Gentile Alessandra, Trusolino Livio, Comoglio Paolo M
Division of Molecular Oncology, University of Turin Medical School, 10060, Candiolo (Torino), Italy.
Cancer Metastasis Rev. 2008 Mar;27(1):85-94. doi: 10.1007/s10555-007-9107-6.
Met is a tyrosine kinase receptor, encoded by an oncogene, whose crucial role has been elucidated during the last two decades. The complex biological program triggered by Met has been dissected and its biological relevance in both physiology and pathology has been proven. Met supports a morphogenetic program, known as invasive growth, taking place both during embryogenesis and adulthood. In tumors Met is often aberrantly activated, giving rise to the pathological counterpart of the invasive growth program: cancer progression towards metastasis. Several approaches have been recently developed to interfere with the tumorigenic and metastatic processes triggered by Met.
Met是一种由癌基因编码的酪氨酸激酶受体,在过去二十年中其关键作用已得到阐明。由Met触发的复杂生物学程序已被剖析,并且其在生理和病理过程中的生物学相关性也已得到证实。Met支持一种称为侵袭性生长的形态发生程序,该程序在胚胎发育和成年期均会发生。在肿瘤中,Met常常异常激活,从而引发侵袭性生长程序的病理对应物:癌症向转移的进展。最近已开发出几种方法来干扰由Met触发的致瘤和转移过程。