| Literature DB >> 23471984 |
Mingqian Feng1, Wei Gao, Ruoqi Wang, Weizao Chen, Yan-Gao Man, William Douglas Figg, Xin Wei Wang, Dimiter S Dimitrov, Mitchell Ho.
Abstract
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.Entities:
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Year: 2013 PMID: 23471984 PMCID: PMC3607002 DOI: 10.1073/pnas.1217868110
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205