Kent C R, Blekkenhorst G H
Department of Radiotherapy, Groote Schuur Hospital/University of Cape Town, South Africa.
Radiat Res. 1988 Dec;116(3):539-46.
Diethyldithiocarbamate (DDC) has been suggested to have both radiosensitizing (due to superoxide dismutase (SOD) inhibition) and radioprotective properties. We have studied the activity of SOD up to 24 h after intratumoral administration of 50, 100, 150, and 300 mg/kg DDC in 3-methylcholanthrene-induced tumors in BALB/c mice. Maximal inhibition of SOD (8% of control) was obtained 1 h after administration of 100 mg/kg DDC. Tumor response to DDC and X irradiation was assessed using a tumor growth-delay assay, after 11 Gy 100-kVp X rays given up to 24 h after DDC administration. Radiation-induced tumor growth delay (7.11 +/- 1.76 days) was enhanced only when tumors were irradiated 2-4 h after 50 mg/kg DDC. When higher doses of DDC were used, tumor cure was noted when DDC was injected 1-6 h before irradiation. We suggest our findings are consistent with radiosensitization being due to SOD inhibition, but that if insufficient time is allowed between DDC injection and irradiation, the sensitization is masked by a radioprotective effect. We believe that further investigations as to the therapeutic potential of DDC in human patients with cancer are warranted.
二乙基二硫代氨基甲酸盐(DDC)被认为具有放射增敏作用(由于抑制超氧化物歧化酶(SOD))和辐射防护特性。我们研究了在BALB/c小鼠中,经3-甲基胆蒽诱导产生肿瘤后,瘤内注射50、100、150和300mg/kg DDC后长达24小时内SOD的活性。注射100mg/kg DDC后1小时,SOD受到最大抑制(为对照组的8%)。在DDC给药后长达24小时内给予11Gy 100-kVp X射线后,使用肿瘤生长延迟试验评估肿瘤对DDC和X射线的反应。仅当在50mg/kg DDC给药后2-4小时照射肿瘤时,辐射诱导的肿瘤生长延迟(7.11±1.76天)才会增强。当使用更高剂量的DDC时,在照射前1-6小时注射DDC会出现肿瘤治愈的情况。我们认为我们的研究结果与放射增敏作用是由于SOD抑制一致,但如果在DDC注射和照射之间没有足够的时间间隔,这种增敏作用会被辐射防护效应掩盖。我们认为有必要进一步研究DDC在人类癌症患者中的治疗潜力。