McIndoe R A, Stanford J L, Gibbs M, Jarvik G P, Brandzel S, Neal C L, Li S, Gammack J T, Gay A A, Goode E L, Hood L, Ostrander E A
Department of Molecular Biotechnology, University of Washington, Seattle, USA.
Am J Hum Genet. 1997 Aug;61(2):347-53. doi: 10.1086/514853.
Linkage of a putative prostate cancer-susceptibility locus (HPC1) to chromosome 1q24-25 has recently been reported. Confirmation of this linkage in independent data sets is essential because of the complex nature of this disease. Here we report the results of a linkage analysis using 10 polymorphic markers spanning approximately 37 cM in the region of the putative HPC1 locus in 49 high-risk prostate cancer families. Data were analyzed by use of two parametric models and a nonparametric method. For the parametric LOD-score method, the first model was identical to the original report by Smith and coworkers ("Hopkins"), and the second was based on a segregation analysis previously reported by Carter and coworkers ("Seattle"). In both cases, our results do not confirm the linkage reported for this region. Calculated LOD scores from the two-point analysis for each marker were highly negative at small recombination fractions. Multipoint LOD scores for this linkage group were also highly negative. Additionally, we were unable to demonstrate heterogeneity within the data set, using HOMOG. Although these data do not formally exclude linkage of a prostate cancer-susceptibility locus at HPC1, it is likely that other prostate cancer-susceptibility loci play a more critical role in the families that we studied.
最近有报道称,一个假定的前列腺癌易感基因座(HPC1)与1号染色体1q24 - 25区域存在连锁关系。鉴于这种疾病的复杂性,在独立数据集中证实这种连锁关系至关重要。在此,我们报告了一项连锁分析的结果,该分析使用了10个多态性标记,这些标记跨越假定的HPC1基因座区域约37厘摩,涉及49个高危前列腺癌家族。数据通过两种参数模型和一种非参数方法进行分析。对于参数LOD评分法,第一个模型与Smith及其同事最初的报告(“霍普金斯”)相同,第二个模型基于Carter及其同事先前报告的分离分析(“西雅图”)。在这两种情况下,我们的结果均未证实该区域所报告的连锁关系。每个标记的两点分析计算出的LOD评分在小重组率时均为高度负值。该连锁组的多点LOD评分也为高度负值。此外,我们使用HOMOG未能证明数据集中存在异质性。尽管这些数据并未正式排除HPC1处前列腺癌易感基因座的连锁关系,但在我们研究的家族中,其他前列腺癌易感基因座可能发挥着更关键的作用。