米索硝唑对小鼠可移植移行细胞膀胱癌放射敏感性的影响。

Investigative urology Pub Date : 1981-07-01
N Hampel, L Persky
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引用次数: 0

摘要

米索硝唑(Ro-07-0582)的放射增敏性能NSC-26137在N-[4-(5-硝基-2-呋喃基)-2-噻唑基]甲酰胺(FANFT)诱导的C3H/He小鼠移行细胞膀胱癌的腿部移植模型中的作用。荷瘤动物接受400拉德X 5或600拉德X 5的分次辐射。其他放射剂量相同的组在每次放射前给予米索硝唑(0.75 mg / g)治疗。单独放疗可有效延长平均生存时间,400拉德× 5为17%,600拉德× 5为45%,并可延缓肿瘤生长。米索硝唑在600拉德X 5组中显示出放射增敏效应,通过进一步减缓肿瘤生长和延长平均生存时间比对照组延长80%,比单独放疗延长24%。米索硝唑单用无明显细胞毒作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Influence of misonidazole on the radiosensitivity of transplantable transitional cell bladder carcinoma in mice.

The radiosensitizing properties of misonidazole (Ro-07-0582; NSC-26137) were evaluated in a leg transplanted model of N-[4-(5-nitro-2-furyl)-2-thiazolyl]formamide (FANFT) induced transitional cell bladder carcinoma in C3H/He mice. Animals bearing tumor received fractionated radiation of 400 rads X 5 or 600 rads X 5. Other groups with the same radiation doses were treated with misonidazole (0.75 mg per g) before each radiation fraction. Radiation alone was effective in prolonging Mean Survival Time, 17 per cent for 400 rads X 5 and 45 per cent for 600 X 5, with an associated delay in tumor growth. Misonidazole in the 600 rads X 5 group showed a radiosensitizing effect by further slowing tumor growth and prolonging Mean Survival Time by 80 per cent over the control and 24 per cent over radiation alone. Misonidazole alone did not show notable cytotoxic effects.

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