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Nemosis, a novel way of fibroblast activation, in inflammation and cancer

机译:Nemosis,成纤维细胞激活的新颖方法,炎症和癌症

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Malignant cells when grown in suspension, as a rule, proliferate and can form spheroids that have been used as a model of tumor nodules, micrometastases and avascular tumors. In contrast, normal adherent cells cannot be stimulated to grow as multicellular aggregates. Now, recent results show that normal fibroblasts if forced to cluster (spheroid formation) do not grow but undergo a new pathway of cell activation (nemosis) leading to a massive proinflammatory, proteolytic and growth factor response. The clustering and activation are initiated by fibronectin-integrin interaction. The activated fibroblasts are able to modulate the behavior of cancer cells and, furthermore malignant cells boost this activation even further. In this model, the activation of fibroblasts terminates in programmed necrosis-like cell death. Activation of the tumor stroma, especially of fibroblasts, is of critical importance for tumor progression, although mechanisms leading to their activation are still largely uncharacterized. In summary, our results suggest that this kind of fibroblast activation (nemosis) may be involved in pathological conditions such as inflammation and cancer.
机译:恶性肿瘤细胞生长在暂停时,作为一个规则,增殖并能形成球状体已被用来作为模型的肿瘤结节,微转移和无血管的肿瘤。相反,贴壁细胞不能正常刺激增长多细胞聚集。现在,最近的结果表明,正常成纤维细胞如果被迫集群(球体形成)成长,但经过细胞激活的新途径(nemosis)导致大量的促炎,蛋白水解和生长因子响应。由聚类和激活fibronectin-integrin交互。成纤维细胞能够调节的行为癌细胞,而且恶性细胞进一步提高这个激活。模型中,成纤维细胞的激活终止在necrosis-like细胞程序性死亡。激活的肿瘤间质,尤其是成纤维细胞,肿瘤是至关重要的导致他们的进展,尽管机制激活仍但一个个。总结,我们的结果表明,这类成纤维细胞激活(nemosis)可能参与其中在病理条件下,如炎症和癌症。

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