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首页> 外文期刊>PLoS One >Mesenchymal stem cells promote metastasis through activation of an ABL-MMP9 signaling axis in lung cancer cells
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Mesenchymal stem cells promote metastasis through activation of an ABL-MMP9 signaling axis in lung cancer cells

机译:间充质干细胞通过激活肺癌细胞的ABL-MMP9信号轴来促进转移

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Mesenchymal stem cells (MSCs) are recruited and activated by solid tumors and play a role in tumor progression and metastasis. Here we show that MSCs promote metastasis in a panel of non-small cell lung cancer (NSCLC) cells. MSCs elicit transcriptional alterations in lung cancer cells leading to increased expression of factors implicated in the epithelial-to-mesenchymal transition (EMT) and secreted proteins including matrix metalloproteinase-9 (MMP9). MSCs enhance secretion of enzymatically active MMP9 in a panel of lung adenocarcinoma cells. High expression of MMP9 is linked to low survival rates in lung adenocarcinoma patients. Notably, we found that ABL tyrosine kinases are activated in MSC-primed lung cancer cells and functional ABL kinases are required for MSC-induced MMP9 expression, secretion and proteolytic activity. Importantly, ABL kinases are required for MSC-induced NSCLC metastasis. These data reveal an actionable target for inhibiting MSC-induced metastatic activity of lung adenocarcinoma cells through disruption of an ABL kinase-MMP9 signaling axis activated in MSC-primed lung cancer cells.
机译:间充质干细胞(MSCs)被固体肿瘤募集和活化,并在肿瘤进展和转移中发挥作用。在这里,我们表明MSCs在非小细胞肺癌(NSCLC)细胞面板中促进转移。 MSCS引发肺癌细胞的转录改变,导致涉及在上皮 - 间充质转换(EMT)和分泌蛋白质中涉及的因素的表达增加,包括基质金属蛋白酶-9(MMP9)。 MSCs在肺腺癌细胞面板中增强酶活性MMP9的分泌。 MMP9的高表达与肺腺癌患者的低生存率相关联。值得注意的是,我们发现ABL酪氨酸激酶在MSC引发的肺癌细胞中激活,并且MSC诱导的MMP9表达,分泌和蛋白水解活性需要功能性ABR激酶。重要的是,MSC诱导的NSCLC转移需要ABL激酶。这些数据揭示了一种可动作的靶标,用于抑制MSC诱导的肺腺癌细胞的转移活性,通过破坏在MSC-灌注肺癌细胞中激活的ABL激酶-MMP9信号轴。

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