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Antibody and lectin target podoplanin to inhibit oral squamous carcinoma cell migration and viability by distinct mechanisms
Authors:Jhon A. Ochoa-Alvarez  Harini Krishnan  John G. Pastorino  Evan Nevel  David Kephart  Joseph J. Lee  Edward P. Retzbach  Yongquan Shen  Mahnaz Fatahzadeh  Soly Baredes  Evelyne Kalyoussef  Masaru Honma  Martin E. Adelson  Mika K. Kaneko  Yukinari Kato  Mary Ann Young  Lisa Deluca-Rapone  Alan J. Shienbaum  Kingsley Yin  Lasse D. Jensen  Gary S. Goldberg
Abstract:
Podoplanin (PDPN) is a unique transmembrane receptor that promotes tumor cell motility. Indeed, PDPN may serve as a chemotherapeutic target for primary and metastatic cancer cells, particularly oral squamous cell carcinoma (OSCC) cells that cause most oral cancers. Here, we studied how a monoclonal antibody (NZ-1) and lectin (MASL) that target PDPN affect human OSCC cell motility and viability. Both reagents inhibited the migration of PDPN expressing OSCC cells at nanomolar concentrations before inhibiting cell viability at micromolar concentrations. In addition, both reagents induced mitochondrial membrane permeability transition to kill OSCC cells that express PDPN by caspase independent nonapoptotic necrosis. Furthermore, MASL displayed a surprisingly robust ability to target PDPN on OSCC cells within minutes of exposure, and significantly inhibited human OSCC dissemination in zebrafish embryos. Moreover, we report that human OSCC cells formed tumors that expressed PDPN in mice, and induced PDPN expression in infiltrating host murine cancer associated fibroblasts. Taken together, these data suggest that antibodies and lectins may be utilized to combat OSCC and other cancers that express PDPN.
Keywords:podoplanin   cancer   cell migration   receptor   lectin
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