Luraghi Paolo, Schelter Florian, Krüger Achim, Boccaccio Carla
Division of Experimental Clinical Molecular Oncology, IRCC - Institute for Cancer Research and Treatment, University of Turin Medical School Candiolo, Italy.
Front Pharmacol. 2012 Sep 11;3:164. doi: 10.3389/fphar.2012.00164. eCollection 2012.
The MET proto-oncogene, encoding the tyrosine kinase receptor for Hepatocyte Growth Factor (HGF) regulates invasive growth, a genetic program that associates control of cell proliferation with invasion of the extracellular matrix and protection from apoptosis. Physiologically, invasive growth takes place during embryonic development, and, in post-natal life, in wound healing and regeneration of several tissues. The MET oncogene is overexpressed and/or genetically mutated in many tumors, thereby sustaining pathological invasive growth, a prerequisite for metastasis. MET is the subject of intense research as a target for small molecule kinase inhibitors and, together with its ligand HGF, for inhibitory antibodies. The tight interplay of MET with the protease network has unveiled mechanisms to be exploited to achieve effective inhibition of invasive growth.
MET原癌基因编码肝细胞生长因子(HGF)的酪氨酸激酶受体,它调节侵袭性生长,这是一种将细胞增殖控制与细胞外基质侵袭及抗凋亡保护联系起来的遗传程序。在生理情况下,侵袭性生长发生于胚胎发育期间,以及出生后的生命过程中,如伤口愈合和多种组织的再生过程。MET癌基因在许多肿瘤中过度表达和/或发生基因突变,从而维持病理性侵袭性生长,这是转移的一个先决条件。作为小分子激酶抑制剂的靶点,以及与其配体HGF一起作为抑制性抗体的靶点,MET是深入研究的对象。MET与蛋白酶网络的紧密相互作用揭示了可用于有效抑制侵袭性生长的机制。