Collery P, Millart H, Pluot M, Anghileri L J
Anticancer Res. 1986 Sep-Oct;6(5):1085-7.
To determine the influence of the length of the treatment on the anatomopathological and biochemical intratumor changes induced by gallium, we treated C3H BA mammary adenocarcinoma-bearing C3H/HeJ mice with gallium chloride daily, for a period of either 21 or 42 days. In both cases the same dose of 200 mg/kg/24h was administered. An increase of collagen fibrosis in treated tumors as opposed to controls was only noted after 42 days, as well as a significant decrease of the intratumor magnesium and calcium concentrations that could be responsible for a reduction in the metabolic activities of the malignant cells. Remarkable intratumor gallium concentrations (38.4 +/- 30.3 nmol/g after 21 days of treatment; 13.4 +/- 7.3 nmol/g after 42 days where the necrosis is much more important) are obtained after this oral administration. There is no renal toxicity and a higher tumor/kidney concentration ratio is obtained than after acute parenteral administration. The effect of gallium may be different according to the mode of administration: it may be more cytotoxic after parenteral administration, while after oral administration it may act as a better metabolic regulator with a more selective tumor uptake and fewer side effects.
为了确定治疗时长对镓诱导的肿瘤组织病理学和生化变化的影响,我们对携带C3H BA乳腺腺癌的C3H/HeJ小鼠每日给予氯化镓治疗,为期21天或42天。两种情况下均给予相同剂量200 mg/kg/24h。仅在42天后才观察到与对照组相比,治疗后肿瘤中的胶原纤维化增加,以及肿瘤内镁和钙浓度显著降低,这可能导致恶性细胞代谢活性降低。经口服给药后,肿瘤内镓浓度显著(治疗21天后为38.4±30.3 nmol/g;42天后为13.4±7.3 nmol/g,此时坏死更为严重)。未出现肾毒性,且与急性非肠道给药后相比,肿瘤/肾脏浓度比更高。镓的作用可能因给药方式而异:非肠道给药后可能具有更强的细胞毒性,而口服给药后可能作为更好的代谢调节剂,具有更高的肿瘤摄取选择性和更少的副作用。