Vannucci L
Laboratory of Immunotherapy, Institute of Microbiology, Academy of Sciences of the Czech Republic, v.v.i., Videnska 1083, 142 20, Prague 4, Czech Republic.
Laboratory of Tumor Biology, Institute of Animal Physiology and Genetics, Academy of Sciences of the Czech Republic, v.v.i., Rumburska 89, 277 21, Libechov, Czech Republic.
Cancer Microenviron. 2015 Dec;8(3):159-66. doi: 10.1007/s12307-014-0150-x. Epub 2014 Aug 9.
The stroma is a considerable part of the tumor microenvironment. Because of its complexity, it can influence both cancer and immune cells in their behavior and cross-talk. Aside from soluble products released by non-cancer and cancer cells, extracellular matrix components have been increasingly recognized as more than just minor players in the constitution, development and regulation of the tumor microenvironment. The variations in the connective scaffold architecture, induced by transforming growth factor beta, lysyl oxidase and metalloproteinase activity, create different conditions of ECM density and stiffness. They exert broad effects on immune cells (e.g. physical barriers, modulation by release of stored TGF-β1), mesenchymal cells (transition to myofibroblasts), epithelial cells (epithelial-to-mesenchymal transition), cancer cells (progression to metastatic phenotype) and stem cells (activation of differentiation addressed by the microenvironment characteristics). Physiological mechanisms of the wound healing process, as well as mechanisms of fibrosis in some chronic pathologies, closely recall aspects of cancer deregulated biology. Their elucidation can provide a better understanding of tumor microenvironment immunobiology. In the following short review, we will focus on some aspects of the fibrous stroma to highlight its active participation in the tumor microenvironment constitution, tumor progression and the local immunological network.
基质是肿瘤微环境的重要组成部分。由于其复杂性,它可以影响癌细胞和免疫细胞的行为及相互作用。除了非癌细胞和癌细胞释放的可溶性产物外,细胞外基质成分在肿瘤微环境的构成、发展和调节中所起的作用已越来越受到重视,而不仅仅是次要角色。由转化生长因子β、赖氨酰氧化酶和金属蛋白酶活性诱导的结缔组织支架结构变化,会产生细胞外基质密度和硬度的不同条件。它们对免疫细胞(如物理屏障、通过释放储存的TGF-β1进行调节)、间充质细胞(向肌成纤维细胞转变)、上皮细胞(上皮-间充质转化)、癌细胞(向转移表型进展)和干细胞(由微环境特征引发的分化激活)都有广泛影响。伤口愈合过程的生理机制以及某些慢性疾病中的纤维化机制,与癌症失调生物学的某些方面密切相关。对它们的阐明有助于更好地理解肿瘤微环境免疫生物学。在以下简短综述中,我们将聚焦于纤维基质的某些方面,以突出其在肿瘤微环境构成、肿瘤进展和局部免疫网络中的积极参与。