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Title: [The selective toxicity of 5-hydroxymethyldeoxyuridine for the cells of human adenocarcinoma of the large intestine]. Author: Lockshin A, Meshcherikova VV. Journal: Vopr Onkol; 1989; 35(11):1327-32. PubMed ID: 2609523. Abstract: Comparing the toxicities of potential anticancer agents for tumorous and normal cells derived from human intestinal epithelium may be a preferred approach for in vitro testing of compounds directed against colon carcinoma. 5-Hydroxymethyldeoxyuridine, a thymidine analog, was preferentially cytotoxic for two lines of human colon adenocarcinoma cells compared to a cell line derived from normal human fetal intestine. Unlike deoxyuridine and deoxycytydine, thymidine protected HT-29 human adenocarcinoma against 5-hydroxymethyldeoxyuridine toxicity, suggesting that thymidilate synthetase is the probable target enzyme of this thymidine analog. 5-Hydroxymethyldeoxyuridine may hold promise as an agent with specific activity against human adenocarcinoma cells.[Abstract] [Full Text] [Related] [New Search]