Compounds > 15-hydroxy-11-alpha-9-alpha-(epoxymethano)prosta-5-13-dienoic-acid

15-hydroxy-11-alpha-9-alpha-(epoxymethano)prosta-5-13-dienoic-acid and Cell-Transformation--Neoplastic

15-hydroxy-11-alpha-9-alpha-(epoxymethano)prosta-5-13-dienoic-acid has been researched along with Cell-Transformation--Neoplastic* in 1 studies

Other Studies

1 other study(ies) available for 15-hydroxy-11-alpha-9-alpha-(epoxymethano)prosta-5-13-dienoic-acid and Cell-Transformation--Neoplastic

Article	Year
Tumorigenic potential of endoperoxide analogs. Experientia, 1984, Feb-15, Volume: 40, Issue:2 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. Topics: 15-Hydroxy-11 alpha,9 alpha-(epoxymethano)prosta-5,13-dienoic Acid; Animals; Carcinoma, Squamous Cell; Cell Transformation, Neoplastic; Cocarcinogenesis; DNA Replication; Male; Methylcholanthrene; Mice; Microscopy, Electron; Prostaglandin Endoperoxides, Synthetic	1984

Article

Year

Tumorigenic potential of endoperoxide analogs.

Experientia, 1984, Feb-15, Volume: 40, Issue:2

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.

Topics: 15-Hydroxy-11 alpha,9 alpha-(epoxymethano)prosta-5,13-dienoic Acid; Animals; Carcinoma, Squamous Cell; Cell Transformation, Neoplastic; Cocarcinogenesis; DNA Replication; Male; Methylcholanthrene; Mice; Microscopy, Electron; Prostaglandin Endoperoxides, Synthetic

1984