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Precursor N-cadherin mediates glial cell line-derived neurotrophic factor-promoted human malignant glioma

机译:前体N-钙黏着蛋白介导神经胶质细胞源性神经营养因子促进的人类恶性神经胶质瘤

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摘要

As the most prevalent primary brain tumor, gliomas are highly metastatic, invasive and are characteristic of high levels of glial cell-line derived neurotrophic factor (GDNF). GDNF is an important factor for invasive glioma cell growth; however, the underlying mechanism involved is unclear. In this study, we affirm a significantly higher expression of the precursor of N-cadherin (proN-cadherin) in most gliomas compared with normal brain tissues. Our findings reveal that GDNF interacts with the extracellular domain of proN-cadherin, which suggests that proN-cadherin mediates GDNF-induced glioma cell migration and invasion. We hypothesize that proN-cadherin might cause homotypic adhesion loss within neighboring cells and at the same time promote heterotypic adhesion within the extracellular matrix (ECM) through a certain mechanism. This study also demonstrates that the interaction between GDNF and proN-cadherin activates specific intracellular signaling pathways; furthermore, GDNF promoted the secretion of matrix metalloproteinase-9 (MMP-9), which degrades the ECM via proN-cadherin. To reach the future goal of developing novel therapies of glioma, this study, reveals a unique mechanism of glioma cell migration and invasion.
机译:作为最普遍的原发性脑肿瘤,神经胶质瘤具有高度转移性,浸润性,并具有高水平的神经胶质细胞系衍生神经营养因子(GDNF)。 GDNF是侵袭性神经胶质瘤细胞生长的重要因素。但是,所涉及的潜在机制尚不清楚。在这项研究中,我们确认与正常脑组织相比,大多数神经胶质瘤中N-钙粘着蛋白前体(proN-钙粘着蛋白)的表达明显更高。我们的发现表明GDNF与proN-cadherin的胞外域相互作用,这表明proN-cadherin介导GDNF诱导的神经胶质瘤细胞迁移和侵袭。我们假设proN-钙粘着蛋白可能会导致邻近细胞内的同型粘附丧失,并同时通过某种机制促进细胞外基质(ECM)内的异型粘附。这项研究还表明,GDNF和proN-钙粘着蛋白之间的相互作用激活了特定的细胞内信号通路。此外,GDNF促进了基质金属蛋白酶9(MMP-9)的分泌,该酶通过proN-钙黏着蛋白降解ECM。为了达到开发新型神经胶质瘤疗法的未来目标,这项研究揭示了神经胶质瘤细胞迁移和侵袭的独特机制。

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