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dc.contributor.authorMargison, Geoffrey P
dc.contributor.authorSantibanez-Koref, Mauro F
dc.date.accessioned2009-11-05T17:27:39Z
dc.date.available2009-11-05T17:27:39Z
dc.date.issued2002-03
dc.identifier.citationO6-alkylguanine-DNA alkyltransferase: role in carcinogenesis and chemotherapy. 2002, 24 (3):255-66 Bioessaysen
dc.identifier.issn0265-9247
dc.identifier.pmid11891762
dc.identifier.doi10.1002/bies.10063
dc.identifier.urihttp://hdl.handle.net/10541/85476
dc.description.abstractThe DNA in human cells is continuously undergoing damage as consequences of both endogenous processes and exposure to exogenous agents. The resulting structural changes can be repaired by a number of systems that function to preserve genome integrity. Most pathways are multicomponent, involving incision in the damaged DNA strand and resynthesis using the undamaged strand as a template. In contrast, O(6)-alkylguanine-DNA alkyltransferase is able to act as a single protein that reverses specific types of alkylation damage simply by removing the offending alkyl group, which becomes covalently attached to the protein and inactivates it. The types of damage that ATase repairs are potentially toxic, mutagenic, recombinogenic and clastogenic. They are generated by certain classes of carcinogenic and chemotherapeutic alkylating agents. There is consequently a great deal of interest in this repair system in relation to both carcinogenesis and cancer chemotherapy.
dc.language.isoenen
dc.subjectCanceren
dc.subject.meshAlkylating Agents
dc.subject.meshAnimals
dc.subject.meshCarcinogens
dc.subject.meshCell Transformation, Neoplastic
dc.subject.meshDNA Repair
dc.subject.meshHumans
dc.subject.meshNeoplasms
dc.subject.meshO(6)-Methylguanine-DNA Methyltransferase
dc.titleO6-alkylguanine-DNA alkyltransferase: role in carcinogenesis and chemotherapy.en
dc.typeArticleen
dc.contributor.departmentCRC Carcinogenesis Group, Paterson Institute for Cancer Research, Manchester, UK.en
dc.identifier.journalBioEssaysen
html.description.abstractThe DNA in human cells is continuously undergoing damage as consequences of both endogenous processes and exposure to exogenous agents. The resulting structural changes can be repaired by a number of systems that function to preserve genome integrity. Most pathways are multicomponent, involving incision in the damaged DNA strand and resynthesis using the undamaged strand as a template. In contrast, O(6)-alkylguanine-DNA alkyltransferase is able to act as a single protein that reverses specific types of alkylation damage simply by removing the offending alkyl group, which becomes covalently attached to the protein and inactivates it. The types of damage that ATase repairs are potentially toxic, mutagenic, recombinogenic and clastogenic. They are generated by certain classes of carcinogenic and chemotherapeutic alkylating agents. There is consequently a great deal of interest in this repair system in relation to both carcinogenesis and cancer chemotherapy.


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