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L. Polito, A. Bolognesi, P. L. Tazzari, V. Farini, C. Lubelli, et al., “The Conjugate Rituximab/Saporin-S6 Completely Inhibits Clonogenic Growth of CD20-Expressing Cells and Produces a Synergistic Toxic Effect with Fludarabine,” Leukemia, Vol. 18, No. 7, 2004, pp. 1215-1222. doi:10.1038/sj.leu.2403378

has been cited by the following article:

• TITLE: Saporin Conjugated Monoclonal Antibody to the Transcobalamin Receptor TCblR/CD320 Is Effective in Targeting and Destroying Cancer Cells

  AUTHORS: Edward V. Quadros, Yasumi Nakayama, Jeffrey M. Sequeira

  KEYWORDS: Transcobalamin Receptor; CD320 Gene; Cobalamin; Cancer; Toxin

  JOURNAL NAME: Journal of Cancer Therapy, Vol.4 No.6, July 22, 2013

  ABSTRACT: Cobalamin uptake into cells is mediated by the CD320 receptor for transcobalamin-bound cobalamin. Optimum receptor expression is associated with proliferating cells and therefore, in many cancers this receptor expression is up regulated. Delivering drugs or toxins via this receptor provides increased targeting to cancer cells while minimizing toxicity to the normal tissues. Saporin conjugated monoclonal antibodies to the extracellular domain of TCblR were effectively internalized to deliver a toxic dose of Saporin to some cancer cell lines propagating in culture. Antibody concentration of 2.5 nM was effective in producing optimum inhibition of cell proliferation. The cytotoxic effect of mAb-Saporin appears to be dictated primarily by the level of receptor expression and therefore normal primary cells expressing low levels of CD320 were spared while tumor cell lines with higher CD320 expression were destroyed. Targeting the pathway for cellular uptake of vitamin B12 via the CD320 receptor with toxin-antibody conjugates appears to be a viable treatment strategy for certain cancers that over expresses this receptor.