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
. 1997;76(7):870-7.
doi: 10.1038/bjc.1997.477.

Menadione-resistant Chinese hamster ovary cells have an increased capacity for glutathione synthesis

Affiliations
Free PMC article

Menadione-resistant Chinese hamster ovary cells have an increased capacity for glutathione synthesis

K A Vallis et al. Br J Cancer. 1997.
Free PMC article

Abstract

A cell line (MRc40) resistant to the model quinone compound, menadione, has been isolated from a parental Chinese hamster ovary cell line (CHO-K1). The known relationship between menadione toxicity and glutathione (GSH) depletion led us to investigate whether the mechanism of resistance of MRc40 was related to alteration in GSH homeostasis. Intracellular concentrations of GSH and cysteine (CySH) were twofold and 3.2-fold greater in MRc40 than in CHO-K1. Following exposure to menadione, GSH and CySH were depleted, but subsequent recovery of thiols was more rapid and of greater magnitude in MRc40 than in CHO-K1. Twelve hours after exposure to menadione, the concentrations of GSH and CySH were 9.7- and 4.2-fold greater in MRc40 than in CHO-K1. Using nuclear magnetic resonance (NMR) spectroscopy, we observed the in situ removal of menadione from cell suspensions of CHO-K1 and MRc40. However, only in CHO-K1 did we observe concomitant depletion of NMR-visible GSH. We conclude that the perturbation of GSH metabolism contributes to the resistant phenotype and is an important characteristic of menadione-resistant CHO cells.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Proc Natl Acad Sci U S A. 1981 Dec;78(12):7492-6 - PubMed
    1. J Biol Chem. 1975 Feb 25;250(4):1422-6 - PubMed
    1. Arch Biochem Biophys. 1984 Dec;235(2):343-50 - PubMed
    1. Radiat Res. 1985 Aug;103(2):232-9 - PubMed
    1. Cancer Treat Rev. 1985 Mar;12(1):49-63 - PubMed

Publication types