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首页> 外文期刊>The Prostate >Genome-wide linkage scan for prostate cancer aggressiveness loci using families from the University of Michigan Prostate Cancer Genetics Project.
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Genome-wide linkage scan for prostate cancer aggressiveness loci using families from the University of Michigan Prostate Cancer Genetics Project.

机译:使用来自密歇根大学前列腺癌遗传学项目的家庭进行全基因组连锁扫描以检测前列腺癌的侵袭性位点。

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BACKGROUND: Prostate cancer (PC) is a complex disease that displays variable disease outcome, ranging from a relatively indolent disease to forms that result in death from the disease. One measure of disease severity is the Gleason score. Using the Gleason score as a measure of tumor aggressiveness, several independent genome scans have reported evidence of linkage. As of yet, however, no genes have been implicated. METHODS: We report an independent genome scan using the Gleason score as a quantitative trait. We genotyped 405 highly polymorphic microsatellite markers in 175 brother pairs from 103 families. RESULTS: Our strongest evidence of linkage is to 6q23 at 137 cM (D6S292, P = 0.0009). Other interesting regions (P < 0.005) were on chromosome 1p13-q21 and on chromosome 5p13-q11. CONCLUSIONS: Our results provide further evidence that tumor aggressiveness has a genetic component, and that this genetic component may be influenced by several independent genes.
机译:背景:前列腺癌(PC)是一种复杂的疾病,表现出可变的疾病结果,范围从相对惰性的疾病到导致疾病死亡的形式。疾病严重程度的一种度量是格里森评分。使用格里森评分作为衡量肿瘤侵袭性的指标,几项独立的基因组扫描报告了有关联的证据。但是,到目前为止,尚未涉及任何基因。方法:我们报告了使用格里森评分作为定量特征的独立基因组扫描。我们对来自103个家庭的175个兄弟对中的405个高度多态性微卫星标记进行了基因分型。结果:我们最有力的证据是在137 cM时与6q23连锁(D6S292,P = 0.0009)。其他有趣的区域(P <0.005)在1p13-q21染色体和5p13-q11染色体上。结论:我们的结果提供了进一步的证据,表明肿瘤的侵袭性具有遗传成分,并且该遗传成分可能受到几个独立基因的影响。

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