There is increasing concern for the oncogenic potential of agents used to treat cancer. To some extent, concern about the production of a second malignancy is the price of success. After all, the patient must be a long-term survivor, with the first malignancy cured--or at least controlled--before the possibility of a treatment-induced second malignancy becomes a problem. Hyperthermia is one of the few modalities used to treat cancer which does not of itself induce oncogenic transformations; by comparison, radiation is a weak oncogenic agent, while some chemotherapy agents are relatively potent. The purpose of the present application is to explore pragmatic and mechanistic aspects of the interaction of heat, chemotherapy agents, and radiation as they relate to oncogenic transformation.
The first aims i s to determine whether hyperthermia, used to potentiate chemotherapy agents, enhances the transformation incidence to the same extent as it enhances cell lethality. To be specific, for a given level of cell killing, does not thermochemotherapy produce an equally elevated level of oncogenic transformation, or can a sequence be found where cytotoxicity is enhanced without a concomitant increase in oncogenicity? This has proved to be the case for X rays and for the chemotherapy agents investigated to date, namely actinomycin-D, BCNU and mitomycin-C. The range of chemotherapy agents tested in combination with heat will be extended to include bleomycin, melphalan, and cis-platinum, and oncogenic transformation will be monitored in vitro using C3H 10T1/2 cells. Attention will focus also on the transient phenomenon of thermotolerance, whereby cells exposed to an initial heat treatment develop resistance to killing by subsequent heat exposures. We will determine whether or not thermotolerant cells are also resistant to the induction of transformation by X rays and chemotherapeutic agents. The development of thermotolerance will be monitored by the appearance of """"""""heat-shock"""""""" proteins and checked by enhanced cell survival.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
2R01CA043194-04A1
Application #
3185204
Study Section
Radiation Study Section (RAD)
Project Start
1986-08-01
Project End
1994-11-30
Budget Start
1989-12-01
Budget End
1990-11-30
Support Year
4
Fiscal Year
1990
Total Cost
Indirect Cost
Name
Columbia University (N.Y.)
Department
Type
Schools of Medicine
DUNS #
064931884
City
New York
State
NY
Country
United States
Zip Code
10027
Miller, R C; Richards, M; Baird, C et al. (1994) Interaction of hyperthermia and chemotherapy agents;cell lethality and oncogenic potential. Int J Hyperthermia 10:89-99
Roizin-Towle, L; Yarlett, N; Pirro, J P et al. (1990) Hyperthermia studies in polyamine-altered human lung carcinoma cells. Radiat Res 124:S80-7
Miller, R C; Roizin-Towle, L; Komatsu, K et al. (1989) Interaction of heat with X-rays and cis-platinum;cell lethality and oncogenic transformation. Int J Hyperthermia 5:697-705
Hall, E J; Hei, T K; Miller, R C (1989) Modulation of the oncogenic potential of various anticancer modalities. Front Radiat Ther Oncol 23:131-9 discussion 160-1
Komatsu, K; Miller, R C; Hall, E J (1988) The oncogenic potential of a combination of hyperthermia and chemotherapy agents. Br J Cancer 57:59-63