首页> 外文期刊>Growth Factors >Fibroblast growth factor 8 induced downregulation of thrombospondin 1 is mediated by the MEK/ERK and PI3K pathways in breast cancer cells.
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Fibroblast growth factor 8 induced downregulation of thrombospondin 1 is mediated by the MEK/ERK and PI3K pathways in breast cancer cells.

机译:成纤维细胞生长因子8诱导的血小板反应蛋白1的下调是由乳腺癌细胞中的MEK / ERK和PI3K途径介导的。

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摘要

Expression of fibroblast growth factor 8 (FGF-8) is increased in several forms of hormonal cancer. It was previously shown to regulate expression of thrombospondin 1 (TSP-1), an inhibitor of angiogenesis, in S115 breast cancer cells. Here, we studied the FGF-8-activated signalling pathways mediating TSP-1 repression in S115 cells and in non-tumorigenic MCF10A cells. Inhibition of FGF receptors or of MEK1/2 and PI3K with specific inhibitors (PD173074, U0126 or LY294002, respectively) restored TSP-1 mRNA expression in the presence of FGF-8 in S115 cells. Furthermore, U0126 and LY294002 increased TSP-1 mRNA expression in S115 cells over-expressing FGF-8. In MCF10A cells, FGF-8 treatment also decreased TSP-1 expression and the effect was dependent on active MEK1/2. In conclusion, FGF-8 suppresses TSP-1 expression through two independent pathways, MEK1/2 and PI3K. Repression of TSP-1 may be an important mechanism involved in induction of an angiogenic phenotype and growth of FGF-8-expressing breast cancer.
机译:在几种形式的激素癌中,成纤维细胞生长因子8(FGF-8)的表达增加。以前显示它可以调节S115乳腺癌细胞中的血小板生成素1(TSP-1)(一种血管生成抑制剂)的表达。在这里,我们研究了在S115细胞和非致瘤MCF10A细胞中介导TSP-1抑制的FGF-8激活信号通路。在S115细胞中存在FGF-8时,用特异性抑制剂(分别为PD173074,U0126或LY294002)抑制FGF受体或MEK1 / 2和PI3K可以恢复TSP-1 mRNA的表达。此外,U0126和LY294002在过表达FGF-8的S115细胞中增加了TSP-1 mRNA表达。在MCF10A细胞中,FGF-8处理还降低了TSP-1的表达,其作用取决于活性的MEK1 / 2。总之,FGF-8通过两个独立的途径MEK1 / 2和PI3K抑制TSP-1表达。 TSP-1的抑制可能是诱导血管生成表型和表达FGF-8的乳腺癌生长的重要机制。

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