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非裔美国家庭中的遗传性前列腺癌:使用定位到五个候选易感基因座的标记进行连锁分析。

Hereditary prostate cancer in African American families: linkage analysis using markers that map to five candidate susceptibility loci.

作者信息

Brown W M, Lange E M, Chen H, Zheng S L, Chang B, Wiley K E, Isaacs S D, Walsh P C, Isaacs W B, Xu J, Cooney K A

机构信息

Department of Public Health Sciences, Wake Forest University School of Medicine, Winston-Salem, NC 27157, USA.

出版信息

Br J Cancer. 2004 Jan 26;90(2):510-4. doi: 10.1038/sj.bjc.6601417.

DOI:10.1038/sj.bjc.6601417
PMID:14735201
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2410149/
Abstract

African American men have the highest incidence of prostate cancer in the world. Despite this statistic, linkage studies designed to localise prostate cancer susceptibility alleles have included primarily men of Caucasian descent. In this report, we performed a linkage analysis using 33 African American prostate cancer families from two independent research groups. In total, 126 individuals (including 89 men with prostate cancer) were genotyped using markers that map to five prostate cancer susceptibility loci, namely HPC1 at 1q24-25, PCAP at 1q42.2-43, CAPB at 1p36, HPC20 on chromosome 20, and HPCX at Xq27-28. Multipoint mode-of-inheritance-free linkage analyses were performed using the GENEHUNTER software. Some evidence of prostate cancer was detected to HPC1 using all families with a maximum NPL Z score of 1.12 near marker D1S413 (P=0.13). Increased evidence of linkage was observed in the 24 families with prostate cancer diagnosis prior to age 65 years and in the 20 families with male-to-male transmission. Some evidence of prostate cancer linkage was also detected at markers mapping to PCAP, HPC20, and HPCX. Continued collection and analysis of African American prostate cancer families will lead to an improved understanding of inherited susceptibility in this high-risk group.

摘要

非裔美国男性是全球前列腺癌发病率最高的人群。尽管有这一统计数据,但旨在定位前列腺癌易感等位基因的连锁研究主要纳入的是白种人后裔男性。在本报告中,我们使用来自两个独立研究小组的33个非裔美国前列腺癌家族进行了连锁分析。总共126名个体(包括89名前列腺癌男性患者)使用定位到五个前列腺癌易感位点的标记进行了基因分型,这五个位点分别是位于1q24 - 25的HPC1、位于1q42.2 - 43的PCAP、位于1p36的CAPB、位于20号染色体上的HPC20以及位于Xq27 - 28的HPCX。使用GENEHUNTER软件进行了多点无遗传模式连锁分析。在所有家族中,检测到一些前列腺癌与HPC1的关联证据,在标记D1S413附近最大NPL Z评分为1.12(P = 0.13)。在65岁之前被诊断为前列腺癌的24个家族以及存在男性对男性遗传的20个家族中,观察到连锁证据增加。在定位到PCAP、HPC20和HPCX的标记处也检测到一些前列腺癌连锁的证据。持续收集和分析非裔美国前列腺癌家族将有助于更好地理解这个高危群体的遗传易感性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba82/2410149/fcf67ed8b33b/90-6601417f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba82/2410149/fcf67ed8b33b/90-6601417f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba82/2410149/fcf67ed8b33b/90-6601417f1.jpg

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Linkage of prostate cancer susceptibility loci to chromosome 1.前列腺癌易感基因座与1号染色体的连锁关系。
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PCAP is the major known prostate cancer predisposing locus in families from south and west Europe.PCAP是来自南欧和西欧家族中已知的主要前列腺癌易感基因座。
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Am J Hum Genet. 2000 Feb;66(2):539-46. doi: 10.1086/302771.