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Ayako Nakamura-Ishizu
Department School of Medicine, School of Medicine Position Professor and Division head |
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| Article types | Original article |
| Language | English |
| Peer review | Peer reviewed |
| Title | Pathological neoangiogenesis depends on oxidative stress regulation by ATM. |
| Journal | Formal name：Nature medicine Abbreviation：Nat Med ISSN code：1546170X/10788956 |
| Domestic / Foregin | Foregin |
| Volume, Issue, Page | 18(8),pp.1208-16 |
| Author and coauthor | Okuno Yuji, Nakamura-Ishizu Ayako, Otsu Kinya, Suda Toshio, Kubota Yoshiaki |
| Publication date | 2012/08 |
| Summary | The ataxia telangiectasia mutated (ATM) kinase, a master regulator of the DNA damage response (DDR), acts as a barrier to cellular senescence and tumorigenesis. Aside from DDR signaling, ATM also functions in oxidative defense. Here we show that Atm in mice is activated specifically in immature vessels in response to the accumulation of reactive oxygen species (ROS). Global or endothelial-specific Atm deficiency in mice blocked pathological neoangiogenesis in the retina. This block resulted from increased amounts of ROS and excessive activation of the mitogen activated kinase p38α rather than from defects in the canonical DDR pathway. Atm deficiency also lowered tumor angiogenesis and enhanced the antiangiogenic action of vascular endothelial growth factor (Vegf) blockade. These data suggest that pathological neoangiogenesis requires ATM-mediated oxidative defense and that agents that promote excessive ROS generation may have beneficial effects in the treatment of neovascular disease. |
| DOI | 10.1038/nm.2846 |
| PMID | 22797809 |