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Protection by Inhibitors of Multidrug Resistance Against Mitochondrial Mutagenesis in Saccharomyces Cerevisiae

Protection by Inhibitors of Multidrug Resistance Against Mitochondrial Mutagenesis in Saccharomyces Cerevisiae

B C Baguley, P M Turner, L R Ferguson

Eur J Cancer. 1990 Jan;26(1):55-60.

PMID: 2138480

Abstract:

A number of inhibitors thought to act on the drug efflux mechanism of multidrug-resistant cells have been tested for their ability to inhibit the induction of respiration-deficient (petite) colonies of the yeast Saccharomyces cerevisiae by mitochondrial mutagens. The mutagens tested were 3,6-diamino-9-(4-[(methylsulphonyl)aminophenyl]amino) acridine (an antitumour compound related to both amsacrine and proflavine), ethidium bromide, quinolinium dibromide (NSC 176319, a non-intercalative DNA binding antileukaemia agent) and rhodamine 123. The inhibitors tested included verapamil, perhexiline, chlorpromazine, trifluoperazine, reserpine, chloroquine, quinacrine, tamoxifen, clomiphene, cyclosporin A, valinomycin, amphotericin B and Tween 80. Several of these agents protected against mitochondrial mutagenesis, the most active being verapamil, reserpine, chloroquine, cyclosporin A and Tween 80. The correspondence between activity against multidrug resistance and activity in the yeast system strongly implies some degree of similarity in mechanisms for drug efflux from multidrug-resistant cells and drug uptake into the mitochondria of yeast. Agents protecting against the uptake of drugs into mitochondria of mammalian cells may have use in minimizing the long-term toxicity of anticancer drugs mediated by mitochondrial drug retention.

Chemicals Related in the Paper:

Catalog Number	Product Name	Structure	CAS Number	Price
AP1794554	Verapamil Related Compound B		1794-55-4	Price

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