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作 者:Xin Chen Yongjie Zhu Lulu Han Hongting Lu Xiwei Hao Qian Dong
机构地区:[1]Department of Pediatric Surgery,the Affiliated Hospital of Qingdao University [2]Operating Room,the Affiliated Hospital of Qingdao University
出 处:《Neural Regeneration Research》2014年第10期1063-1067,共5页中国神经再生研究(英文版)
基 金:supported by the National Natural Science Foundation of China,No.81272986;the Natural Science Foundation of Shandong Province,No.ZR2011HZ002
摘 要:This study investigated the effects of small interfering RNA (siRNA)-mediated silencing of chemokine receptor 4 (CXCR4) on the invasion capacity of human neuroblastoma cell line SH-SY5Y in vitro. Three siRNAs targeting CXCR4 were chemically synthesized and individually transfected into SH-SY5Y cells. Expression of CXCR4 mRNA and protein was signiifcantly sup-pressed in transfected cells by all three sequence-speciifc siRNAs compared with control groups. Furthermore, the invasion capacity of SH-SY5Y cells was signiifcantly decreased following trans-fection with CXCR4-speciifc siRNA compared with the control groups. These data demonstrate that down-regulation of CXCR4 can inhibit in vitro invasion of neuroblastoma.This study investigated the effects of small interfering RNA (siRNA)-mediated silencing of chemokine receptor 4 (CXCR4) on the invasion capacity of human neuroblastoma cell line SH-SY5Y in vitro. Three siRNAs targeting CXCR4 were chemically synthesized and individually transfected into SH-SY5Y cells. Expression of CXCR4 mRNA and protein was signiifcantly sup-pressed in transfected cells by all three sequence-speciifc siRNAs compared with control groups. Furthermore, the invasion capacity of SH-SY5Y cells was signiifcantly decreased following trans-fection with CXCR4-speciifc siRNA compared with the control groups. These data demonstrate that down-regulation of CXCR4 can inhibit in vitro invasion of neuroblastoma.
关 键 词:nerve regeneration chemokine receptor 4 small interfering RNA NEUROBLASTOMA inva-sion Transwell chamber LIPOSOME NSFC grant neural regeneration
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