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Calcium antagonists as radiation modifiers: site specificity in relation to tumor response.
- Source :
-
International journal of radiation oncology, biology, physics [Int J Radiat Oncol Biol Phys] 1989 May; Vol. 16 (5), pp. 1141-4. - Publication Year :
- 1989
-
Abstract
- The calcium antagonists, verapamil, nifedipine, and flunarizine, were studied for their effects on blood flow and radiation response in SCCVII/St intradermal back tumors, over a dose range of 0.05-50 mg/kg. Verapamil, at low doses, increased tumor blood flow, as measured by relative fluorescence intensity of Ho33342 stain, and increased tumor radiosensitivity. However, at doses of 20 mg/kg and above, verapamil reduced Ho33342 fluorescence intensity, and increased tumor radioresistance. Nifedipine reduced tumor radiosensitivity and Ho33342 fluroscence intensity at doses above 1 mg/kg, but below this dose increased Ho33342 intensity was observed and a small radiosensitization was apparent. Flunarizine sensitized tumors to X rays at all doses tested, although increased Ho33342 intensity was seen only at 5 mg/kg. The relative affinities of these compounds for different sites within the host may explain the variations in blood flow and radiation sensitivity in this tumor system.
- Subjects :
- Animals
Combined Modality Therapy
Female
Flunarizine therapeutic use
Mice
Mice, Inbred C3H
Neoplasm Transplantation
Neoplasms, Experimental blood supply
Neoplasms, Experimental drug therapy
Nifedipine therapeutic use
Verapamil therapeutic use
Calcium Channel Blockers therapeutic use
Neoplasms, Experimental radiotherapy
Radiation-Sensitizing Agents
Subjects
Details
- Language :
- English
- ISSN :
- 0360-3016
- Volume :
- 16
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- International journal of radiation oncology, biology, physics
- Publication Type :
- Academic Journal
- Accession number :
- 2715060
- Full Text :
- https://doi.org/10.1016/0360-3016(89)90269-1