Peltomäki P, Aaltonen L A, Sistonen P, Pylkkänen L, Mecklin J P, Järvinen H, Green J S, Jass J R, Weber J L, Leach F S
Department of Medical Genetics, University of Helsinki, Finland.
Science. 1993 May 7;260(5109):810-2. doi: 10.1126/science.8484120.
Genetic linkage analysis was used to determine whether a specific chromosomal locus could be implicated in families with a history of early onset cancer but with no other unique features. Close linkage of disease to anonymous microsatellite markers on chromosome 2 was demonstrated in two large kindreds. The pairwise lod scores for linkage to marker D2S123 in these kindreds were 6.39 and 1.45 at zero recombination, and multipoint linkage with flanking markers resulted in lod scores of 6.47 and 6.01. These results prove the existence of a genetically determined predisposition to colorectal cancer that has important ramifications for understanding and preventing this disease.
遗传连锁分析用于确定在有早发性癌症家族史但无其他独特特征的家庭中,特定染色体位点是否与之相关。在两个大家族中证实了疾病与2号染色体上匿名微卫星标记的紧密连锁。在这些家族中,与标记D2S123连锁的成对对数优势分数在零重组时分别为6.39和1.45,与侧翼标记的多点连锁导致对数优势分数分别为6.47和6.01。这些结果证明存在一种由遗传决定的结直肠癌易感性,这对理解和预防这种疾病具有重要意义。