O6-Methylguanine-DNA Methyltransferase in Normal and Malignant Tissue of the Breast
- 1 January 1994
- journal article
- research article
- Published by Taylor & Francis in Cancer Investigation
- Vol. 12 (6) , 605-610
- https://doi.org/10.3109/07357909409023045
Abstract
An important component of high-dose chemotherapy/autologous bone marrow support regimens for adjuvant treatment of breast cancer is carmustine. Preclinical studies have shown that the level of the DNA repair protein O6-methylguanine-DNA methyltransferase is correlated with the resistance of cultured human tumor cells to this drug, but little is known about transferase levels of breast tissue in vivo. We measured the DNA repair activity in 80 tissue samples from 65 patients, including normal, abnormal, benign, and malignant specimens. Wide interindividual variations was observed and average transferase levels were similar in normal and benign tissue. However, transferase levels were significantly elevated in stage I-IV disease. In addition, the frequency of samples with no detectable transferase was greatly reduced in this malignant group, and transferase was positively correlated with the presence of positive nodes, a marker for disease progression. In contrast, transferase levels were not correlated with age or estrogen receptor status, and the levels in normal tissue did not vary between patients with benign or malignant disease. These results suggest that this DNA repair activity may be increased in breast cancer relative to normal tissue and encourage further study of the predictive value of transferase measurements in high-dose chemotherapy/autologous bone marrow transplant for breast cancer.Keywords
This publication has 9 references indexed in Scilit:
- Cellular levels of O6-methylguanine-DNA methyltransferase in mammary epithelial cells and liver from virgin, pregnant and pituitary grafted miceCarcinogenesis: Integrative Cancer Research, 1991
- Depletion of mammalian O6-alkylguanine-DNA alkyltransferase activity by O6-benzylguanine provides a means to evaluate the role of this protein in protection against carcinogenic and therapeutic alkylating agents.Proceedings of the National Academy of Sciences, 1990
- Studies in gastric carcinogenesis. IV. O6-Methylguanine and its repair in normal and atrophic biopsy specimens of human gastric mucosa. Correlation of O6-alkylguanine-DNA alkyltransferase activities in gastric mucosa and circulating lymphocytesCarcinogenesis: Integrative Cancer Research, 1990
- Molecular analysis of O6-substituted guanine-induced mutagenesis of ras oncogenes.Proceedings of the National Academy of Sciences, 1989
- O6-Methylguanine methyltransferase increases before S phase in normal human cells but does not increase in hypermutable Bloom's syndrome cellsMutation Research Letters, 1986
- Comparison of O6-alkylguanine-DNA alkyltransferase activity based on cellular DNA content in human, rat and mouse tissuesCarcinogenesis: Integrative Cancer Research, 1986
- Induction of mammary carcinomas in rats by nitroso-methylurea involves malignant activation of H-ras-1 locus by single point mutationsNature, 1983
- DNA cross-linking and monoadduct repair in nitrosourea-treated human tumour cellsNature, 1980
- Persistence of O 6-Ethylguanine in Rat-Brain DNA: Correlation with Nervous System-Specific Carcinogenesis by EthylnitrosoureaProceedings of the National Academy of Sciences, 1974