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The glutathione-related detoxification pathway in the human breast: a highly coordinated system disrupted in the tumour tissues

Identifieur interne : 002065 ( Istex/Checkpoint ); précédent : 002064; suivant : 002066

The glutathione-related detoxification pathway in the human breast: a highly coordinated system disrupted in the tumour tissues

Auteurs : Magali Perquin [France] ; Thierry Oster [France] ; Armand Maul [France] ; Nicolas Froment [France] ; Michel Untereiner [Luxembourg (pays)] ; Denyse Bagrel [France]

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RBID : ISTEX:9DCA06E2A566461DEA9BCE58E523BDF2B090522A

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Abstract

Abstract: Glutathione and the associated enzymes, glutathione S-transferases, peroxidases, and reductase, have been implicated in cancer chemoresistance. This pathway was investigated in paired cancerous and peritumoral breast samples from 41 women. The tumours exhibited a higher redox status as deduced from increased transferase, peroxidase, and reductase activities and from higher total and reduced glutathione contents. Several components were strongly correlated in peritumoral tissues, suggesting a highly co-ordinated glutathione pathway that appeared disrupted in breast tumours with only a few correlations left. Therefore, resistance could spontaneously result from deregulated variations in the glutathione pathway, which might be relevant to the malignant disease progression.

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DOI: 10.1016/S0304-3835(00)00481-X


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ISTEX:9DCA06E2A566461DEA9BCE58E523BDF2B090522A

Le document en format XML

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<div type="abstract" xml:lang="en">Abstract: Glutathione and the associated enzymes, glutathione S-transferases, peroxidases, and reductase, have been implicated in cancer chemoresistance. This pathway was investigated in paired cancerous and peritumoral breast samples from 41 women. The tumours exhibited a higher redox status as deduced from increased transferase, peroxidase, and reductase activities and from higher total and reduced glutathione contents. Several components were strongly correlated in peritumoral tissues, suggesting a highly co-ordinated glutathione pathway that appeared disrupted in breast tumours with only a few correlations left. Therefore, resistance could spontaneously result from deregulated variations in the glutathione pathway, which might be relevant to the malignant disease progression.</div>
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