Apoptosis, Cancer and Development Laboratory-Equipe labellisée La Ligue-, CRCL UMR INSERM U1052 CNRS 5286, Université de Lyon, Centre Léon Bérard, 69008 Lyon, France.
Nat Rev Cancer. 2011 Mar;11(3):188-97. doi: 10.1038/nrc3005. Epub 2011 Feb 17.
Over the past few years, several genes, proteins and signalling pathways that are required for embryogenesis have been shown to regulate tumour development and progression by playing a major part in overriding antitumour safeguard mechanisms. These include axon guidance cues, such as Netrins and Slits. Netrin 1 and members of the Slit family are secreted extracellular matrix proteins that bind to deleted in colorectal cancer (DCC) and UNC5 receptors, and roundabout receptors (Robos), respectively. Their expression is deregulated in a large proportion of human cancers, suggesting that they could be tumour suppressor genes or oncogenes. Moreover, recent data suggest that these ligand-receptor pairs could be promising targets for personalized anticancer therapies.
在过去的几年中,已经发现许多胚胎发生所需的基因、蛋白质和信号通路通过在肿瘤发展和进展中发挥主要作用来调节肿瘤的发生和发展,从而克服抗肿瘤保护机制。这些通路包括轴突导向线索,如 Netrins 和 Slits。Netrin 1 和 Slit 家族成员是分泌的细胞外基质蛋白,分别与结直肠癌缺失(DCC)和 UNC5 受体以及绕路受体(Robos)结合。它们在很大一部分人类癌症中的表达失调,表明它们可能是肿瘤抑制基因或癌基因。此外,最近的数据表明,这些配体-受体对可能是个性化抗癌治疗的有希望的靶点。