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本文引用的文献

1
The overexpression of scaffolding protein NEDD9 promotes migration and invasion in cervical cancer via tyrosine phosphorylated FAK and SRC.支架蛋白 NEDD9 的过表达通过酪氨酸磷酸化 FAK 和 SRC 促进宫颈癌的迁移和侵袭。
PLoS One. 2013 Sep 18;8(9):e74594. doi: 10.1371/journal.pone.0074594. eCollection 2013.
2
Impact of the integrin signaling adaptor protein NEDD9 on prognosis and metastatic behavior of human lung cancer.整合素信号传导衔接蛋白 NEDD9 对人肺癌预后和转移行为的影响。
Clin Cancer Res. 2012 Nov 15;18(22):6326-38. doi: 10.1158/1078-0432.CCR-11-2162. Epub 2012 Oct 4.
3
Expression and clinical significance of NEDD9 in lung tissues.NEDD9 在肺组织中的表达及临床意义。
Med Oncol. 2012 Dec;29(4):2654-60. doi: 10.1007/s12032-012-0213-0. Epub 2012 Mar 24.
4
NEDD9 is a positive regulator of epithelial-mesenchymal transition and promotes invasion in aggressive breast cancer.NEDD9 是上皮-间充质转化的正向调节剂,可促进侵袭性乳腺癌的侵袭。
PLoS One. 2011;6(7):e22666. doi: 10.1371/journal.pone.0022666. Epub 2011 Jul 28.
5
NEDD9 and BCAR1 negatively regulate E-cadherin membrane localization, and promote E-cadherin degradation.NEDD9 和 BCAR1 负调控 E-钙黏蛋白的膜定位,促进 E-钙黏蛋白降解。
PLoS One. 2011;6(7):e22102. doi: 10.1371/journal.pone.0022102. Epub 2011 Jul 12.
6
Regulation of invasive behavior by vascular endothelial growth factor is HEF1-dependent.血管内皮生长因子通过 HEF1 调控侵袭行为。
Oncogene. 2010 Aug 5;29(31):4449-59. doi: 10.1038/onc.2010.185. Epub 2010 May 24.
7
NEDD9 promotes oncogenic signaling in mammary tumor development.NEDD9在乳腺肿瘤发展过程中促进致癌信号传导。
Cancer Res. 2009 Sep 15;69(18):7198-206. doi: 10.1158/0008-5472.CAN-09-0795. Epub 2009 Sep 8.
8
Nedd9/Hef1/Cas-L mediates the effects of environmental pollutants on cell migration and plasticity.Nedd9/Hef1/Cas-L介导环境污染物对细胞迁移和可塑性的影响。
Oncogene. 2009 Oct 15;28(41):3642-51. doi: 10.1038/onc.2009.224. Epub 2009 Aug 3.
9
Microenvironmental regulation of E-cadherin-mediated adherens junctions.E-钙黏蛋白介导的黏附连接的微环境调节
Front Biosci. 2008 May 1;13:3975-85. doi: 10.2741/2985.
10
Molecular basis for HEF1/NEDD9/Cas-L action as a multifunctional co-ordinator of invasion, apoptosis and cell cycle.HEF1/NEDD9/Cas-L作为侵袭、凋亡和细胞周期多功能协调因子发挥作用的分子基础。
Cell Biochem Biophys. 2007;48(1):54-72. doi: 10.1007/s12013-007-0036-3.

NEDD9的高表达预示着结直肠癌患者的不良预后。

High expression of NEDD9 predicts adverse outcomes of colorectal cancer patients.

作者信息

Li Peng, Zhou Houmin, Zhu Xinhong, Ma Guiliang, Liu Chao, Lin Bin, Mao Weizheng

机构信息

Department of General Surgery, Qingdao Municipal Hospital, Qingdao University Medical College Qingdao, China.

Department of International Clinic, Qingdao Municipal Hospital, Qingdao University Medical College Qingdao, China.

出版信息

Int J Clin Exp Pathol. 2014 Apr 15;7(5):2565-70. eCollection 2014.

PMID:24966970
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4069898/
Abstract

NEDD9, a member of Crk-associated substrate (CAS) family, is highly expressed in multiple cancer types and involved cancer cell adhesion, migration, invasion. The prognostic value of NEDD9 has not been evaluated before. The aim of this study was to evaluate the association between NEDD9 expression and survival in colorectal cancer (CRC) patients. NEDD9 expression was analyzed by immunohistochemistry in 92 patients with CRC. Patients were followed-up annually by telephone or at outpatient clinic. The results revealed that high expression of NEDD9 in 68/92 CRC samples, compared with 12/92 normal tissues (P<0.01). Correlation analysis showed high level of expression of NEDD9 was significantly correlated with advanced TNM stage (P=0.014), pT grade (P=0.009), pN (P=0.013) and pM status (P=0.047). Patients with a higher NEDD9 expression had a significantly shorter overall survival (OS) (P<0.01). The multivariate analysis revealed that NEDD9 expression could serve as an independent predictive factor of OS. Our finding demonstrated the potential value of NEDD9 expression level as a prognostic molecular marker and a target for new therapies for CRC patients.

摘要

NEDD9是Crk相关底物(CAS)家族的成员之一,在多种癌症类型中高表达,并参与癌细胞的黏附、迁移和侵袭。此前尚未评估过NEDD9的预后价值。本研究的目的是评估NEDD9表达与结直肠癌(CRC)患者生存率之间的关联。通过免疫组织化学分析了92例CRC患者的NEDD9表达情况。每年通过电话或门诊对患者进行随访。结果显示,68/92例CRC样本中NEDD9高表达,而正常组织中为12/92例(P<0.01)。相关性分析表明,NEDD9的高表达水平与晚期TNM分期(P=0.014)、pT分级(P=0.009)、pN(P=0.013)和pM状态(P=0.047)显著相关。NEDD9表达较高的患者总生存期(OS)显著缩短(P<0.01)。多变量分析显示,NEDD9表达可作为OS的独立预测因素。我们的研究结果证明了NEDD9表达水平作为CRC患者预后分子标志物和新治疗靶点的潜在价值。