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Deficient repair of DNA lesion O6-methylguanine in cirrhosis.

作者信息

Collier J D, Guo K, Burt A D, Bassendine M F, Major G N

机构信息

Department of Medicine, Medical School, University of Newcastle upon Tyne, UK.

出版信息

Lancet. 1993 Jan 23;341(8839):207-8. doi: 10.1016/0140-6736(93)90069-s.

Abstract

Cirrhosis is a risk factor for hepatocellular carcinoma. O6-methylguanine is a promutagenic and potentially carcinogenic DNA lesion produced by environmental alkylating agents. If it is not repaired, DNA replication can lead to a G-to-A transition mutation, which is a known mechanism of oncogene activation. We have found that the activity of the repairing methyltransferase enzyme is significantly lower in cirrhotic tissue than in non-cirrhotic diseased liver or in normal liver. This finding suggests a mechanism for cirrhosis being a risk factor for cancer of the liver: increased cellular proliferation together with persistence of O6-methylguanine might lead to malignant transformation of liver cells through mutation and oncogene activation.

摘要

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