Olsen Jørgen, Kirkeby Lene T, Brorsson Marianne M, Dabelsteen Sally, Troelsen Jesper T, Bordoy Randi, Fenger Kirsten, Larsson Lars-Inge, Simon-Assmann Patricia
Department of Medical Biochemistry & Genetics, Biochemistry Laboratory C, University of Copenhagen, The Panum Institute Bldg. 6.4., Blegdamsvej 3, DK-2200N, Denmark.
Biochem J. 2003 Apr 1;371(Pt 1):211-21. doi: 10.1042/BJ20021454.
The trimeric extracellular matrix molecule laminin-5 and its constituent chains (alpha 3, beta 3, gamma 2) are normally not detectable intracellularly in intestinal epithelial cells but the laminin gamma 2 chain can be detected in cancer cells at the invasive front of a subset of colon carcinomas. These cells are subjected to cytokines such as transforming growth factor beta 1 (TGF-beta 1) and hepatocyte growth factor (HGF), produced by the tumour cells or by the surrounding stromal cells. The purpose of the present work was to investigate whether TGF-beta 1 and HGF, known to stimulate the LAMC2 gene encoding the laminin gamma 2 chain, might synergize to activate the LAMC2 promoter, and to identify the promoter elements involved. We find evidence for synergy between TGF-beta and HGF with respect to laminin gamma 2 chain expression and promoter activation and demonstrate that this requires the 5' activator protein-1 (AP-1) element of the promoter and an additional upstream element which is also responsive to co-expression of the Smad3 protein from the TGF-beta signalling pathway. The transcripts encoding the other laminin-5 chains are not synergistically activated by HGF and TGF-beta. Thus the synergistic activation of the LAMC2 gene is mediated via different cis-elements and results in an overproduction of the laminin gamma 2 chain relative to the other laminin-5 constituent chains. This difference may explain why laminin gamma 2 chains accumulate in the cells at the invasive front of colon carcinomas.
三聚体细胞外基质分子层粘连蛋白-5及其组成链(α3、β3、γ2)在正常情况下在肠上皮细胞内无法检测到,但在一部分结肠癌侵袭前沿的癌细胞中可检测到层粘连蛋白γ2链。这些细胞会受到肿瘤细胞或周围基质细胞产生的细胞因子如转化生长因子β1(TGF-β1)和肝细胞生长因子(HGF)的作用。本研究的目的是探讨已知能刺激编码层粘连蛋白γ2链的LAMC2基因的TGF-β1和HGF是否可能协同激活LAMC2启动子,并确定其中涉及的启动子元件。我们发现TGF-β和HGF在层粘连蛋白γ2链表达和启动子激活方面存在协同作用的证据,并证明这需要启动子的5'激活蛋白-1(AP-1)元件和另一个上游元件,该上游元件也对来自TGF-β信号通路的Smad3蛋白的共表达有反应。编码其他层粘连蛋白-5链的转录本不会被HGF和TGF-β协同激活。因此,LAMC2基因的协同激活是通过不同的顺式元件介导的,导致层粘连蛋白γ2链相对于其他层粘连蛋白-5组成链过量产生。这种差异可能解释了为什么层粘连蛋白γ2链会在结肠癌侵袭前沿的细胞中积累。