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首页> 外文期刊>Clinical chemistry and laboratory medicine: CCLM >Detection of frequent ABCB1 polymorphisms by high-resolution melting curve analysis and their effect on breast carcinoma prognosis.
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Detection of frequent ABCB1 polymorphisms by high-resolution melting curve analysis and their effect on breast carcinoma prognosis.

机译:通过高分辨率熔解曲线分析检测频繁的ABCB1多态性及其对乳腺癌预后的影响。

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The ABCB1 gene encodes P-glycoprotein implicated in the development of cellular drug resistance. The aim of this study was to develop high-resolution melting (HRM) analysis for determination of ABCB1 polymorphisms and evaluate their associations with clinical data of breast carcinoma patients.HRM analysis was designed to assess five single nucleotide polymorphisms (SNPs) in ABCB1 (rs2214102, rs1128503, rs2032582, rs2032583 and rs1045642) in genomic DNA from 103 breast carcinoma patients. Results were confirmed by direct DNA sequencing.HRM analysis revealed distinct patterns of melting curves for the respective genotypes of all followed SNPs. Sensitivity of HRM analysis compared with direct DNA sequencing was superior (97.1% vs. 93.9%). The overall accuracy of HRM was 97.6%. The coefficients of variation in replicate experiments encompassed the range 0.002%-0.038%. On the basis of the examined SNPs, one strong haplotype block containing rs2032582 and rs1128503 SNPs was identified. Significant associations of rs2032582 SNP with tumor size, negative HER-2eu status, and family history of breast carcinoma were found. Patients carrying the ancestral homozygous genotype (GG) in rs2214102 had significantly worse progression-free survival in comparison with carriers of the non-ancestral allele (A) in the adjuvant set (p=0.005).A rapid, accurate, low-cost and time-effective method for screening ABCB1 SNPs was developed. Significant associations of ABCB1 rs2032582 and rs2214102 SNPs with prognostic factors and survival of patients were found.
机译:ABCB1基因编码参与细胞抗药性发展的P-糖蛋白。这项研究的目的是开发高分辨率熔解(HRM)分析以确定ABCB1多态性,并评估其与乳腺癌患者临床数据的关联性.HRM分析旨在评估ABCB1中的五个单核苷酸多态性(SNP)(rs2214102 ,rs1128503,rs2032582,rs2032583和rs1045642)来自103位乳腺癌患者的基因组DNA。通过直接DNA测序证实了结果.HRM分析揭示了所有随后SNP各自基因型的熔解曲线的不同模式。与直接DNA测序相比,HRM分析的灵敏度更高(分别为97.1%和93.9%)。 HRM的总体准确性为97.6%。复制实验中的变异系数范围为0.002%-0.038%。基于所检查的SNP,鉴定出一种包含rs2032582和rs1128503 SNP的强单倍型模块。发现rs2032582 SNP与肿瘤大小,HER-2 / neu阴性和乳腺癌家族史有显着相关性。与佐剂组中的非祖先等位基因(A)的携带者相比,rs2214102中携带祖先纯合基因型(GG)的患者的无进展生存期显着更差(p = 0.005)。开发了一种有效的方法来筛选ABCB1 SNP。发现ABCB1 rs2032582和rs2214102 SNP与患者的预后因素和生存率显着相关。

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