Division of Cancer Pathobiology, Department of Pathology and Laboratory Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104, USA; The Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
University Paris Diderot, Sorbonne Paris Cité, Epigenetics and Cell Fate, UMR 7216 CNRS, 75013 Paris, France.
Cell Host Microbe. 2014 Mar 12;15(3):283-94. doi: 10.1016/j.chom.2014.02.010.
Maintaining genome integrity and transmission of intact genomes is critical for cellular, organismal, and species survival. Cells can detect damaged DNA, activate checkpoints, and either enable DNA repair or trigger apoptosis to eliminate the damaged cell. Aberrations in these mechanisms lead to somatic mutations and genetic instability, which are hallmarks of cancer. Considering the long history of host-microbe coevolution, an impact of microbial infection on host genome integrity is not unexpected, and emerging links between microbial infections and oncogenesis further reinforce this idea. In this review, we compare strategies employed by viruses, bacteria, and parasites to alter, subvert, or otherwise manipulate host DNA damage and repair pathways. We highlight how microbes contribute to tumorigenesis by directly inducing DNA damage, inactivating checkpoint controls, or manipulating repair processes. We also discuss indirect effects resulting from inflammatory responses, changes in cellular metabolism, nuclear architecture, and epigenome integrity, and the associated evolutionary tradeoffs.
维持基因组完整性和完整基因组的传递对于细胞、生物和物种的生存至关重要。细胞可以检测到受损的 DNA,激活检查点,并使 DNA 修复或触发细胞凋亡以消除受损细胞。这些机制的异常会导致体细胞突变和遗传不稳定性,这是癌症的标志。考虑到宿主-微生物共同进化的悠久历史,微生物感染对宿主基因组完整性的影响并不出人意料,而微生物感染与肿瘤发生之间新出现的联系进一步强化了这一观点。在这篇综述中,我们比较了病毒、细菌和寄生虫用来改变、颠覆或操纵宿主 DNA 损伤和修复途径的策略。我们强调了微生物如何通过直接诱导 DNA 损伤、失活检查点控制或操纵修复过程来促进肿瘤发生。我们还讨论了炎症反应、细胞代谢、核结构和表观基因组完整性的变化以及相关的进化权衡所带来的间接影响。