Ionizing radiation and hematopoietic malignancies Altering the adaptive landscape

被引:21
|
作者
Fleenor, Courtney J. [1 ,3 ]
Marusyk, Andriy [1 ,4 ]
DeGregori, James [1 ,2 ,3 ,4 ]
机构
[1] Univ Colorado, Denver Sch Med, Dept Biochem & Mol Genet, Aurora, CO USA
[2] Univ Colorado, Denver Sch Med, Dept Pediat, Aurora, CO USA
[3] Univ Colorado, Denver Sch Med, Integrated Dept Immunol, Aurora, CO USA
[4] Univ Colorado, Denver Sch Med, Program Mol Biol, Aurora, CO USA
关键词
Notch; p53; fitness; irradiation; hematopoietic; evolution; DNA-DAMAGE; STEM-CELLS; CANCER; NOTCH1; REPAIR; P53; TUMORIGENESIS; DEFICIENT; LEUKEMIA; OPINION;
D O I
10.4161/cc.9.15.12311
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Somatic evolution, which underlies tumor progression, is driven by two essential components: (1) diversification of phenotypes through heritable mutations and epigenetic changes and (2) selection for mutant clones which possess higher fitness. Exposure to ionizing radiation (IR) is highly associated with increased risk of carcinogenesis. This link is traditionally attributed to causation of oncogenic mutations through the mutagenic effects of irradiation. On the other hand, potential effects of irradiation on altering fitness and increasing selection for mutant clones are frequently ignored. Recent studies bring the effects of irradiation on fitness and selection into focus, demonstrating that IR exposure results in stable reductions in the fitness of hematopoietic stem and progenitor cell populations. These reductions of fitness are associated with alteration of the adaptive landscape, increasing the selective advantages conferred by certain oncogenic mutations. Therefore, the link between irradiation and carcinogenesis might be more complex than traditionally appreciated: while mutagenic effects of irradiation should increase the probability of occurrence of oncogenic mutations, IR can also work as a tumor promoter, increasing the selective expansion of clones bearing mutations which become advantageous in the irradiation-altered environment, such as activated mutations in Notch1 or disrupting mutations in p53.
引用
收藏
页码:3005 / 3011
页数:7
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