Total synthesis of the potential anticancer vaccine KH-1 adenocarcinoma antigen Journal Article


Authors: Deshpande, P. P.; Danishefsky, S. J.
Article Title: Total synthesis of the potential anticancer vaccine KH-1 adenocarcinoma antigen
Abstract: Human tumours are often marked by the expression of unusual carbohydrate structural motifs. These carbohydrate domains are manifested as cell-surface bound glycolipids or glycoproteins. This raises the possibility of using cell-free equivalents of these domain compounds, obtained by total synthesis with a view towards triggering some level of immune response. In fact, the serum of mice immunized with fully synthetic compounds that mimic cell- surface tumour antigens has already been shown to recognize pertinent human cancer cell lines. Further advances in this field depend critically on the availability of these tumour-associated carbohydrate antigens which cannot be readily isolated from natural sources in sufficient quantities. Here we present the successful total synthesis of an adenocarcinoma antigen, KH-1, and of a bioconjugatable analogue which can bind to a carrier protein. These results illustrate the capabilities of oligosaccharide synthesis for reconstructing the challenging structural motifs characteristics of carbohydrate antigens, and thereby open up new possibilities for the development of anticancer vaccines.
Keywords: unclassified drug; adenocarcinoma; mass spectrometry; colonic neoplasms; drug structure; drug synthesis; tumor antigen; cancer inhibition; molecular sequence data; cancer vaccine; cancer vaccines; magnetic resonance spectroscopy; colon adenocarcinoma; nuclear magnetic resonance; antigens, tumor-associated, carbohydrate; carbohydrate sequence; carbohydrate antigen; glycolipid; carbohydrate conformation; humans; priority journal; article; carbohydrate metabolism; fucose; cancer vaccine kh 1
Journal Title: Nature
Volume: 387
Issue: 6629
ISSN: 0028-0836
Publisher: Nature Publishing Group  
Date Published: 1997-05-08
Start Page: 164
End Page: 166
Language: English
DOI: 10.1038/387164a0
PUBMED: 9144285
PROVIDER: scopus
DOI/URL:
Notes: Article -- Export Date: 17 March 2017 -- Source: Scopus
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