Nedd9通过激活上皮-间质转化和肿瘤细胞迁移调控非小细胞肺癌的转移

Y. A. Topchu, A. Mazitova, M. V. Tikhomirova, Z. Abramova, A. Deneka
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引用次数: 2

摘要

非小细胞肺癌(NSCLC)生存率低,绝大多数死亡是由于转移所致。据报道,Nedd9蛋白(神经前体细胞表达,发育下调)在很大一部分肺癌和其他恶性肿瘤中表达升高,是侵袭性表型和耐药性的促进因子。本研究旨在确定Nedd9在转基因小鼠模型中调控非小细胞肺癌侵袭转移的机制。为了实现研究目标,我们利用磁共振成像(MRI)、组织免疫组化染色和显微镜、western blotting等方法进行了一系列体内和体外实验。我们发现Nedd9组成型零基因型在诱导型Kras / Trp53模型中促进肿瘤生长,在该模型中,吸入腺病毒特异性诱导Kras突变在肺组织中发生。组织病理学检查表明,Nedd9基因型也与较高的体内侵入能力相关,包括直接侵入心脏。我们进行了一系列实验来揭示发现的表型背后的机制。总的来说,我们的数据支持Nedd9为NSCLC早期生长提供关键支持的模型,并且在缺乏Nedd9的情况下,超过早期阶段的进展需要广泛的细胞内蛋白信号重编程,从而使肿瘤细胞获得间质特性,例如增加的移动性和侵袭性上皮-间质转化(EMT)。这些结果是新颖的,以前没有在文献中描述过。Nedd9调控非小细胞肺癌生长、侵袭和转移的生物学机制研究很少,其研究不仅具有基础意义-发现驱动肿瘤发展的新机制,而且具有重要的实际意义:评估非小细胞肺癌患者的Nedd9活性水平可能作为化疗反应的生物标志物。
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Nedd9 Regulates Metastasis of Non-Small Cell Lung Cancer through Activation of Epithelial-Mesenchymal Transition and Tumor Cells Migration
Non-small cell lung cancer (NSCLC) has a low survival rate, with metastasis contributing to the vast majority of deaths. Elevated expression of the protein Nedd9 (neural precursor cell expressed, developmentally down-regulated 9) has been reported in a large subset of lung cancers and other malignancies as a promotor of aggressive phenotypes and drug resistance. This study was performed to identify the mechanisms by which Nedd9 regulates invasion and metastasis of non-small cell lung cancer in the transgenic murine model. Aiming to address the research goals, we performed a set of in vivo and in vitro experiments with the help of such methods as magnetic resonance imaging (MRI), immunohistochemical staining of tissues and microscopy, western blotting. We found that Nedd9 constitutive null genotype enhanced tumor growth in an inducible Kras / Trp53 model, in which Kras mutation is induced specifically in the lung tissue by inhalation of adenovirus. Pathological examination of the tissues demonstrated that Nedd9 null genotype also was associated with higher invasive capacity in vivo , including direct invasion to the heart. We carried out a set of experiments to unveil the mechanism underlying the phenotype discovered. Overall, our data support the model in which Nedd9 provides critical support for early stages of the NSCLC growth, and progression beyond this early stage in the absence of Nedd9 requires extensive intracellular protein signaling reprogramming, allowing tumor cells to acquire mesenchymal properties, such as increased mobility and invasion epithelial-mesenchymal transition (EMT). These results are novel and have not been previously described in the literature. The biological mechanism by which Nedd9 regulates growth, invasion, and metastasis of NSCLC has been poorly investigated, and its study carries not only fundamental implication – discovery of novel mechanisms driving tumor development, but also significant practical importance: assessment of levels of Nedd9 activity in NSCLC patients can potentially serve as a biomarker of response to chemotherapy.
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