| Literature DB >> 22613716 |
Youjun Chen1, Cecile Chalouni, Christine Tan, Robyn Clark, Rayna Venook, Rachana Ohri, Helga Raab, Ron Firestein, William Mallet, Paul Polakis.
Abstract
Melanocytes uniquely express specialized genes required for pigment formation, some of which are maintained following their transformation to melanoma. Here we exploit this property to selectively target melanoma with an antibody drug conjugate (ADC) specific to PMEL17, the product of the SILV pigment-forming gene. We describe new PMEL17 antibodies that detect the endogenous protein. These antibodies help define the secretory fate of PMEL17 and demonstrate its utility as an ADC target. Although newly synthesized PMEL17 is ultimately routed to the melanosome, we find substantial amounts accessible to our antibodies at the cell surface that undergo internalization and routing to a LAMP1-enriched, lysosome-related organelle. Accordingly, an ADC reactive with PMEL17 exhibits target-dependent tumor cell killing in vitro and in vivo.Entities:
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Year: 2012 PMID: 22613716 PMCID: PMC3397835 DOI: 10.1074/jbc.M112.361485
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157