Miller David C, Zheng S Lilly, Dunn Rodney L, Sarma Aruna V, Montie James E, Lange Ethan M, Meyers Deborah A, Xu Jianfeng, Cooney Kathleen A
Department of Urology, University of Michigan, Medical School, Ann Arbor, Michigan 48109-0946, USA.
Cancer Res. 2003 Jul 1;63(13):3486-9.
Both rare germ-line mutations and common sequence variants of the macrophage scavenger receptor 1 (MSR1) gene have recently been implicated as potential prostate cancer susceptibility factors. However, existing studies are limited by the referral-based nature of samples and a paucity of African-American participants. In this context, we evaluated the association of germ-line mutations and common MSR1 sequence variants with prostate cancer risk in a case control study of a community-based sample of 134 African-American men with prostate cancer and 340 unaffected controls. In our sample, the rare Asp174Tyr missense change was identified nearly twice as frequently in men with prostate cancer (6.8%) compared with unaffected controls (3.6%; P = 0.14). Moreover, significantly different allele frequencies between cases and controls were observed for one of the sequence variants, IVS5-59 (P = 0.02). Taken together, our results provide some additional support for the hypothesis that selected, rare MSR1 mutations are associated with increased prostate cancer susceptibility among African-American men.
巨噬细胞清道夫受体1(MSR1)基因的罕见种系突变和常见序列变异最近都被认为是潜在的前列腺癌易感因素。然而,现有研究受到样本基于转诊性质的限制,且非裔美国参与者较少。在此背景下,我们在一项病例对照研究中评估了种系突变和常见MSR1序列变异与前列腺癌风险的关联,该研究以一个基于社区的样本为基础,包括134名患有前列腺癌的非裔美国男性和340名未受影响的对照。在我们的样本中,与未受影响的对照(3.6%;P = 0.14)相比,在患有前列腺癌的男性中,罕见的Asp174Tyr错义变化的检出频率几乎高出一倍(6.8%)。此外,对于其中一个序列变异IVS5 - 59,病例组和对照组之间观察到显著不同的等位基因频率(P = 0.02)。综合来看,我们的结果为以下假设提供了一些额外支持:特定的罕见MSR1突变与非裔美国男性前列腺癌易感性增加有关。