The tumor suppressor gene p53 is commonly mutated with high frequencies at certain hot spots in human cancers. In liver cancers there is an especially high frequency of mutations at codon 249. To study the impact of carcinogen targeting and the role of cytosine methylation on the mutation spectrum, a common liver cancer carcinogen aflatoxin B1 (AFB1), was studied using the p53 cDNA template to examine mutation induction. Subsequent mutations were detected with a yeast p53 functional assay and identified by DNA sequencing. The results indicated that cytosine methylation enhances AFB1-induced guanine mutations at CpG sites. However, no mutations were detected at codon 249. (C) 2003 Elsevier Ireland Ltd. All rights reserved
The tumor suppressor p53 exerts important protective functions towards DNA-damaging agents. Its inac...
The tumor suppressor p53 exerts important protective functions towards DNA-damaging agents. Its inac...
10.1016/S0165-1110(96)90005-6Mutation Research - Reviews in Genetic Toxicology366123-44MRRT
The tumor suppressor gene p53 is commonly mutated with high frequencies at certain hot spots in huma...
In liver cancer, aflatoxin B1 is a potent carcinogen and drug resistance is a major obstruction in c...
Mutations in the TP53 tumor suppressor gene are the most common alteration in cancer, and human prim...
Recent studies of the p53 tumor suppressor locus (designated TP53) in primary hepatocellular carcino...
Recent studies of the p53 tumor suppressor locus (designated TP53) in primary hepatocellular carcino...
Recent studies of the p53 tumor suppressor locus (designated TP53) in primary hepatocellular carcino...
Sequence-dependent formation and lack of repair of polycyclic aromatic hydrocarbon-induced DNA adduc...
Sequence-dependent formation and lack of repair of polycyclic aromatic hydrocarbon-induced DNA adduc...
The tumor suppressor p53 exerts important protective functions towards DNA-damaging agents. Its inac...
Background: Hepatocellular carcinoma (HCC) is a leading cause of cancer deaths. Aflatoxins, which ma...
Aflatoxin B1-induced DNA adduct formation and p53 mutations in CYP450-expressing human liver cell li...
The tumor suppressor p53 exerts important protective functions towards DNA-damaging agents. Its inac...
The tumor suppressor p53 exerts important protective functions towards DNA-damaging agents. Its inac...
The tumor suppressor p53 exerts important protective functions towards DNA-damaging agents. Its inac...
10.1016/S0165-1110(96)90005-6Mutation Research - Reviews in Genetic Toxicology366123-44MRRT
The tumor suppressor gene p53 is commonly mutated with high frequencies at certain hot spots in huma...
In liver cancer, aflatoxin B1 is a potent carcinogen and drug resistance is a major obstruction in c...
Mutations in the TP53 tumor suppressor gene are the most common alteration in cancer, and human prim...
Recent studies of the p53 tumor suppressor locus (designated TP53) in primary hepatocellular carcino...
Recent studies of the p53 tumor suppressor locus (designated TP53) in primary hepatocellular carcino...
Recent studies of the p53 tumor suppressor locus (designated TP53) in primary hepatocellular carcino...
Sequence-dependent formation and lack of repair of polycyclic aromatic hydrocarbon-induced DNA adduc...
Sequence-dependent formation and lack of repair of polycyclic aromatic hydrocarbon-induced DNA adduc...
The tumor suppressor p53 exerts important protective functions towards DNA-damaging agents. Its inac...
Background: Hepatocellular carcinoma (HCC) is a leading cause of cancer deaths. Aflatoxins, which ma...
Aflatoxin B1-induced DNA adduct formation and p53 mutations in CYP450-expressing human liver cell li...
The tumor suppressor p53 exerts important protective functions towards DNA-damaging agents. Its inac...
The tumor suppressor p53 exerts important protective functions towards DNA-damaging agents. Its inac...
The tumor suppressor p53 exerts important protective functions towards DNA-damaging agents. Its inac...
10.1016/S0165-1110(96)90005-6Mutation Research - Reviews in Genetic Toxicology366123-44MRRT