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Therapeutic potential of targeting glypican-3 in hepatocellular carcinoma.

机译:靶向glypican-3在肝细胞癌中的治疗潜力。

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摘要

Glypican-3 (GPC3) is a developmentally-regulated oncofetal protein that has been established as a clinically-relevant biomarker for early hepatocellular carcinoma (HCC). It is one of the first transcripts to appear during malignant hepatocyte transformation, and is expressed at the protein level in approximately half of high-grade dysplastic macronodules in cirrhotic liver. Several studies show it is expressed in most (75 to 100%) of HCCs confirmed by histopathology. The protein is anchored to the hepatocyte membrane by a glycosyl-phosphatidylinositol (GPI) anchor and shows consistent membrane immunostaining pattern, making it a viable target for immunotherapeutic approaches. Targeting GPC3 for therapeutic intervention is a promising approach for the clinical management of HCC and selected other tumors that express the marker.
机译:Glypican-3(GPC3)是一种受发育调节的癌胚蛋白,已被确立为早期肝细胞癌(HCC)的临床相关生物标志物。它是在恶性肝细胞转化过程中出现的最早的转录物之一,在肝硬化肝脏中约一半的高级异常增生大结节中以蛋白质水平表达。几项研究表明,在组织病理学证实的大多数HCC中(75%至100%)它均表达。该蛋白通过糖基磷脂酰肌醇(GPI)锚定锚固在肝细胞膜上,并显示出一致的膜免疫染色模式,使其成为免疫治疗方法的可行靶标。将GPC3靶向进行治疗干预是对HCC和表达该标志物的选定其他肿瘤进行临床管理的有前途的方法。

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