Dingli David, Traulsen Arne, Michor Franziska
Program for Evolutionary Dynamics, Harvard University, Cambridge, Massachusetts, United States of America.
PLoS Comput Biol. 2007 Mar 16;3(3):e53. doi: 10.1371/journal.pcbi.0030053. Epub 2007 Feb 1.
Most tissues in metazoans undergo continuous turnover due to cell death or epithelial shedding. Since cellular replication is associated with an inherent risk of mutagenesis, tissues are maintained by a small group of stem cells (SCs) that replicate slowly to maintain their own population and that give rise to differentiated cells. There is increasing evidence that many tumors are also maintained by a small population of cancer stem cells that may arise by mutations from normal SCs. SC replication can be either symmetric or asymmetric. The former can lead to expansion of the SC pool. We describe a simple model to evaluate the impact of (a)symmetric SC replication on the expansion of mutant SCs and to show that mutations that increase the probability of asymmetric replication can lead to rapid mutant SC expansion in the absence of a selective fitness advantage. Mutations in several genes can lead to this process and may be at the root of the carcinogenic process.
后生动物的大多数组织会因细胞死亡或上皮脱落而持续更新。由于细胞复制与诱变的内在风险相关,组织由一小群干细胞(SCs)维持,这些干细胞缓慢复制以维持自身数量,并产生分化细胞。越来越多的证据表明,许多肿瘤也由一小群癌症干细胞维持,这些癌症干细胞可能由正常干细胞的突变产生。干细胞复制可以是对称的,也可以是非对称的。前者可导致干细胞库的扩大。我们描述了一个简单的模型,以评估(非)对称干细胞复制对突变干细胞扩增的影响,并表明在没有选择性适应性优势的情况下,增加不对称复制概率的突变可导致突变干细胞快速扩增。几个基因的突变可导致这一过程,可能是致癌过程的根源。