Literature DB >> 12417795

Heterogeneity of O(6)-alkylguanine-DNA alkyltransferase activity in colorectal cancer: implications for treatment.

Nicholas P Lees1, Kathryn L Harrison, Elizabeth Hill, C Nicholas Hall, Andrew C Povey, Geoffrey P Margison.   

Abstract

OBJECTIVES: MGMT (O(6)-alkylguanine-DNA alkyltransferase) reverses the carcinogenic, mutagenic and cytotoxic effects of alkylating agents. Measurement of MGMT activity in tumours might thus be of use in selecting those patients with colorectal cancer who may be sensitive to adjuvant alkylating agent therapy. The aim of this study was to assess whether measurement of MGMT activity in a single tumour biopsy is representative of the whole tumour.
METHODS: Multiple symmetrically spaced biopsies were taken from colorectal cancers obtained from 9 patients. MGMT activity was then measured in cell-free extracts by quantifying the transfer of [(3)H]methyl group from calf thymus DNA methylated in vitro with N-nitroso-N-[(3)H]-methylurea to the MGMT protein.
RESULTS: MGMT activity was detected in all tumour samples with the activity ranging between 3.6 and 36.2 fmol/microg DNA and 202-1,986 fmol/mg protein. Heterogeneity in MGMT activity (ratio of maximum/minimum MGMT levels per tumour) varied between 1.3 and 5.4.
CONCLUSIONS: Measurement of MGMT activity in a single biopsy is not necessarily indicative of the level throughout the tumour. The response of colorectal cancers to alkylating agent treatment is likely to be non-uniform both within the tumour and between patients. Copyright 2002 S. Karger AG, Basel

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Year:  2002        PMID: 12417795     DOI: 10.1159/000066221

Source DB:  PubMed          Journal:  Oncology        ISSN: 0030-2414            Impact factor:   2.935


  3 in total

Review 1.  DNA alkylation and DNA methylation: cooperating mechanisms driving the formation of colorectal adenomas and adenocarcinomas?

Authors:  William M Grady; Cornelia M Ulrich
Journal:  Gut       Date:  2007-03       Impact factor: 23.059

2.  DNA damage induced by alkylating agents and repair pathways.

Authors:  Natsuko Kondo; Akihisa Takahashi; Koji Ono; Takeo Ohnishi
Journal:  J Nucleic Acids       Date:  2010-11-21

3.  O6-methylguanine-DNA-methyltransferase expression and gene polymorphisms in relation to chemotherapeutic response in metastatic melanoma.

Authors:  S Ma; S Egyházi; T Ueno; C Lindholm; E L Kreklau; U Stierner; U Ringborg; J Hansson
Journal:  Br J Cancer       Date:  2003-10-20       Impact factor: 7.640

  3 in total

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