034例女性乳腺癌病例和1091例非恶性肿瘤对照。采外周血提DNA后使用基质辅助激光解吸附电离飞行时间质谱检测技术(MALDI-TOF)对SNPs位点进行基因分型。用χ2检验和Logistic回归模型进行统计学分析。结果:rs1056538位点携带C等位基因对个体患乳腺癌具有保护作用(ORCT=0.3423,95%CI:0.2351~0.4982;ORCC=0.5943,95%CI:0.3899~0.9058),而rs2228615AG和rs281439GG基因型个体则有较高的危险度发生乳腺癌(ORrs2228615AG=2.6771,95%CI:1.4938~4.7976;ORrs281439GG=1.9845,95%CI:1.0287~3.8285)。对于携带BRCA1突变的个体,与全部研究对象所得的结果相比,rs1056538位点携带C等位基因的保护作用更为明显(ORCT=0.2797,95%CI:0.1984~0.3321;ORCC=0.4983,95%CI:0.3942~0.7211),rs2228615位点携带G等位基因的危险度更高(ORAG=3.3369,95%CI:1.9195~5.8009;ORGG=2.0289,95%CI:1.1704~3.5170),而rs281439GG基因型危险度改变不大。结论:ICAM基因座位上SNPs与乳腺癌危险度有关。ICAM基因与BRCA1基因间存在相互作用,影响了乳腺癌的危险度。OBJECTIVE:To explore the associations between polymorphisms in ICAM gene locus and breast cancer risk,and the effect of interactions between SNPs and BRCA1 on breast cancer risk. METHODS: There were 1 034 breast cancer cases and 1 091 controls in this study. After DNA was isolated from peripheral blood, the matrix-assisted laser de sorption/ionization time-of-flight mass spectrometry (MALDI-TOF)was used to determine the genotype of every SNPs. χ^2 test and logistic regression model were used to.analyze the association. RESULTS: Rs1056538 with C allele might have some prevention effect on women breast cancer risk (ORCT=0.342 3, 95%CI: 0.235 1-0.498 2; ORCC= 0. 594 3, 95%CI: 0. 389 9-0. 905 8), while women whose genotype was rs2228615AG or rs281439GG would have higher breast cancer risk(OR rs2228615AG = 2. 677 1, 95% CI: 1.493 8-4.797 6; OR rs281439GG= 1.984 5, 95%CI: 1. 028 7-3. 828 5). For women with BRCA1 mutation, compared with the results of all subjects, rs1056538 with C allele might have greater prevention effect (ORCT = 0. 279 7, 95%CI: 0.198 4- 0.332 1; ORCC = 0.498 3, 95% CI: 0. 394 2-0. 721 1), while rs222861 with G allele would have higher breast cancer risk (ORAG = 3.336 9, 95% CI: 1.919 5-5.800 9; ORGG=2.028 9, 95%CI:1.170 4- 3. 517 0), but rs281439GG genotype had little diffenence in the effect on the risk. CONCLUSION: There is an association between ICAM gene locus SNPs and breast cancer risk. The interaction between ICAM gene and BRCA1 has some effect on breast cancer risk.
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