Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1978 Jun;37(6):1026-32.
doi: 10.1038/bjc.1978.149.

A possible combination of hypoxic cell sensitizer with an oxic protector: implications for radiotherapy

Free PMC article

A possible combination of hypoxic cell sensitizer with an oxic protector: implications for radiotherapy

D Krishnan et al. Br J Cancer. 1978 Jun.
Free PMC article

Abstract

This paper discusses the results of experiments using γ-rays and a hypoxic sensitizer metronidazole (MET) and also a well-known protector, mercaptoethylamine (MEA), individually and in combination, on the survival of the yeast S. cerevisiae BZ 34. MET (5mM) gave a hypoxic enhancement ratio (ER) of 1·3. MEA (5mM, 10mM) gave a dose-modifying factor (DMF) of 1·9 and 2·3 respectively for euoxic cells. However, the DMFs for hypoxic cells were 1·0 and 1·1 for 5 and 10mM concentrations of MEA. A combination of 5mM MEA and 5mM MET gave a DMF of 2·0 for euoxic cells and the ER remained at 1·3 for hypoxic cells. The "effective" oxygen enhancement ratios were 2·3 and 1·7 for the control and the sensitizer respectively. In the combination this value was equal to or even slightly less than 1. All DMF, ER and OER values were derived from D(0) values of the survival curves. The values based on 10% survival are almost equal to those derived from D(0) values. All the survival curves gave the same extrapolation number, showing that the chemicals individually or in combination were truly dose-modifying.These results indicate that protectors such as MEA could be preferentially protecting euoxic cells, and that combining such "oxic protectors" with a hypoxic sensitizer could result in protecting euoxic cells while the sensitization of hypoxic cells was not much reduced. The implications of our results for radiotherapy are discussed. It appears that the use of nontoxic oxic protectors may be a useful adjuvant in overcoming the hypoxic-cell problem in radiotherapy.

PubMed Disclaimer

Similar articles

References

    1. Int J Radiat Biol. 1962 Apr;5:101-4 - PubMed
    1. Br J Radiol. 1959 Jan;32(373):18-21 - PubMed
    1. Int J Radiat Biol Relat Stud Phys Chem Med. 1977 Aug;32(2):145-52 - PubMed
    1. Radiat Res. 1977 May;70(2):433-43 - PubMed
    1. Cancer. 1977 Feb;39(2 Suppl):987-98 - PubMed

MeSH terms