The inability of radiotherapy to control tumor growth is still a daunting clinical problem leading to failure of the overall treatment regimens. The fundamental question is; could tumor cells be specifically sensitized to ionizing radiations (IR) by heat or agents that produce effects similar to heat by targeting essential molecules or structures exclusively expressed (present) in tumor cells. One such factor, expressed in most tumors and silent in somatic cells, is telomerase, the enzyme required for cell immortality. Because of this, telomerase is an attractive target for inhibition in anticancer therapy. Telomeres are maintained by telomerase and the catalytic unit of telomerase (TERT) interacts with HSP70. Telomere stability is influenced by ATM (ataxia telangiectasia mutated), a major regulator of cellular responses to IR. ATM, a protein kinase, is activated by IR and phosphorylates a number of different substrates following activation. TERT activity is negatively regulated by downstream effectors of ATM. Based on the fact that hTERT interacts with HSP70 and such interactions may be dependent on ATM signaling, thereby potentially altering the tumor cells' response to IR. To test our hypothesis that heat treatment modulates the IR induced ATM and TERT signaling pathway, experiments will be performed to determine whether heat treatment influences radiation induced ATM kinase activity, telomerase activity, telomere structure and TERT interactions with telomeres in cells with and without expression of HSP70 and/or HSC70. In addition, experiments are proposed that will elucidate whether inactivation of ATM and TERT function will enhance the heat induced sensitization to IR induced cell kill. Determining the influence of heat and/or IR on ATM function and telomere metabolism in presence and absence of HSP70 and/or HSC70 will not only add to our understanding of the mechanisms of heat induced radiosensitization but may also aid the development of new tumor treatment strategies.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
5P01CA104457-04
Application #
7475633
Study Section
Subcommittee G - Education (NCI)
Project Start
Project End
Budget Start
2007-07-01
Budget End
2008-06-30
Support Year
4
Fiscal Year
2007
Total Cost
$255,957
Indirect Cost
Name
Washington University
Department
Type
DUNS #
068552207
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Wang, Rongsheng E; Pandita, Raj K; Cai, Jianfeng et al. (2012) Inhibition of heat shock transcription factor binding by a linear polyamide binding in an unusual 1:1 mode. Chembiochem 13:97-104
Wang, Rongsheng E; Hunt, Clayton R; Chen, Jiawei et al. (2011) Biotinylated quercetin as an intrinsic photoaffinity proteomics probe for the identification of quercetin target proteins. Bioorg Med Chem 19:4710-20
Thirupathi Reddy, Y; Narsimha Reddy, P; Koduru, Srinivas et al. (2010) Aplysinopsin analogs: Synthesis and anti-proliferative activity of substituted (Z)-5-(N-benzylindol-3-ylmethylene)imidazolidine-2,4-diones. Bioorg Med Chem 18:3570-4
Reddy, Y Thirupathi; Sekhar, Konjeti R; Sasi, Nidhish et al. (2010) Novel substituted (Z)-5-((N-benzyl-1H-indol-3-yl)methylene)imidazolidine-2,4-diones and 5-((N-benzyl-1H-indol-3-yl)methylene)pyrimidine-2,4,6(1H,3H,5H)-triones as potent radio-sensitizing agents. Bioorg Med Chem Lett 20:600-2
Pruitt, Rory; Sasi, Nidhish; Freeman, Michael L et al. (2010) Radiosensitization of cancer cells by hydroxychalcones. Bioorg Med Chem Lett 20:5997-6000
Penthala, Narsimha Reddy; Yerramreddy, Thirupathi Reddy; Crooks, Peter A (2010) Microwave assisted synthesis and in vitro cytotoxicities of substituted (Z)-2-amino-5-(1-benzyl-1H-indol-3-yl)methylene-1-methyl-1H-imidazol-4(5H)-ones against human tumor cell lines. Bioorg Med Chem Lett 20:591-3
Geng, Ling; Rachakonda, Girish; Morré, D James et al. (2009) Indolyl-quinuclidinols inhibit ENOX activity and endothelial cell morphogenesis while enhancing radiation-mediated control of tumor vasculature. FASEB J 23:2986-95
Zeng, Sicong; Xiang, Tao; Pandita, Tej K et al. (2009) Telomere recombination requires the MUS81 endonuclease. Nat Cell Biol 11:616-23
Wang, Rongsheng E; Kao, Jeffrey L-F; Hilliard, Carolyn A et al. (2009) Inhibition of heat shock induction of heat shock protein 70 and enhancement of heat shock protein 27 phosphorylation by quercetin derivatives. J Med Chem 52:1912-21
Vanderwaal, Robert P; Maggi Jr, Leonard B; Weber, Jason D et al. (2009) Nucleophosmin redistribution following heat shock: a role in heat-induced radiosensitization. Cancer Res 69:6454-62

Showing the most recent 10 out of 29 publications