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The PDZ protein TIP-1 facilitates cell migration and pulmonary metastasis of human invasive breast cancer cells in athymic mice
Han MJ1,2,3; Wang HL3; Zhang HT1; Han ZZ*3,4,5; zhaozhong.han@vanderbilt.edu
2012
发表期刊BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
卷号422期号:1页码:139-145
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摘要Tax-interacting protein 1 (TIP-1, also known as Tax1bp3) inhibited proliferation of colon cancer cells through antagonizing the transcriptional activity of beta-catenin. However, in this study, elevated TIP-1 expression levels were detected in human invasive breast cancers. Studies with two human invasive breast cancer cell lines indicated that RNAi-mediated TIP-1 knockdown suppressed the cell adhesion, proliferation, migration and invasion in vitro, and inhibited tumor growth in mammary fat pads and pulmonary metastasis in athymic mice. Biochemical studies showed that TIP-I knockdown had moderate and differential effects on the beta-catenin-regulated gene expression. but remarkably down regulated the genes for cell adhesion and motility in breast cancer cells. The decreased expression of integrins and paxillin was accompanied with reduced cell adhesion and focal adhesion formation on fibronectin-coated surface. In conclusion, this study revealed a novel oncogenic function of TIP-1 suggesting that TIP-1 holds potential as a prognostic biomarker and a therapeutic target in the treatment of human invasive breast cancers. (C) 2012 Elsevier Inc. All rights reserved.
关键词Tax-interacting Protein 1 Breast Cancer Beta-catenin Cell Adhesion Migration Pulmonary Metastasis
资助者This study was supported in part by NIH Grants R01CA127482 (Z. Han), P50CA128323 (J. Gore) and the Vanderbilt CTSA Grant RR024975-01 from NCRR/NIH ; This study was supported in part by NIH Grants R01CA127482 (Z. Han), P50CA128323 (J. Gore) and the Vanderbilt CTSA Grant RR024975-01 from NCRR/NIH ; This study was supported in part by NIH Grants R01CA127482 (Z. Han), P50CA128323 (J. Gore) and the Vanderbilt CTSA Grant RR024975-01 from NCRR/NIH ; This study was supported in part by NIH Grants R01CA127482 (Z. Han), P50CA128323 (J. Gore) and the Vanderbilt CTSA Grant RR024975-01 from NCRR/NIH
语种英语
资助者This study was supported in part by NIH Grants R01CA127482 (Z. Han), P50CA128323 (J. Gore) and the Vanderbilt CTSA Grant RR024975-01 from NCRR/NIH ; This study was supported in part by NIH Grants R01CA127482 (Z. Han), P50CA128323 (J. Gore) and the Vanderbilt CTSA Grant RR024975-01 from NCRR/NIH ; This study was supported in part by NIH Grants R01CA127482 (Z. Han), P50CA128323 (J. Gore) and the Vanderbilt CTSA Grant RR024975-01 from NCRR/NIH ; This study was supported in part by NIH Grants R01CA127482 (Z. Han), P50CA128323 (J. Gore) and the Vanderbilt CTSA Grant RR024975-01 from NCRR/NIH
WOS记录号WOS:000305046200025
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被引频次:8[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符http://ir.kiz.ac.cn/handle/152453/7079
专题分子免疫生物学
科研部门_动物模型与人类重大疾病机理重点实验室
通讯作者zhaozhong.han@vanderbilt.edu
作者单位1.Key Laboratory of Animal Models and Human Disease Mechanisms of the Chinese Academy of Sciences & Yunnan Province, Kunming Institute of Zoology, Yunnan, China
2.Graduate School, Chinese Academy of Sciences, Beijing, China
3.Department of Radiation Oncology, School of Medicine, Vanderbilt University, Nashville, TN 37232, USA
4.Department of Cancer Biology, School of Medicine, Vanderbilt University, Nashville, TN 37232, USA
5.Vanderbilt-Ingram Cancer Center, School of Medicine, Vanderbilt University, Nashville, TN 37232, USA
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Han MJ,Wang HL,Zhang HT,et al. The PDZ protein TIP-1 facilitates cell migration and pulmonary metastasis of human invasive breast cancer cells in athymic mice[J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS,2012,422(1):139-145.
APA Han MJ,Wang HL,Zhang HT,Han ZZ*,&zhaozhong.han@vanderbilt.edu.(2012).The PDZ protein TIP-1 facilitates cell migration and pulmonary metastasis of human invasive breast cancer cells in athymic mice.BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS,422(1),139-145.
MLA Han MJ,et al."The PDZ protein TIP-1 facilitates cell migration and pulmonary metastasis of human invasive breast cancer cells in athymic mice".BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 422.1(2012):139-145.
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