Rosenblum M G
Department of Clinical Immunology and Biological Therapy, University of Texas System, M.D. Anderson Cancer Center, Houston 77030.
Lymphokine Cytokine Res. 1991 Apr;10(1-2):83-7.
DFMO and IFN have both been shown to suppress the intracellular activity of ornithine decarboxylase in rapidly proliferating tissues. In addition, both agents demonstrate antiproliferative activity against human lymphoblastoid (Daudi) cells in culture. Treatment of log-phase Daudi cells with doses of 6 U/ml of IFN or 1 mM DFMO resulted in a 50% reduction of cell number 72 h after drug addition. Combination of IFN with DFMO against DAUDI cells using the isobologram method showed that the two demonstrate true antiproliferative synergy. Analysis of 2',5'-oligoadenylate synthetase (2,5A) activity in treated cells showed that both IFN alone and IFN/DFMO combination result in equivalent 2,5A induction (1800 mmol/mg/20 h) compared to control (300 mmol/mg/20 h). While 2,5A activity decreased by 50% at 48 h in cells after treatment with IFN alone, the IFN/DFMO combination remained elevated (1700 mmol/mg/20 h). Phosphodiesterase (PdE) activity in these cells showed no substantial changes with IFN, DFMO, or IFN/DFMO treatment over 72 h compared to control values. In contrast, the activity of the 68-kDa interferon induced protein kinase (PK) in IFN/DFMO-treated cells was 1.6-fold greater at 48 and 72 h than that found for IFN alone. These studies demonstrate that the synergistic antiproliferative activity of IFN/DFMO combination may be due, in part, to modification of the activity of IFN-inducible enzymes.
DFMO和IFN均已被证明可抑制快速增殖组织中鸟氨酸脱羧酶的细胞内活性。此外,这两种药物在培养中均对人淋巴母细胞样(Daudi)细胞表现出抗增殖活性。用6 U/ml的IFN或1 mM DFMO处理对数期Daudi细胞,在添加药物72小时后细胞数量减少了50%。使用等效线图法将IFN与DFMO联合用于处理DAUDI细胞,结果表明二者表现出真正的抗增殖协同作用。对处理后细胞中的2',5'-寡腺苷酸合成酶(2,5A)活性进行分析,结果显示与对照(300 mmol/mg/20小时)相比,单独使用IFN以及IFN/DFMO联合使用均导致等效的2,5A诱导(1800 mmol/mg/20小时)。虽然单独用IFN处理后的细胞在48小时时2,5A活性降低了50%,但IFN/DFMO联合处理后的细胞中该活性仍保持升高(1700 mmol/mg/20小时)。与对照值相比,在72小时内,这些细胞中的磷酸二酯酶(PdE)活性在用IFN、DFMO或IFN/DFMO处理后没有实质性变化。相反,在48小时和72小时时,IFN/DFMO处理的细胞中68 kDa干扰素诱导蛋白激酶(PK)的活性比单独使用IFN时高1.6倍。这些研究表明,IFN/DFMO联合使用的协同抗增殖活性可能部分归因于对IFN诱导酶活性的改变。