In the interest of improving cancer treatment, considerable attention has been placed on the modification of radiation damage. The interaction of a variety of chemotherapy and/or molecularly targeted agents with radiation is under study to determine if tumors can be made more sensitive or normal tissues more resistant to radiation treatment. The central aim is to identify approaches that will result in a net therapeutic gain, thus improving cancer treatment with radiation. One goal of the project is to define and better understand those aspects of tumor physiology, including cellular and molecular processes and the influence of the tumor microenvironment on treatment response. The ability to enhance the response of the tumor to radiation, without enhancing normal tissue within a given treatment field is desirable. A CK2 inhibitor was evaluated as a radiation sensitizer in human tumor cell lines and found to be quite effective;however, the enhancement in radiosensitivity was not observed in a xenograft model. Currently, a PI3K/mTOR inhibitor is being evaluated in human head/neck carcinoma cells lines. Impressive radiosensitization by the inhibitor is observed in vitro and xenograft studies are underway. We are currently evaluating a number of metabolic inhibitors as radiation modifiers under the working hypothesis that inhibition of metabolism (for example, decreased ATP production) will diminish the repair of radiation-induced DNA damage. A Glut1 inhibitor has been identified as a significant radiation modifier and studies are ongoing as to the mechanism of action and whether that agent will enhance the radiosensitivity of xenografts. With respect to normal tissue response to radiation, we found rapamycin protects against radiation-induced oral mucositis in part by preventing radiation induced stem cell senescence. It was also demonstrated that mice that express a Smad7 transgene were resistant to radiation-induced mucositis by repressing activation of the TGF-beta signaling pathway. Topical application of Smad7 protein conjugated with cell-permeable Tat tag showed prophylatic and therapeutic effects on radiation-induced oral mucositis in mice. Oral mucositis is a common toxicity associated with the chemoradiation (cisplatin combined with fractionated radiation) treatment of head and neck cancers. Tempol also protects against chemoradiation-induced mucositis yet does not alter chemoradiation with respect to tumor regrowth delay. Collectively we have identified a number of pre-clinical approaches to initiate human radiation oncology clinical trials for protection against radiation-induced mucositis.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Investigator-Initiated Intramural Research Projects (ZIA)
Project #
1ZIASC006321-34
Application #
8763674
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
34
Fiscal Year
2013
Total Cost
$559,816
Indirect Cost
Name
National Cancer Institute Division of Clinical Sciences
Department
Type
DUNS #
City
State
Country
Zip Code
Kesarwala, Ah; Krishna, Mc; Mitchell, Jb (2014) Oxidative stress in oral diseases. Oral Dis :
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Friedman, Jay A; Wise, Stephanie C; Hu, Michael et al. (2013) HSP90 Inhibitor SNX5422/2112 Targets the Dysregulated Signal and Transcription Factor Network and Malignant Phenotype of Head and Neck Squamous Cell Carcinoma. Transl Oncol 6:429-41
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Palayoor, Sanjeewani T; Mitchell, James B; Cerna, David et al. (2008) PX-478, an inhibitor of hypoxia-inducible factor-1alpha, enhances radiosensitivity of prostate carcinoma cells. Int J Cancer 123:2430-7

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