Laboratory of Genomics and Bioinformatics, Institute of Molecular Genetics, Academy of Science of the Czech Republic, Prague, Czech Republic.
Biol Cell. 2012 Dec;104(12):738-51. doi: 10.1111/boc.201200018.
Considering an analogy between wound healing and tumour progression, we studied chemokine and cytokine transcription and expression in normal fibroblasts by co-culture and in situ.
Whole-genome transcriptome profiling revealed strong upregulation for the interleukin (IL)-6, IL-8 and the chemokine CXCL-1 in in vitro co-cultures of normal fibroblasts with either normal or malignant epithelial cells compared to fibroblast cultures. The same ILs/chemokines were distinctly upregulated in clinical samples of squamous cell carcinoma when compared with paired normal mucosae. Analysis of culture supernatants showed that during the course of co-culture of the fibroblasts with the epithelial cells, IL-6, IL-8 and CXCL-1 were secreted to the culture medium. Experiments with addition of any of the proteins to the culture medium supported the notion that these ILs/chemokines strongly contributed to maintenance of a low-differentiation phenotype of epithelial cells, evaluated by the detection of keratin-8. Simultaneous addition of all factors increased the extent of the effect. These studies were extended by experiments with epithelial cells, either cultured in medium conditioned by preceding use for malignant keratinocytes without and in the presence of normal or cancer-associated fibroblasts or medium containing antibodies against IL-6, IL-8 and CXCL-1.
Our results indicate an analogy between wound healing and tumour growth, support the importance of epithelial-mesenchymal interaction in this model system and establish a potential bio-inspired anticancer therapy.
考虑到伤口愈合和肿瘤进展之间的类比,我们通过共培养和原位研究来研究正常成纤维细胞中的趋化因子和细胞因子转录和表达。
全基因组转录组谱分析显示,与成纤维细胞培养相比,正常成纤维细胞与正常或恶性上皮细胞的体外共培养中,白细胞介素 (IL)-6、IL-8 和趋化因子 CXCL-1 的表达明显上调。与配对的正常黏膜相比,鳞状细胞癌的临床样本中这些 IL/趋化因子明显上调。分析培养上清液表明,在成纤维细胞与上皮细胞共培养过程中,IL-6、IL-8 和 CXCL-1 被分泌到培养基中。向培养基中添加任何一种蛋白质的实验支持了这样一种观点,即这些 IL/趋化因子强烈有助于维持上皮细胞的低分化表型,通过检测角蛋白-8 来评估。同时添加所有因子会增加这种作用的程度。这些研究通过在没有和存在正常或癌相关成纤维细胞的情况下,用先前用于恶性角质形成细胞的培养基培养上皮细胞,或用含有针对 IL-6、IL-8 和 CXCL-1 的抗体的培养基进行实验得到了扩展。
我们的研究结果表明伤口愈合和肿瘤生长之间存在类比,支持上皮-间充质相互作用在该模型系统中的重要性,并建立了一种潜在的仿生抗癌治疗方法。