Our group is currently focusing on three aspects of H2AX. The first includes translational projects aimed at making H2AX phosphorylation a useful biodosimeter in humans and other animals.
The aim of this aspect is to provide a mechanism by which physicians can get biological feedback from individual patients on the efficiency of a treatment in order to modify and optimize that treatment. The second utilizes the finding that H2AX phosphorylation is several orders of magnitude more sensitive than previous methods of DSB detection, making it a uniquely useful means of uncovering novel roles for DSBs in cellular metabolism. The third involves gaining insight into focal structure and mechanism of growth. The first aspect includes projects involving not only biodosimetry of ionizing radiation, which directly causes DSBs in cellular DNA, but also of various drugs that indirectly cause DSBs by interfering with cellular metabolism. We are in the process of determining the limits of DSB detection after whole body exposure of animals to ionizing radiation using H2AX phosphorylation as a model for triage during a radiation-related emergency. The results show that the amount of exposure to ionizing radiation in the sublethal to lethal range can be measured up to four days post exposure. We are also investigating the usefulness of gamma-H2AX detection in cases of partial body exposure. Concerning chemotherapeutic agents, two recent developments have given considerable impetus to this project. The first development is the finding by us and others that gamma-H2AX is formed in tissue culture cells as a response not only to agents that directly cause DSBs but also to those that indirectly induce DSBs. As many of the agents used for cancer treatment fall into this latter category, this finding greatly increases possible roles for gamma-H2AX as a biomarker for drug responses. The second important development is the formation of a multi-disiplinary NCI team to expedite the clinical evaluation of new therapeutic and imaging agents, so-called phase zero trials. gamma-H2AX formation is being examined as a possible biodosimeter in these studies utilizing several possible surrogate tissues. We are also examining gamma-H2AX formation in mouse models and are involved in several clinical protocols either approved or being approved in the phase zero and phase one trials. This work is important because it will permit clinicians to obtain immediate feedback from the cells of an individual patient, feedback which can then be used to tailor the treatment to that patient, thereby improving their survival. The ultimate goal of this initiative is to develop gamma-H2AX detection into a useful tool for human health. The second aspect involves the use of gamma-H2AX to probe for interactions between cells in animals. In vitro studies by us and others have shown that cells that have been exposed to ionizing radiation lead to the presence of DNA damage products in unexposed cells that contact the exposed cells or media from the exposed cells and affect their viability, a phenomenon known as the bystander effect. We have shown that a robust bystander effect is present in artificial human skin tissue. Working from the hypothesis that the bystander effect is an example of a larger phenomenon of communication among damaged and healthy cells, we have demonstrated that media from tumor cells induces responses in bystander cells indistinguishable from those induced by media from irradiated cells, and are currently demonstrating the ability of other stresses to induce bystander responses. In addition, we are finding that this communication can be demonstrated in the intact animal. The presence of a human tumors implanted into syngeneic mice leads to higher levels of DNA damage in certain other cells in the mouse. We have determined that macrophages are involved in this communication and proliferating tissues are most sensitive. We are continuing to investigate when and how this communication takes place in the animal and how this might be useful for human health. This work is important because it may increase the ways information can be obtained from individual patients. It is possible that by monitoring certain easily obtained tissues of a patient, information can be obtained about events in other less accessible tissues, perhaps leading to early detection of disease and/or optimization of treatment. The third aspect focuses on the structure and dynamism of the gamma-H2AX focus. We are developing tools that will permit us to study focal substructure and how it changes with time. We have shown for example, that in yeast, Mre11 does not bind to the whole gamma-H2AX domain, but is concentrated next to the break site. Studies such as these will complement other findings concerning the interactions of various proteins with gamma-H2AX, leading to a greater understanding of DNA DSB repair and the maintenance of genome stability. This work is important as iot will provide the basis for understanding the important parameters involved in utilizing gamma-H2AX foci as a biodosimeter.
| Lobachevsky, Pavel; Leong, Trevor; Daly, Patricia et al. (2016) Compromized DNA repair as a basis for identification of cancer radiotherapy patients with extreme radiosensitivity. Cancer Lett 383:212-219 |
| Moroni, Maria; Maeda, Daisuke; Whitnall, Mark H et al. (2013) Evaluation of the gamma-H2AX assay for radiation biodosimetry in a swine model. Int J Mol Sci 14:14119-35 |
| Dickey, Jennifer S; Gonzalez, Yanira; Aryal, Baikuntha et al. (2013) Mito-tempol and dexrazoxane exhibit cardioprotective and chemotherapeutic effects through specific protein oxidation and autophagy in a syngeneic breast tumor preclinical model. PLoS One 8:e70575 |
| Weyemi, Urbain; Redon, Christophe E; Parekh, Palak R et al. (2013) NADPH Oxidases NOXs and DUOXs as putative targets for cancer therapy. Anticancer Agents Med Chem 13:502-14 |
| Ivashkevich, Alesia; Redon, Christophe E; Nakamura, Asako J et al. (2012) Use of the ?-H2AX assay to monitor DNA damage and repair in translational cancer research. Cancer Lett 327:123-33 |
| Dickey, Jennifer S; Baird, Brandon J; Redon, Christophe E et al. (2012) Susceptibility to bystander DNA damage is influenced by replication and transcriptional activity. Nucleic Acids Res 40:10274-86 |
| Weyemi, Urbain; Parekh, Palak R; Redon, Christophe E et al. (2012) SOD2 deficiency promotes aging phenotypes in mouse skin. Aging (Albany NY) 4:116-8 |
| Redon, Christophe E; Weyemi, Urbain; Parekh, Palak R et al. (2012) ?-H2AX and other histone post-translational modifications in the clinic. Biochim Biophys Acta 1819:743-56 |
| Adams, Gerard; Martin, Olga A; Roos, Daniel E et al. (2012) Enhanced intrinsic radiosensitivity after treatment with stereotactic radiosurgery for an acoustic neuroma. Radiother Oncol : |
| Martin, Olga A; Redon, Christophe E; Dickey, Jennifer S et al. (2011) Para-inflammation mediates systemic DNA damage in response to tumor growth. Commun Integr Biol 4:78-81 |
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