Bierie Brian, Moses Harold L
Department of Cancer Biology, Vanderbilt University Medical Center, Nashville, TN, USA.
Cytokine Growth Factor Rev. 2006 Feb-Apr;17(1-2):29-40. doi: 10.1016/j.cytogfr.2005.09.006. Epub 2005 Nov 10.
TGF-beta signaling regulates tumorigenesis and in human cancer its signaling pathways are often modified during tumor progression. Prior to initiation and early during progression TGF-beta acts upon the epithelium as a tumor suppressor, however at later stages it is often a tumor promoter. Over the years, many studies have focused on the epithelial cell autonomous role for TGF-beta, however, TGF-beta is not strictly limited to this compartment in vivo. Recent studies addressing TGF-beta mediated stromal-epithelial interactions have significantly improved our understanding related to the regulation of cancer. In addition, stromal fibroblast cell autonomous effects have been observed in response to TGF-beta stimulation. According to the current literature and experimental evidence, TGF-beta is a potent ligand that regulates carcinoma initiation, progression and metastasis through a broad and complex spectrum of interdependent interactions.
转化生长因子-β(TGF-β)信号传导调节肿瘤发生,在人类癌症中,其信号通路在肿瘤进展过程中常常发生改变。在肿瘤起始之前及进展早期,TGF-β作为肿瘤抑制因子作用于上皮细胞,然而在后期它通常是肿瘤促进因子。多年来,许多研究聚焦于TGF-β在上皮细胞中的自主作用,然而,TGF-β在体内并不严格局限于这一区域。最近关于TGF-β介导的基质-上皮相互作用的研究显著增进了我们对癌症调控的理解。此外,已观察到基质成纤维细胞在TGF-β刺激下的自主效应。根据当前文献和实验证据,TGF-β是一种强效配体,通过广泛而复杂的相互依赖的相互作用谱来调节癌的起始、进展和转移。