Carr Laurie L, Gottschling Daniel E
Division of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
Exp Gerontol. 2008 Mar;43(3):123-9. doi: 10.1016/j.exger.2007.10.010. Epub 2007 Nov 28.
The striking correlation between advanced age and an increased incidence of cancer has led investigators to examine the influence of aging on genome maintenance. Because loss of heterozygosity (LOH) can lead to the inactivation of tumor suppressor genes, and thus carcinogenesis, understanding the affect of aging on this type of mutation event is particularly important. Several factors may affect the rate of LOH, including an increase in the amount of DNA damage, specifically double-strand breaks (DSBs), and the ability to efficiently repair this damage via pathways that minimize the loss of genetic information. Because of experimental constraints, there is only suggestive evidence for a change in the rate of DNA damage as humans age. However, recent studies in model organisms find that there are increased rates of LOH with age, and that repair of DNA damage occurs via a different pathway in old cells versus young cells. We speculate that the age-dependent change in DNA repair may explain why there is increased LOH, and that the findings from these model organisms may extend to humans.
高龄与癌症发病率增加之间显著的相关性促使研究人员去研究衰老对基因组维持的影响。由于杂合性缺失(LOH)会导致肿瘤抑制基因失活,进而引发癌症,因此了解衰老对这类突变事件的影响尤为重要。有几个因素可能会影响LOH的发生率,包括DNA损伤量的增加,特别是双链断裂(DSB),以及通过尽量减少遗传信息丢失的途径有效修复这种损伤的能力。由于实验限制,关于随着人类年龄增长DNA损伤率变化的证据仅有提示性。然而,最近在模式生物中的研究发现,随着年龄增长LOH发生率增加,并且与年轻细胞相比,老细胞中DNA损伤的修复途径不同。我们推测,DNA修复中与年龄相关的变化可能解释了为什么LOH会增加,并且这些模式生物的研究结果可能适用于人类。