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Journal ArticleDOI

Cytotoxic effects of the hypoxic cell radiosensitizer Ro 7-0582 to tumor cells in vivo.

J. Martin Brown
- 01 Dec 1977 - 
- Vol. 72, Iss: 3, pp 469-486
TLDR
The cytotoxicity of the nitroimidazole Ro 7-0582 to tumor cells has been studied in vivo using two transplantable tumors, the EMT6 tumor in BALB/c mice and the MDAH/MCa4 tumor in C3H mice.
Abstract
The cytotoxicity of the nitroimidazole Ro 7-0582 to tumor cells has been studied in vivo using two transplantable tumors, the EMT6 tumor in BALB/c mice and the MDAH/MCa4 tumor in C3H mice. It was found that a high dose of Ro 7-0582 (1 mg/g) was toxic to approximately 90% of the tumor cells, that the toxicity only occurred when the tumor contained hypoxic cells, and that the toxicity was directed at both hypoxic and well-oxygenated cells. Also, there was little or no selective toxicity to irradiated, as opposed to unirradiated, tumor cells. The relative contributions of cytotoxicity and radiosensitization were evaluated in a tumor cure experiment for the MDAH/MCa4 tumor in C3H mice injected with 1 mg/g of Ro 7-0582. Calculations showed that in the absence of cytotoxicity the dose modification factor due to radiosensitization alone would have been 2.02 rather than the value of 2.30 observed. No toxicity was observed at the lower dose of 0.3 mg/g.

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Evidence for acutely hypoxic cells in mouse tumours, and a possible mechanism of reoxygenation

TL;DR: The proportion of viable hypoxic cells in EMT6/St/lu tumours assayed 18 and 24 hours after a dose of misonidazole was reduced, and the radiation cell-survival curve of the RIF-1 tumour was assayed in both intradermal and intramuscular sites under both air-breathing and acutely hypoxic conditions.
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SR-4233: a new bioreductive agent with high selective toxicity for hypoxic mammalian cells.

TL;DR: It is shown that the drug metabolizes more rapidly under hypoxic than aerobic conditions, both in vitro and in vivo, and could be a useful tool in tumor biology, as well as being a new lead in the development of bioreductive cytotoxic agents for cancer therapy.
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Review article: angiogenesis, neovascular proliferation and vascular pathophysiology as targets for cancer therapy.

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References
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Journal ArticleDOI

Tests of two electron-affinic radiosensitizers in vivo using regrowth of an experimental carcinoma.

TL;DR: Ro-07-0582 is the most effective sensitizer so far tested, giving an enhancement ratio of up to 2.1 when 1 mg/g is administered intraperitoneally, since no enhancement of well-oxygenated normal tissue has been observed.
Journal ArticleDOI

Demonstration of radiosensitization of hypoxic cells in solid tumours by metronidazole.

TL;DR: Significant radiosensitization of naturally occurring hypoxic cells by metronidazole (“Flagyl”) is demonstrated in two contrasting types of solid murine tumours, and at concentrations producing little toxicity, in first-generation transplanted mammary carcinomas in C3H mice.
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