A new anticancer glycolipid monoclonal antibody, SC104, which directly induces tumor cell apoptosis

24Citations
Citations of this article
23Readers
Mendeley users who have this article in their library.

Abstract

A novel monoclonal antibody was raised by immunization of mice with colorectal tumor cell lines. The fusion was screened by inununohistochemistry for binding to primary colorectal tumors. Subsequent analysis on primary disaggregated colorectal tumors show that the antibody recognizes a cell surface antigen expressed by the majority of colorectal tumors. Antigen characterization has shown that the antibody recognizes a sialyltetraosylceramide but does not bind to GM1, GD1a, GT1b, or sialyl LewisX antigens. Binding to a frozen panel of tumor and normal tissue sections revealed that the antigen was also strongly expressed on esophageal, gastric, and endometrial tumors. Its normal tissue distribution was largely restricted to moderate staining of large intestine. Surprisingly, SC104 antibody directly induces tumor cell death without the need for immune effector cells or complement. This may be related in part to its homophilic binding properties that allow cross-linking of antibody and receptors on the cell surface. Caspase activation can be detected following SC104 treatment of colorectal cells, and cotreatment with caspase inhibitors has been shown to inhibit cell death. This suggests that SC104 induces death by a classic apoptotic pathway. Furthermore, SC104 antibody shows additive killing with complement and 5-fluorouracil/ leucovorin in vivo, suggesting a new therapeutic approach for this class of antibodies. ©2006 American Association for Cancer Research.

Cite

CITATION STYLE

APA

Durrant, L. G., Harding, S. J., Green, N. H., Buckberry, L. D., & Parsons, T. (2006). A new anticancer glycolipid monoclonal antibody, SC104, which directly induces tumor cell apoptosis. Cancer Research, 66(11), 5901–5909. https://doi.org/10.1158/0008-5472.CAN-05-3812

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free