Kohonen-Corish M R, Doe W F, St John D J, Macrae F A
Division of Clinical Sciences, John Curtin School of Medical Research, Australian National University, Canberra.
J Gastroenterol Hepatol. 1995 Jan-Feb;10(1):76-80. doi: 10.1111/j.1440-1746.1995.tb01052.x.
Hereditary non-polyposis colon cancer (HNPCC) comprises 2-6% of the total colorectal cancer burden. Two families are described that show linkage between the HNPCC susceptibility gene and the markers D2S123 and D2S119 on chromosome 2p, producing multipoint lod scores of 3.62 and 3.83, respectively, in the largest pedigree. In our third family the multipoint lod scores for D2S123 and D2S119, -2.97 and -3.12, excluded localization of a susceptibility gene in this region indicating that there is at least one more gene that causes predisposition to HNPCC. The exclusion was based on at least one genotype for an individual who had multiple primary colon and extracolonic tumours and could not be considered to have had common forms of cancer. Our results therefore encourage further gene mapping to pursue the localization of additional HNPCC genes. These findings confirm the presence of the susceptibility gene for HNPCC, COCA1, on chromosome 2p. They allow the immediate identification of a subset of HNPCC families, and provide the means for presymptomatic testing of family members if sufficient number of members are available for study.
遗传性非息肉病性结直肠癌(HNPCC)占结直肠癌总负担的2% - 6%。本文描述了两个家系,显示HNPCC易感基因与2号染色体短臂上的标记D2S123和D2S119之间存在连锁关系,在最大的家系中,多点对数优势比分(lod score)分别为3.62和3.83。在我们的第三个家系中,D2S123和D2S119的多点对数优势比分别为 - 2.97和 - 3.12,排除了该区域存在易感基因的可能性,这表明至少还有一个基因会导致HNPCC易感性。这种排除是基于一个患有多个原发性结肠癌和结肠外肿瘤且不能被认为患有常见癌症形式的个体的至少一种基因型。因此,我们的结果鼓励进一步进行基因定位,以寻找其他HNPCC基因的位置。这些发现证实了2号染色体短臂上存在HNPCC易感基因COCA1。它们使得能够立即识别出一部分HNPCC家系,并在有足够数量的家庭成员可供研究时,为家庭成员的症状前检测提供了方法。