Sundelin Kaarina, Roberg Karin, Grénman Reidar, Håkansson Leif
Department of Otorhinolaryngology-Head and Neck Surgery, University Hospital, Linköping, Sweden.
Acta Otolaryngol. 2005 Jul;125(7):765-73. doi: 10.1080/00016480510027484.
The intra-tumoral cytokines IL-6, hepatocyte growth factor (HGF) and tumour necrosis factor-a (TNF-a) stimulate oral cancer cells to enhanced secretion of matrix metalloproteinase (MMP)-1 and -9. These results contribute to an understanding of the extracellular events necessary for tumour progression.
MMPs play an important role in enhanced intra-tumoral proteolytic activity, promoting angiogenesis and invasion by acting on extracellular matrix substances. Cytokines secreted by tumour-infiltrating immune cells, fibroblasts and tumour cells can modulate MMP expression and secretion by cancer cells. The objective of this study was to investigate the effects of IL-6, soluble IL-6 receptor (sIL-6R), HGF, TNF-a and IL-8 on MMP-1, -2 and -9 expression by two oral squamous cell carcinoma cell lines (UT-SCC-20A and -24A).
ELISA was used to analyse secretion of total MMP protein and gelatin zymography was used for activity analysis.
IL-6 had a moderate stimulatory effect on MMP-1 secretion in both cell lines, whereas sIL-6R had no effect. When these cytokines were added together, a dose-dependent, synergistic stimulatory effect was observed. HGF also upregulated MMP-1 secretion, especially in one cell line (UT-SCC-24A), and a synergistic effect was observed when HGF was added to IL-6 in both cell lines. MMP-9 secretion by UT-SCC-24A was increased when stimulated with HGF and IL-6 combined with sIL-6R, whereas no effect was found in the other cell line. TNF-a stimulated MMP-9 secretion in both cell lines, but only stimulated MMP-1 secretion in one (UT-SCC-24A). The zymographic results were consistent with the ELISA results, indicating an upregulation of active enzyme when a stimulatory effect on protein expression was detected.
肿瘤内细胞因子白细胞介素-6(IL-6)、肝细胞生长因子(HGF)和肿瘤坏死因子-α(TNF-α)刺激口腔癌细胞增强基质金属蛋白酶(MMP)-1和-9的分泌。这些结果有助于理解肿瘤进展所需的细胞外事件。
基质金属蛋白酶在增强肿瘤内蛋白水解活性、促进血管生成和通过作用于细胞外基质物质进行侵袭方面发挥重要作用。肿瘤浸润免疫细胞、成纤维细胞和肿瘤细胞分泌的细胞因子可调节癌细胞中基质金属蛋白酶的表达和分泌。本研究的目的是调查IL-6、可溶性IL-6受体(sIL-6R)、HGF、TNF-α和IL-8对两种口腔鳞状细胞癌细胞系(UT-SCC-20A和-24A)中MMP-1、-2和-9表达的影响。
采用酶联免疫吸附测定法(ELISA)分析总基质金属蛋白酶蛋白的分泌,采用明胶酶谱法进行活性分析。
IL-6对两种细胞系中MMP-1的分泌均有中度刺激作用,而sIL-6R无作用。当将这些细胞因子一起添加时,观察到剂量依赖性的协同刺激作用。HGF也上调MMP-1的分泌,尤其是在一种细胞系(UT-SCC-24A)中,并且在两种细胞系中将HGF添加到IL-6中时均观察到协同作用。当用HGF和IL-6联合sIL-6R刺激时,UT-SCC-24A中MMP-9的分泌增加,而在另一种细胞系中未发现作用。TNF-α刺激两种细胞系中MMP-9的分泌,但仅刺激一种细胞系(UT-SCC-24A)中MMP-1的分泌。酶谱结果与ELISA结果一致,表明在检测到对蛋白表达有刺激作用时,活性酶上调。