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首页> 外文期刊>Oncogene >DRR drives brain cancer invasion by regulating cytoskeletal-focal adhesion dynamics
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DRR drives brain cancer invasion by regulating cytoskeletal-focal adhesion dynamics

机译:DRR通过调节细胞骨架黏附动力学来驱动脑癌的侵袭

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摘要

Malignant glioma invasion is a primary cause of brain cancer treatment failure, yet the molecular mechanisms underlying its regulation remain elusive. We developed a novel functional-screening strategy and identified downregulated in renal cell carcinoma (DRR) as a regulator of invasion. We show that DRR drives invasion in vitro and in vivo. We found that while DRR is not expressed in normal glial cells, it is highly expressed in the invasive component of gliomas. Exploring underlying mechanisms, we show that DRR associates with and organizes the actin and microtubular cytoskeletons and that these associations are essential for focal adhesion (FA) disassembly and cell invasion. These findings identify DRR as a new cytoskeletal crosslinker that regulates FA dynamics and cell movement.
机译:恶性神经胶质瘤的侵袭是脑癌治疗失败的主要原因,但其调控的分子机制仍然难以捉摸。我们开发了一种新的功能筛选策略,并确定在肾细胞癌(DRR)中下调作为入侵的调节剂。我们表明DRR驱动体外和体内的入侵。我们发现,虽然DRR在正常的神经胶质细胞中不表达,但在胶质瘤的侵袭性成分中高度表达。探索潜在的机制,我们表明DRR关联并组织肌动蛋白和微管细胞骨架,这些关联对于粘着斑(FA)拆卸和细胞入侵至关重要。这些发现将DRR鉴定为调节FA动态和细胞运动的新型细胞骨架交联剂。

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