Guasch Géraldine, Schober Markus, Pasolli H Amalia, Conn Emily Belmont, Polak Lisa, Fuchs Elaine
Howard Hughes Medical Institute, The Rockefeller University, New York, NY 10021, USA.
Cancer Cell. 2007 Oct;12(4):313-27. doi: 10.1016/j.ccr.2007.08.020.
Although TGFbeta is a potent inhibitor of proliferation, epithelia lacking the essential receptor (TbetaRII) for TGFbeta signaling display normal tissue homeostasis. By studying asymptomatic TbetaRII-deficient stratified epithelia, we show that tissue homeostasis is maintained by balancing hyperproliferation with elevated apoptosis. Moreover, rectal and genital epithelia, which are naturally proliferative, develop spontaneous squamous cell carcinomas with age when TbetaRII is absent. This progression is associated with a reduction in apoptosis and can be accelerated in phenotypically normal epidermis by oncogenic mutations in Ras. We show that TbetaRII deficiency leads to enhanced keratinocyte motility and integrin-FAK-Src signaling. Together, these mechanisms provide a molecular framework to account for many of the characteristics of TbetaRII-deficient invasive SQCCs.
尽管转化生长因子β(TGFβ)是一种强大的增殖抑制剂,但缺乏TGFβ信号传导必需受体(TβRII)的上皮组织却表现出正常的组织稳态。通过研究无症状的TβRII缺陷型复层上皮,我们发现组织稳态是通过平衡过度增殖与凋亡增加来维持的。此外,直肠和生殖上皮天然具有增殖性,在缺乏TβRII的情况下,会随着年龄增长发生自发性鳞状细胞癌。这种进展与凋亡减少有关,并且在表型正常的表皮中,Ras基因的致癌突变可加速这一进程。我们发现,TβRII缺陷会导致角质形成细胞运动性增强以及整合素-FAK-Src信号传导增强。总之,这些机制提供了一个分子框架,用以解释TβRII缺陷型浸润性鳞状细胞癌(SQCCs)的许多特征。