首页> 外文期刊>European journal of human genetics: EJHG >PCAP is the major known prostate cancer predisposing locus in families from south and west Europe.
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PCAP is the major known prostate cancer predisposing locus in families from south and west Europe.

机译:PCAP是南欧和西欧家庭中已知的主要前列腺癌易感基因。

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To date four prostate cancer predisposing loci have been mapped: HPC1 (Hereditary Prostate Cancer 1) on 1q24-25, PCaP (Predisposing for Cancer Prostate) on 1q42.2-43, CAPB (Cancer Prostate and Brain) on 1p36, and HPCX on Xq27-28. We examined evidence for linkage to those loci in 64 families from south and west Europe. Genotyping of three (six for PCaP) markers encompassing the candidate regions were performed on 221 individuals including 159 affected patients. The resulting data were analysed using both parametric and non parametric linkage methods. No significant evidence of linkage to HPC1, CAPB, or HPCX was found either in the whole population or when pedigrees were stratified according to criteria specific to each locus. By contrast, results in favour of linkage to PCaP locus were observed with maximum multipoint NPL and HLOD scores of 2.8 (P = 0.0026) and 2.65 respectively. Homogeneity analysis performed with multipoint LOD scores gave an estimated proportion of families with linkage to this locus up to 50%. Particularly, families with an earlier age at diagnosis (< or = 65-years-old) contributed significantly to the evidence of linkage with a maximum multipoint NPL score of 2.03 (P = 0.024). Those results suggest that PCaP is the most frequent known locus predisposing to hereditary prostate cancer cases from families from south and west Europe.
机译:迄今为止,已经绘制了四个前列腺癌易感基因座:1q24-25上的HPC1(遗传性前列腺癌1),1q42.2-43上的PCaP(癌症易感性),1p36上的CAPB(前列腺癌和脑癌)和HPCX上。 Xq27-28。我们检查了与南欧和西欧64个家庭的那些基因座相关的证据。在包括159名患病患者在内的221位个体上进行了涵盖候选区域的三个(针对PCaP为六个)标记的基因分型。使用参数和非参数链接方法对所得数据进行了分析。在整个人群中或根据针对每个基因座的特定标准对谱系进行分层时,均未发现与HPC1,CAPB或HPCX相关的重要证据。相比之下,观察到有利于与PCaP基因座连锁的结果,最大多点NPL和HLOD得分分别为2.8(P = 0.0026)和2.65。使用多点LOD评分进行的同质性分析估计,与该基因座相关联的家庭比例高达50%。特别是,诊断时年龄较早(<或= 65岁)的家庭以最大的多点不良贷款得分为2.03(P = 0.024)为连锁证据做出了重要贡献。这些结果表明,PCaP是来自南欧和西欧家庭的最常见的遗传性前列腺癌病例的诱因。

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