Human cancer antigen Globo H is a cell-surface ligand for human ribonuclease 1 Journal Article


Authors: Eller, C. H.; Chao, T. Y.; Singarapu, K. K.; Ouerfelli, O.; Yang, G.; Markley, J. L.; Danishefsky, S. J.; Raines, R. T.
Article Title: Human cancer antigen Globo H is a cell-surface ligand for human ribonuclease 1
Abstract: Pancreatic-type ribonucleases are secretory enzymes that catalyze the cleavage of RNA. Recent efforts have endowed the homologues from cow (RNase A) and human (RNase 1) with toxicity for cancer cells, leading to a clinical trial. The basis for the selective toxicity of ribonuclease variants for cancerous versus noncancerous cells has, however, been unclear. A screen for RNase A ligands in an array of mammalian cell-surface glycans revealed strong affinity for a hexasaccharide, Globo H, that is a tumor-associated antigen and the basis for a vaccine in clinical trials. The affinity of RNase A and RNase 1 for immobilized Globo H is in the low micromolar-high nanomolar range. Moreover, reducing the display of Globo H on the surface of human breast adenocarcinoma cells with a small-molecule inhibitor of biosynthesis or a monoclonal antibody antagonist decreases the toxicity of an RNase 1 variant. Finally, heteronuclear single quantum coherence (HSQC) NMR spectroscopy showed that RNase 1 interacts with Globo H by using residues that are distal from the enzymic active site. The discovery that a systemic human ribonuclease binds to a moiety displayed on human cancer cells links two clinical paradigms and suggests a mechanism for innate resistance to cancer.
Keywords: inhibitor; glycans; vaccines; expression; binding; monoclonal-antibody; tumor-associated antigen; human-breast; human pancreatic ribonuclease; mammalian ribonuclease
Journal Title: ACS Central Science
Volume: 1
Issue: 4
ISSN: 2374-7943
Publisher: American Chemical Society  
Date Published: 2015-07-22
Start Page: 181
End Page: 190
Language: English
ACCESSION: WOS:000365968300007
DOI: 10.1021/acscentsci.5b00164
PROVIDER: wos
PMCID: PMC4571170
PUBMED: 26405690
Notes: Article -- Source: Wos
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  1. Ouathek Ouerfelli
    100 Ouerfelli
  2. Guangbin Yang
    27 Yang