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Platelet-derived growth factor B induces senescence and transformation in normal human fibroblasts

机译:血小板衍生的生长因子B诱导正常人成纤维细胞衰老和转化

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摘要

Normal cells enter a senescent state upon aberrant oncogenic signals and this response inhibits tumor initiation and progression. It is now well admitted that intracellular and membrane localized oncogenes can illicit oncogene induced senescence. However, the effect of mitogenic growth factor on cellular senescence is so far largely unknown. Here we show that normal human dermal fibroblasts display a complex response to Platelet derived growth factor B (PDGFB) expression. Indeed, PDGFB expression induces, in the same cell population, both senescence and cellular transformation. Remarkably both populations are sustained with passages suggesting that transformed cells eventually enter a senescent state. This senescence state is p53 dependent as inhibiting the p53 pathway blocks the ability of PDGFB to induce senescence and results in strong cellular transformation increase upon PDGFB expression. The relevance of these observations is supported by the fact that human dermatofibrosarcoma protuberans, skin tumors arising from constitutive PDGFB production with little aggressiveness, also display some senescence hallmarks. Together these data support the view that PDGFB, a mitogenic growth factor, has a limited ability to induce senescence. We propose that this low level of senescence might decrease the transforming ability of this factor without totally abolishing it.
机译:正常细胞在异常的致癌信号下进入衰老状态,这种反应抑制了肿瘤的发生和发展。现在已经公认,细胞内和膜局部致癌基因可以使致癌基因非法衰老。然而,迄今为止,丝裂原生长因子对细胞衰老的影响尚不清楚。在这里,我们显示正常人真皮成纤维细胞显示出对血小板衍生生长因子B(PDGFB)表达的复杂反应。实际上,PDGFB表达在同一细胞群中诱导衰老和细胞转化。值得注意的是,两个种群均维持传代,表明转化的细胞最终进入衰老状态。该衰老状态是p53依赖性的,因为抑制p53途径会阻断PDGFB诱导衰老的能力,并导致PDGFB表达后细胞转化的强烈增加。这些观察结果的相关性得到了支持,即人皮纤维肉瘤隆突,即由组成型PDGFB产生而没有侵略性的皮肤肿瘤,也显示出一些衰老标志。这些数据一起支持以下观点,即促有丝分裂生长因子PDGFB诱导衰老的能力有限。我们认为这种低水平的衰老可能会降低该因子的转化能力,而不会完全消除它。

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