Fernández-Zapico Martín E
Schulze Center for Novel Therapeutics, Division of Oncology Research, Mayo Clinic, Rochester, MN 55905, USA.
Pancreatology. 2008;8(3):227-9. doi: 10.1159/000134271. Epub 2008 May 22.
GLI proteins, highly conserved in vertebrates and invertebrates, are critical in modulating embryonic development and adult tissue homeostasis. These proteins are zinc-finger-containing transcription factors that were originally identified by genetic screening of embryonic lethal mutants of Drosophila melanogaster. Alterations in GLI activity can lead to tumor development in tissues of different origin including the pancreas. GLI activity is mainly regulated by the Hedgehog pathway, via a ligand-receptor complex that triggers a signaling cascade that activates GLI transcription factors, which in turn regulate gene expression, an essential step of Hedgehog-mediated cellular effects. Interestingly, recent reports show the ability of other signaling cascades to modulate GLI function in cancer cells including RAS and TGF-beta, two pathways implicated in pancreatic carcinogenesis. Thus, these findings suggest that GLI proteins are not an exclusive downstream target of Hedgehog but rather a common effector of a network of signaling pathways controlling pancreatic carcinogenesis. and IAP.
GLI蛋白在脊椎动物和无脊椎动物中高度保守,在调节胚胎发育和成年组织稳态方面至关重要。这些蛋白是含锌指的转录因子,最初是通过对黑腹果蝇胚胎致死突变体的遗传筛选鉴定出来的。GLI活性的改变可导致包括胰腺在内的不同起源组织发生肿瘤。GLI活性主要由Hedgehog信号通路调节,通过配体-受体复合物触发信号级联反应,激活GLI转录因子,进而调节基因表达,这是Hedgehog介导的细胞效应的关键步骤。有趣的是,最近的报道显示其他信号级联反应能够调节癌细胞中的GLI功能,包括RAS和TGF-β,这两条信号通路都与胰腺癌的发生有关。因此,这些发现表明GLI蛋白并非Hedgehog的唯一下游靶点,而是控制胰腺癌发生的信号通路网络的共同效应器。以及IAP。