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Somatic mutations and the hierarchy of hematopoiesis

机译:体细胞突变和造血系统的层次

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摘要

Clonal disease is often regarded as almost synonymous with cancer. However, it is becoming increasingly clear that our bodies harbor numerous mutant clones that are not tumors, and mostly give rise to no disease at all. Here we discuss three somatic mutations arising within the hematopoietic system: BCR-ABL, characteristic of chronic myeloid leukemia; mutations of the PIG-A gene, characteristic of paroxysmal nocturnal hemoglobinuria; the V617F mutation in the JAK2 gene, characteristic of myeloproliferative diseases. The population frequencies of these three blood disorders fit well with a hierarchical model of hematopoiesis. The fate of any mutant clone will depend on the target cell and on the fitness advantage, if any, that the mutation confers on the cell. In general, we can expect that only a mutation in a hematopoietic stem cell will give long-term disease; the same mutation taking place in a cell located more downstream may produce just a ripple in the hematopoietic ocean.
机译:克隆疾病通常被认为是癌症的同义词。但是,越来越清楚的是,我们的身体中藏有许多不是肿瘤的突变克隆,并且几乎根本没有任何疾病。在这里,我们讨论在造血系统内发生的三种体细胞突变:BCR-ABL,慢性粒细胞白血病的特征; PIG-A基因突变,表现为阵发性夜间血红蛋白尿; JAK2基因中的V617F突变是骨髓增生性疾病的特征。这三种血液疾病的人群频率与造血系统的分层模型非常吻合。任何突变克隆的命运将取决于靶细胞以及该突变赋予细胞的适应性优势(如果有)。通常,我们可以预期,造血干细胞中只有突变会导致长期疾病。在位于更下游的细胞中发生的相同突变可能只会在造血海洋中产生波纹。

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