Department of Clinical Laboratory, Tianjin Huan Hu Hospital, Tianjin, 300060, China; Tianjin Key Laboratory of Cerebral Vessels and Neural Degeneration, Tianjin, 300060, China.
Anat Rec (Hoboken). 2013 Dec;296(12):1850-6. doi: 10.1002/ar.22821. Epub 2013 Oct 23.
The epithelial-mesenchymal transition (EMT) of tumor cells is deemed to be closely associated with tumor metastasis. CXCR4 has been proved to play an important role in the process of tumor metastasis. This study illustrates the function and expression of CXCR4 silencing and the EMT related genes in the human glioma cell line U87. The results showed that CXCR4 silencing could inhibit the cell invasive and adhesion potentials, expression of N-cadherin, vimentin, β-catenin, TGF-β1, p-Smad2, and p-Akt, and the activity of transcription factors NF-κB, AP-1, Snail, and twist. Meanwhile, CXCR4 silencing could also up-regulate the expression of E-cadherin, indicating that silencing of CXCR4 expression can inhibit the expression of EMT related genes in U87 cells. The study would provide a potential theoretical basis for the further exploration of the role of CXCR4 in human glioma.
肿瘤细胞的上皮-间充质转化(EMT)被认为与肿瘤转移密切相关。CXCR4 已被证明在肿瘤转移过程中发挥重要作用。本研究阐明了 CXCR4 沉默及其 EMT 相关基因在人神经胶质瘤细胞系 U87 中的功能和表达。结果表明,CXCR4 沉默可抑制细胞侵袭和黏附潜能,下调 N-钙黏蛋白、波形蛋白、β-连环蛋白、TGF-β1、p-Smad2 和 p-Akt 的表达,以及转录因子 NF-κB、AP-1、Snail 和 twist 的活性。同时,CXCR4 沉默还可上调 E-钙黏蛋白的表达,表明 CXCR4 表达沉默可抑制 U87 细胞中 EMT 相关基因的表达。本研究为进一步探索 CXCR4 在人神经胶质瘤中的作用提供了潜在的理论基础。