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1
The nitroimidazoles as radiosensitizers and cytotoxic agents.作为放射增敏剂和细胞毒剂的硝基咪唑类药物。
Br J Cancer Suppl. 1978 Jun;3:120-3.
2
Effects of oxygen and misonidazole on cell transformation and cell killing in C3H 10T1/2 cells by X rays in vitro.氧气和米索硝唑对X射线体外诱导C3H 10T1/2细胞转化及细胞杀伤的影响。
Radiat Res. 1984 Oct;100(1):96-103.
3
Some examples of anomalous radiosensitizing behaviour of electron-affinic compounds in vitro.体外亲电子化合物异常放射增敏行为的一些例子。
Br J Cancer Suppl. 1978 Jun;3:80-3.
4
Oncogenic transformations in vitro produced by misonidazole.
Cancer Clin Trials. 1980 Spring;3(1):85-90.
5
Sensitization of ultraviolet radiation damage in bacteria and mammalian cells.细菌和哺乳动物细胞中紫外线辐射损伤的敏化作用。
Br J Cancer Suppl. 1978 Jun;3:111-4.
6
Testing of hypoxic cell radiosensitizers in vivo.体内缺氧细胞放射增敏剂的测试。
Br J Cancer Suppl. 1978 Jun;3:202-5.
7
Misonidazole and MTDQ in combination: cytotoxic and radiosensitizing properties in hypoxic mammalian cells.米索硝唑与MTDQ联合应用:对缺氧哺乳动物细胞的细胞毒性和放射增敏特性
Br J Cancer. 1979 May;39(5):510-5. doi: 10.1038/bjc.1979.94.
8
Oncogenic transformation systems involving mammalian cells in vitro to determine the relative risks of different treatment modalities.
Strahlentherapie. 1984 Dec;160(12):725-31.
9
In vivo evaluation of the radiosensitizing and cytotoxic properties of newly synthesized electron-affinic drugs.新合成的亲电子药物放射增敏和细胞毒性特性的体内评估。
Br J Cancer Suppl. 1978 Jun;3:206-11.
10
Sensitizing and toxicity properties of misonidazole and its derivatives.米索硝唑及其衍生物的致敏性和毒性特性。
Br J Cancer Suppl. 1978 Jun;3:115-9.

引用本文的文献

1
A Multimodal Molecular Imaging Study Evaluates Pharmacological Alteration of the Tumor Microenvironment to Improve Radiation Response.一项多模态分子影像学研究评估了改变肿瘤微环境的药物作用以提高放射反应。
Cancer Res. 2018 Dec 15;78(24):6828-6837. doi: 10.1158/0008-5472.CAN-18-1654. Epub 2018 Oct 9.
2
In vivo interaction of anti-cancer drugs with misonidazole or metronidazole: methotrexate, 5-fluorouracil and adriamycin.抗癌药物与米索硝唑或甲硝唑在体内的相互作用:甲氨蝶呤、5-氟尿嘧啶和阿霉素。
Br J Cancer. 1980 Dec;42(6):861-70. doi: 10.1038/bjc.1980.334.
3
Is tumour radiosensitization by misonidazole a general phenomenon?米索硝唑引起的肿瘤放射增敏是一种普遍现象吗?
Br J Cancer. 1980 Jan;41(1):1-9. doi: 10.1038/bjc.1980.1.
4
Cytotoxicity of metronidazole (Flagyl) and misonidazole (Ro-07-0582): enhancement by lactate.甲硝唑(灭滴灵)和米索硝唑(Ro-07-0582)的细胞毒性:乳酸的增强作用
Br J Cancer. 1981 Mar;43(3):350-4. doi: 10.1038/bjc.1981.55.
5
Factors influencing the chemosensitization of melphalan by misonidazole.米索硝唑影响美法仑化学增敏作用的因素。
Br J Cancer. 1985 Feb;51(2):219-28. doi: 10.1038/bjc.1985.32.

本文引用的文献

1
Split-dose experiments with hypoxic cells. Implications for fractionated and low-dose-rate radiotherapy.
Radiology. 1974 Aug;112(2):425-30. doi: 10.1148/112.2.425.
2
Quantitative and qualitative studies of chemical transformation of cloned C3H mouse embryo cells sensitive to postconfluence inhibition of cell division.对汇合后细胞分裂抑制敏感的克隆C3H小鼠胚胎细胞化学转化的定量和定性研究。
Cancer Res. 1973 Dec;33(12):3239-49.
3
Selective chemotherapy of noncycling cells in an in vitro tumor model.体外肿瘤模型中非循环细胞的选择性化疗。
Cancer Res. 1974 Dec;34(12):3501-3.
4
X-radiation-induced transformation in a C3H mouse embryo-derived cell line.X射线诱导C3H小鼠胚胎来源细胞系发生转化。
Cancer Res. 1976 Apr;36(4):1367-74.
5
Increased cell killing by metronidazole and nitrofurazone of hypoxic compared to aerobic mammalian cells.与需氧哺乳动物细胞相比,甲硝唑和呋喃西林对缺氧哺乳动物细胞的杀伤作用增强。
Cancer Res. 1976 Mar;36(3):930-6.
6
Hypoxic sensitizers: radiobiological studies at the cellular level.缺氧敏化剂:细胞水平的放射生物学研究
Radiology. 1975 Nov;117(2):453-7. doi: 10.1148/117.2.453.
7
Cytotoxicity of Ro-07-0582; enhancement by hyperthermia and protection by cysteamine.Ro-07-0582的细胞毒性;热疗增强作用及半胱胺的保护作用
Br J Cancer. 1977 Jun;35(6):809-15. doi: 10.1038/bjc.1977.122.

作为放射增敏剂和细胞毒剂的硝基咪唑类药物。

The nitroimidazoles as radiosensitizers and cytotoxic agents.

作者信息

Hall E J, Miller R, Astro M, Rini F

出版信息

Br J Cancer Suppl. 1978 Jun;3:120-3.

PMID:277211
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2149404/
Abstract

Using hamster cells in culture, the radiosensitizing and cytotoxic properties of 8 electron-affinic drugs have been compared. These include nitrofurans derivatives as well as 2 and 5-nitroimidazoles. Most work has been performed with misonidazole for which it appears that, at 37 degree C, the concentration of drug required to produce a given level of cell killing is inversely proportional to the square of the exposure time. Misonidazole was also compared with X-rays for its ability to produce neoplastic transformations in vitro, using the C3H 10T 1/2 cell line.

摘要

利用培养的仓鼠细胞,比较了8种亲电子药物的放射增敏和细胞毒性特性。这些药物包括硝基呋喃衍生物以及2-硝基咪唑和5-硝基咪唑。大多数研究是针对米索硝唑进行的,在37℃时,产生给定细胞杀伤水平所需的药物浓度似乎与照射时间的平方成反比。还使用C3H 10T 1/2细胞系,比较了米索硝唑与X射线在体外诱导肿瘤转化的能力。