共 33 条
The Melanosomal Protein PMEL17 as a Target for Antibody Drug Conjugate Therapy in Melanoma
被引:19
作者:
Chen, Youjun
[1
]
Chalouni, Cecile
[2
]
Tan, Christine
[3
]
Clark, Robyn
[1
]
Venook, Rayna
[1
]
Ohri, Rachana
[3
]
Raab, Helga
[4
]
Firestein, Ron
[2
]
Mallet, William
[5
]
Polakis, Paul
[1
]
机构:
[1] Genentech Inc, Dept Res Oncol, San Francisco, CA 94080 USA
[2] Genentech Inc, Dept Pathol, San Francisco, CA 94080 USA
[3] Genentech Inc, Dept Antibody Engn, San Francisco, CA 94080 USA
[4] Genentech Inc, Dept Prot Chem, San Francisco, CA 94080 USA
[5] Novartis, Emeryville, CA 94608 USA
关键词:
CANCER-THERAPY;
PLASMID DNA;
MEMBRANE;
GLYCOPROTEIN;
MELANOCYTES;
ORGANELLES;
ENDOSOMES;
CLEAVAGE;
FRAGMENT;
CELLS;
D O I:
10.1074/jbc.M112.361485
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
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.
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页码:24082 / 24091
页数:10
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