Cancer radiotherapy by combined use of radioprotectors and a radiosensitizer (in Japanese)
Subcutaneous or intraperitoneal administration of 1-cysteine, 1-cysteine- d-glucose, MEA, or AET raised the survivals of male mice and decreased a loss of body weight from single or fractionated x irradiation. Among the SH compounds, AET is the most effective, and MEA is the next. In rats bearing Yoshida sarcoma, 5-flourouracil (5FU) was found to be effective as a radiosensitizer in radiation- induced depression of mitotic index of Yoshida sarcoma. Administration of MEA or 1-cysteine failed to alter the reduction of mitotic index of the sarcoma cells in rats treated with 5FU and x rays. This suggests that two SH compounds did not protect tumor cells from combined effects of 5FU and x rays. If the SH compounds exerted protective effects on normal tissues of rats, the effective killing of tumors may result in prolongation of survival times of rats bearing Yoshida sarcoma. However, the present experiments showed that the SH compounds did not prolong the survival time of the tumor-bearing rats. (auth)
- Research Organization:
- Tokyo Teishin Hospital
- NSA Number:
- NSA-29-000726
- OSTI ID:
- 4420217
- Journal Information:
- Nippon Igaku Hoshasen Gakkai Zasshi, v. 33, no. 4, pp. 351-359, Journal Name: Nippon Igaku Hoshasen Gakkai Zasshi, v. 33, no. 4, pp. 351-359; ISSN NHGZA
- Country of Publication:
- Japan
- Language:
- Japanese
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