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Therapeutically targeting glypican-3 via a conformation-specific single-domain antibody in hepatocellular carcinoma
Author(s) -
Mingqian Feng,
Wei Gao,
Ruoqi Wang,
Weizao Chen,
YanGao Man,
William D. Figg,
Xin Wei Wang,
Dimiter S. Dimitrov,
Mitchell Ho
Publication year - 2013
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.1217868110
Subject(s) - glypican 3 , antibody , epitope , hepatocellular carcinoma , cancer research , chemistry , conformational epitope , cell , cancer , microbiology and biotechnology , biology , biochemistry , immunology , genetics
Glypican-3 (GPC3) has emerged as a candidate therapeutic target in hepatocellular carcinoma (HCC), but the oncogenic role of GPC3 in HCC is poorly understood. Here, we report a human heavy-chain variable domain antibody, HN3, with high affinity (Kd = 0.6 nM) for cell-surface-associated GPC3 molecules. The human antibody recognized a conformational epitope that requires both the amino and carboxy terminal domains of GPC3. HN3 inhibited proliferation of GPC3-positive cells and exhibited significant inhibition of HCC xenograft tumor growth in nude mice. The underlying mechanism of HN3 action may involve cell-cycle arrest at G1 phase through Yes-associated protein signaling. This study suggests a previously unrecognized mechanism for GPC3-targeted cancer therapy.

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