Horwitz M
Markey Molecular Medicine Center, Department of Medicine, University of Washington, Seattle 98195-7720, USA.
Leukemia. 1997 Aug;11(8):1347-59. doi: 10.1038/sj.leu.2400707.
Familial leukemia is rare, but, as is the case with other cancer family syndromes, its study is likely to lead to the identification of genes causative of the far more common, sporadic cases. I review the clinical and, what is known of the molecular genetic features of familial leukemia. I propose a nosology based on whether the leukemia is a component of a medical syndrome or exists as a solitary disease, the apparent mode of inheritance, and the distribution of leukemia types and subtypes in affected family members. I review the recent findings from my group that leukemia is inherited with 'anticipation', in the form of a declining age of onset with each passing generation. I consider two models of leukemia genesis that can potentially account for anticipation in familial cases and incorporate epidemiological observations made in sporadic cases. The first model is analogous to trinucleotide repeat expansion in Huntington disease, myotonic dystrophy, and other inherited neurodegenerative illness demonstrating anticipation. The second model considers evidence that anticipation may be common to multiple types of familial cancer and is based on the intergenerational inheritance of multiple downstream mutations resulting from a defect in a single DNA repair gene.
家族性白血病较为罕见,但是,与其他癌症家族综合征一样,对其进行研究可能会促使人们识别出那些在更为常见的散发性病例中致病的基因。我回顾了家族性白血病的临床特征以及已知的分子遗传学特征。我提出了一种疾病分类法,该分类法基于白血病是某种医学综合征的一部分还是作为一种孤立疾病存在、明显的遗传模式以及白血病类型和亚型在受影响家庭成员中的分布情况。我回顾了我的团队最近的研究发现,即白血病以“遗传早现”的方式遗传,表现为每一代发病年龄逐渐降低。我考虑了两种白血病发生模型,这两种模型有可能解释家族性病例中的遗传早现现象,并纳入了散发性病例中的流行病学观察结果。第一种模型类似于亨廷顿舞蹈症、强直性肌营养不良以及其他表现出遗传早现现象的遗传性神经退行性疾病中的三核苷酸重复扩增。第二种模型考虑到有证据表明遗传早现现象可能在多种类型的家族性癌症中普遍存在,并且基于单个DNA修复基因缺陷导致的多个下游突变的代际遗传。