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In vivo cell cycle phase-preferential killing of murine fibrosarcoma cells by cisplatin.

Fibrosarcoma cells were separated by centrifugal elutriation. Selected populations enriched in G1-, S-, or G2 + M-phase cells were then injected (10(4) cells) into the tail veins of C3Hf/Kam mice. Twenty minutes after, 4 mg/kg of cisplatin was injected iv into one half of the animals in each experimental group. Fourteen days later the number of lung colonies was scored, and the surviving fractions were plotted against the elutriator fraction numbers. The results indicated that all phases of the cell cycle were sensitive to cisplatin but that the G1 phase was the most sensitive by a factor of ten. Biphasic dose-response curves were observed for unseparated control, S-phase, and G2 + M-phase tumor cell populations, indicating a resistant cell population. G1 cells, however, had long killing over four decades without the resistant tail. Using this in vivo system, it is concluded that cisplatin kills cells throughout the cell cycle but exhibits preferential killing of G1 tumor cells.

Animals↗

Lysozyme enhancement of tumor cell immunoprotection in a murine fibrosarcoma.

We examined the ability of human lysozyme (HLZM) to enhance the immunogenicity of a methylcholanthrene-induced murine fibrosarcoma of C57BL/10 mice. Following s.c. injection of 10(4) live tumor cells, 100% of mice developed palpable tumors within 16 +/- 3 (S.D.) days. Prechallenge immunization with 10(6) irradiated tumor cells with or without complete Freund's adjuvant resulted in protection from tumor development in 14 and 22% of mice, respectively. Incubation of tumor cells with HLZM prior to immunization approximately doubled the degree of protection, with 42 to 44% of mice remaining free of tumor. This enhanced protection was dependent on the enzymatic activity of HLZM. These data suggest that HLZM enhances tumor cell immunogenicity in this model.

Adjuvants, Immunologic↗