Holcenberg J S
Cancer Treat Rep. 1979 Jun;63(6):1109-14.
The effect of L-glutamine and L-asparagine depletion by Acinetobacter L-glutaminase-L-asparaginase on the toxicity and antitumor activity of L-(alphaS,5S)-alpha-amino-3-chloro-4,5-dihydro-5-isoxazoleacetic acid (NSC-163501) was tested in mice. The LD50 of six daily doses of NSC-163501 in BDF1 female mice decreased from 7.5 to 0.3 mg/kg/day by combination treatment with the enzyme. Enzyme therapy also decreased the dose of NSC-163501 needed for maximal prolongation of survival in these mice inoculated with L1210 leukemia. Nevertheless, the combination did not prolong survival in L1210-bearing mice beyond that of higher doses of NSC-163501 alone. In contrast, the combination of enzyme plus NSC-163501 inhibited the growth of established sc implanted Ehrlich ascites carcinoma in ICRf male mice much more than either agent alone. Treatment with Acinetobacter L-glutaminase-L-asparaginase decreased the L-asparagine and L-glutamine levels in acid extracts of the Ehrlich tumor. NSC-163501 did not affect the amide levels or alter the decrease produced by enzyme therapy.
研究了不动杆菌L-谷氨酰胺酶-L-天冬酰胺酶消耗L-谷氨酰胺和L-天冬酰胺对L-(αS,5S)-α-氨基-3-氯-4,5-二氢-5-异恶唑乙酸(NSC-163501)毒性和抗肿瘤活性的影响。在BDF1雌性小鼠中,通过酶联合治疗,六日剂量的NSC-163501的半数致死量从7.5降至0.3mg/kg/天。酶疗法还降低了接种L1210白血病的这些小鼠中最大程度延长生存期所需的NSC-163501剂量。然而,联合治疗并未使荷L1210小鼠的生存期超过单独使用高剂量NSC-163501的生存期。相反,酶加NSC-163501的联合治疗对ICRf雄性小鼠中已建立的皮下植入艾氏腹水癌生长的抑制作用比单独使用任何一种药物都要强得多。用不动杆菌L-谷氨酰胺酶-L-天冬酰胺酶治疗可降低艾氏肿瘤酸性提取物中的L-天冬酰胺和L-谷氨酰胺水平。NSC-163501不影响酰胺水平,也不改变酶疗法所产生的降低作用。