Laboratory of Molecular Biology, National Cancer Institute, Bethesda, MD 20892, USA.
Proc Natl Acad Sci U S A. 2013 Mar 19;110(12):E1083-91. doi: 10.1073/pnas.1217868110. Epub 2013 Mar 5.
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.
磷脂酰聚糖-3(GPC3)已成为肝细胞癌(HCC)的候选治疗靶点,但 GPC3 在 HCC 中的致癌作用仍知之甚少。在这里,我们报告了一种人源重链可变域抗体 HN3,它对细胞表面相关的 GPC3 分子具有高亲和力(Kd = 0.6 nM)。该人源抗体识别一个构象表位,该表位需要 GPC3 的氨基和羧基末端结构域。HN3 抑制了 GPC3 阳性细胞的增殖,并显著抑制了裸鼠 HCC 异种移植肿瘤的生长。HN3 作用的潜在机制可能涉及通过 Yes 相关蛋白信号通路使细胞周期停滞在 G1 期。这项研究为 GPC3 靶向癌症治疗提供了一个以前未被认识的机制。