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pubmed-article:9685864pubmed:abstractTextMissile therapy, which destroys cancer cells specifically, has been advocated as an effective modality for the treatment of carcinoma. We have developed an immunoconjugate consisting of the monoclonal antibody MSN-1 (IgM), which reacts strongly with endometrial adenocarcinomas, combined with a plant hemitoxin named gelonin via a disulfide bond using N-succinimidyl-3-(2-pyridyldithio) propionate and 2-iminothiolane, and examined its selective cytotoxicity in athymic mice. The reductions in resected weights of target tumor cells, at the local site of MSN-1-gelonin immunoconjugate treatment, were 96% with local administration and 75% with caudal vein administration, as compared with the untreated group. There was no weight loss in treated mice. Our results suggest that this MSN-1-gelonin immunoconjugate has potential clinical applications in the treatment of endometrial adenocarcinomas.lld:pubmed
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pubmed-article:9685864pubmed:dateRevised2007-11-15lld:pubmed
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pubmed-article:9685864pubmed:articleTitleEffect of gelonin immunoconjugate with monoclonal antibody MSN-1 to endometrial adenocarcinoma on antigen-producing tumor cells in vivo.lld:pubmed
pubmed-article:9685864pubmed:affiliationDepartment of Obstetrics & Gynecology, Keio University School of Medicine, Tokyo.lld:pubmed
pubmed-article:9685864pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:9685864pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed