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Linkage analyses at the chromosome 1 loci 1q24-25 (HPC1), 1q42.2-43 (PCAP), and 1p36 (CAPB) in families with hereditary prostate cancer

机译:遗传性前列腺癌家系染色体1位点1q24-25(HpC1),1q42.2-43(pCap)和1p36(CapB)的连锁分析

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摘要

Recent studies suggest that hereditary prostate cancer (PRCA) is a complex disease, involving multiple susceptibility genes and variable phenotypic expression. Through linkage analysis, potential prostate cancer susceptibility loci have been mapped to 3 regions on chromosome 1. To investigate the reported linkage to these regions, we conducted linkage studies on 144 PRCA families by using microsatellite markers in regions 1q2425 (HPC1) and 1q42.2-43 (PCAP). We also examined the 1p36 (CAPB) region in 13 PRCA families with at least one case of brain cancer. No significant evidence of linkage to the HPC1 or PCAP region was found when the entire data set was analyzed. However, weak evidence for linkage to HPC1 was observed in the subset of families with male-to-male transmission (n = 102; maximum multipoint nonparametric linkage [NPL] 1.99, P = .03). Weak evidence for linkage with heterogeneity within this subset was also observed (HLOD 1.21, P = .02), with ~20% of families linked. Although not statistically significant, suggestive evidence for linkage to PCAP was observed for the families (n = 21) that met the three criteria of male-to-male transmission, average age of diagnosis
机译:最近的研究表明,遗传性前列腺癌(PRCA)是一种复杂的疾病,涉及多个易感基因和可变的表型表达。通过连锁分析,潜在的前列腺癌易感基因座已定位到1号染色体上的3个区域。为了研究与这些区域的连锁,我们使用1q2425(HPC1)和1q42.2区域的微卫星标记对144个PRCA家族进行了连锁研究。 -43(PCAP)。我们还检查了13个患有至少一例脑癌的PRCA家庭中的1p36(CAPB)区域。分析整个数据集时,未发现与HPC1或PCAP区域相关的重要证据。但是,在以男性对男性传播的家庭子集中观察到与HPC1连锁的证据不充分(n = 102;最大多点非参数连锁[NPL] 1.99,P = .03)。还观察到与该子集内的异质性相关联的证据不足(HLOD 1.21,P = .02),约有20%的家庭关联。尽管在统计学上不显着,但在满足男性对男性传播的三个标准,平均诊断年龄的家庭(n = 21)中观察到了与PCAP连锁的暗示性证据。

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