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The role of c-MET inhibitors in advanced hepatocellular carcinoma: now and future

机译:C-Met抑制剂在晚期肝细胞癌中的作用:现在和未来

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摘要

Hepatocarcinogenesis is a complex biological process associated with several genetic and epigenetic alterations (1). Multiple molecular signaling pathways are critically involved in HCC carcinogenesis, such as Ras mitogen-activated protein kinase (Ras/Raf/MAPK), receptor tyrosine, phosphatidylinositol 3-kinase (PI3K)/AKT/mammalian target of rapamycin (mTOR), Wnt/β-catenin, Janus kinase-signal transducer activator of transcription factor (JAK/STAT), Hedgehog (HH) and Hippo (2). At present, systemic treatment approved for patients with advanced HCC are multitargeted drugs, including sorafenib, lenvatinib, regorafenib and cabozantinib, the immune checkpoint inhibitors (ICI) nivolumab and pembrolizumab, and the monoclonal VEGFR2 antibody ramucirumab (3-9).
机译:肝癌发生是一种与若干遗传和表观遗传改变(1)相关的复杂生物学过程。多种分子信号传导途径均可统称于HCC癌发生,例如RAS丝裂原激活蛋白激酶(RAS / RAF / MAPK),受体酪氨酸,磷脂酰肌醇3-激酶(PI3K)/ Akt /哺乳动物靶标雷帕霉素(MTOR),WNT / β-catenin,Janus激酶 - 信号传感器传感器转录因子(JAK / STAT),刺猬(HH)和Hippo(2)。目前,批准用于先进的HCC患者的全身治疗是多价药物,包括索拉非尼,Lenvatinib,RegoraFenib和Cabozantib,免疫检查点抑制剂(ICI)Nivolumab和Pembrolizumab,以及单克隆VEGFR2抗体Ramucirumab(3-9)。

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