Shih Tsung-Chieh, Wang Lijun, Wang Hsiao-Chi, Wan Yu-Jui Yvonne
Department of Biochemistry and Molecular Medicine, University of California Davis, Sacramento, CA, USA.
Department of Pathology and Laboratory Medicine, University of California Davis, Sacramento, CA, USA.
Liver Res. 2020 Dec;4(4):168-172. doi: 10.1016/j.livres.2020.11.003. Epub 2020 Nov 11.
Hepatocellular carcinoma (HCC) is a malignant tumor with a fairly poor prognosis (5-year survival of less than 50%). Using sorafenib, the only food and drug administration (FDA)-approved drug, HCC cannot be effectively treated; it can only be controlled at most for a couple of months. There is a great need to develop efficacious treatment against this debilitating disease. Glypican-3 (GPC3), a member of the glypican family that attaches to the cell surface by a glycosylphosphatidylinositol anchor, is overexpressed in HCC cases and is elevated in the serum of a large proportion of patients with HCC. GPC3 expression contributes to HCC growth and metastasis. Furthermore, several different types of antibodies targeting GPC3 have been developed. The aim of this review is to summarize the current literatures on the GPC3 expression in human HCC, molecular mechanisms of GPC3 regulation and antibodies targeting GPC3.
肝细胞癌(HCC)是一种预后相当差的恶性肿瘤(5年生存率低于50%)。使用索拉非尼这种唯一获得美国食品药品监督管理局(FDA)批准的药物,HCC无法得到有效治疗;最多只能控制几个月。迫切需要开发针对这种使人衰弱疾病的有效治疗方法。磷脂酰肌醇蛋白聚糖-3(GPC3)是磷脂酰肌醇蛋白聚糖家族的成员,通过糖基磷脂酰肌醇锚定连接到细胞表面,在HCC病例中过度表达,并且在大部分HCC患者的血清中升高。GPC3表达促进HCC的生长和转移。此外,已经开发出几种针对GPC3的不同类型抗体。本综述的目的是总结关于GPC3在人类HCC中的表达、GPC3调控的分子机制以及针对GPC3的抗体的当前文献。