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[Resistance associated with the glutathione system].

Authors: A, Gouyette;

[Resistance associated with the glutathione system].

Abstract

Several mechanisms of resistance (of bacteria to antibiotics, of plants to herbicides, of insects to insecticides, of cancer cells to cytotoxic agents...) have now been described. The most studied one is the glycoprotein coded by the mdr1 gene, which is involved in the efflux of numerous compounds of natural origin (anthracyclines, podophyllotoxins...) thus decreasing the intracellular concentration of such drugs. Nevertheless, many chemotherapeutic protocols include alkylating agents, such as cyclophosphamide and cisplatin, which are electrophilic species prone to react readily with the tripeptide glutathione, most often through glutathione-S-transferases. Therefore, it appears of major importance to evaluate the role of glutathione and that of the polymorphism of the glutathione-S-transferases, as prognostic factors in the response to chemotherapy.

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Keywords

Alkylating Agents, Antineoplastic Agents, Glutathione, Drug Resistance, Multiple, Nitrosourea Compounds, Humans, Chlorambucil, Mitoxantrone, Cyclophosphamide, Melphalan, Glutathione Transferase

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
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