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双功能放射增敏剂KIN-806与其类似物KIN-804和KIN-844相比的免疫增强作用。

The immunopotentiation effects of the bifunctional radiosensitizer KIN-806 in comparison with its analogs KIN-804 and KIN-844.

作者信息

Inomata T, Ogawa Y, Nishioka A, Hamada N, Ito S, Kariya S, Yoshida S, Nagasawa H, Hori H, Inayama S

机构信息

Department of Radiology, Kochi Medical School, Kohasu, Oko-cho, Nankoku-city, Kochi 783-8505, Japan.

出版信息

Oncol Rep. 1999 Nov-Dec;6(6):1209-12. doi: 10.3892/or.6.6.1209.

Abstract

KIN-806 is one of the 2-nitroimidazole derivative hypoxic cell radiosensitizers. Its radiosensitizing effects and the degree of lung metastasis detected were evaluated and compared with its analogs KIN-804 and KIN-844. The immune reactions induced by these radiosensitizers were also analyzed. Female C3H/He mice and SCCVII tumor cells were used. Seventeen days after inoculation of SCCVII tumor cells into the animals, 0.4 g/kg of KIN-806, KIN-804, and KIN-844 was administered to each radiosensitizer group 30 min before 40 Gy was delivered as local irradiation. In each group, KIN-806, KIN-804, and KIN-844 markedly suppressed tumor regrowth in comparison with animals that received irradiation alone. There was no significant difference in the radiosensitizing effects among these three radiosensitizers. A marked suppression of lung metastasis and macrophage/T-lymphocyte infiltration into the tumor were observed only in the KIN-806-administered groups, regardless of the presence or absence of radiation therapy. It therefore appears likely that the lung metastasis suppression was caused by the immune reaction elicited by KIN-806, which is an excellent immunopotentiator as well as an effective radiosensitizer.

摘要

KIN - 806是2 - 硝基咪唑衍生物类乏氧细胞放射增敏剂之一。评估了其放射增敏效果以及检测到的肺转移程度,并与其类似物KIN - 804和KIN - 844进行比较。还分析了这些放射增敏剂诱导的免疫反应。使用雌性C3H/He小鼠和SCCVII肿瘤细胞。在给动物接种SCCVII肿瘤细胞17天后,在进行40 Gy局部照射前30分钟,给每个放射增敏剂组施用0.4 g/kg的KIN - 806、KIN - 804和KIN - 844。与仅接受照射的动物相比,每组中的KIN - 806、KIN - 804和KIN - 844均显著抑制了肿瘤再生长。这三种放射增敏剂的放射增敏效果没有显著差异。仅在施用KIN - 806的组中观察到肺转移和巨噬细胞/T淋巴细胞浸润到肿瘤中的显著抑制,无论是否进行放射治疗。因此,肺转移抑制似乎是由KIN - 806引发的免疫反应所致,KIN - 806既是一种出色的免疫增强剂,也是一种有效的放射增敏剂。

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