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Glutathione transferase P1-1: self-preservation of an anti-cancer enzyme
- Source :
- Biochemical Journal. 376:71-76
- Publication Year :
- 2003
- Publisher :
- Portland Press Ltd., 2003.
-
Abstract
- Self-preservation is a typical property of living organisms, observed in the simplest prokaryotic cell as well as in the more complex pluricellular organisms. Surprisingly we found a self-preservation mechanism operating at the level of a single enzyme. Human glutathione transferase P1-1 operates in such a way towards either killer compounds (competitive and irreversible inhibitors) or physical factors (temperature and UV-rays), which could suppress its detoxicating and anti-cancer activity in the cell. This property, here termed ‘co-operative self-preservation’, is based on a structural intersubunit communication, by which one subunit, as a consequence of an inactivating modification, triggers a defence arrangement in the other subunit. Paradoxically this ability, developed during evolution for the survival of the cell, may not always be advantageous for us. In fact, glutathione transferase P1-1 is overexpressed in most tumour cells and pharmacological attempts to inhibit this enzyme in vivo, to prevent the drug resistance phenomenon during chemotherapy, may be thwarted by such self-preservation.
- Subjects :
- Models, Molecular
Protein subunit
Cell
Biology
Biochemistry
Isozyme
GPX6
In vivo
medicine
Humans
Computer Simulation
Enzyme Inhibitors
Settore BIO/10
Binding site
Molecular Biology
Glutathione Transferase
chemistry.chemical_classification
Binding Sites
Cell Biology
Isoenzymes
Protein Subunits
medicine.anatomical_structure
Enzyme
Glutathione S-Transferase pi
chemistry
Drug Resistance, Neoplasm
Research Article
Subjects
Details
- ISSN :
- 14708728 and 02646021
- Volume :
- 376
- Database :
- OpenAIRE
- Journal :
- Biochemical Journal
- Accession number :
- edsair.doi.dedup.....beda40e5b52140efa35b45a3584bd16d
- Full Text :
- https://doi.org/10.1042/bj20030860