
doi: 10.1007/bf01963604
pmid: 6698179
The endoperoxide analogs known as U-46619 and U-44069 significantly enhanced the carcinoma formation and cellular atypicality initiated by a chemical carcinogen in mice. Studies of DNA radioactivity demonstrated that endoperoxides exerted their cocarcinogenic action by stimulating DNA synthesis. Thus, they play an important role in tumor cell proliferation.
DNA Replication, Male, Cocarcinogenesis, Prostaglandin Endoperoxides, Synthetic, Mice, Microscopy, Electron, Cell Transformation, Neoplastic, 15-Hydroxy-11 alpha,9 alpha-(epoxymethano)prosta-5,13-dienoic Acid, Carcinoma, Squamous Cell, Animals, Methylcholanthrene
DNA Replication, Male, Cocarcinogenesis, Prostaglandin Endoperoxides, Synthetic, Mice, Microscopy, Electron, Cell Transformation, Neoplastic, 15-Hydroxy-11 alpha,9 alpha-(epoxymethano)prosta-5,13-dienoic Acid, Carcinoma, Squamous Cell, Animals, Methylcholanthrene
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