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MET通路作为一个治疗靶点。

MET pathway as a therapeutic target.

作者信息

Kim Eric S, Salgia Ravi

机构信息

Section of Hematology/Oncology, Department of Medicine, University of Chicago Medical Center, Chicago, Illinois 60637, USA.

出版信息

J Thorac Oncol. 2009 Apr;4(4):444-7. doi: 10.1097/JTO.0b013e31819d6f91.

Abstract

Dysregulation of mesenchymal-epithelial transition factor receptor tyrosine kinase pathway leads to cell proliferation, protection from apoptosis, angiogenesis, invasion, and metastasis. It can be dysregulated through overexpression, constitutive activation, gene amplification, ligand-dependent activation or mutation. New drugs targeting various mesenchymal-epithelial transition factor pathways are being investigated with promising results.

摘要

间充质-上皮转化因子受体酪氨酸激酶通路的失调会导致细胞增殖、抗凋亡、血管生成、侵袭和转移。它可通过过表达、组成性激活、基因扩增、配体依赖性激活或突变而失调。目前正在研究针对各种间充质-上皮转化因子通路的新药,且取得了有前景的结果。

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本文引用的文献

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Molecular cancer therapy: can our expectation be MET?分子癌症治疗:我们的期望能够实现吗?
Eur J Cancer. 2008 Mar;44(5):641-51. doi: 10.1016/j.ejca.2008.01.022. Epub 2008 Mar 4.
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Experimental validation of miRNA targets.微小RNA(miRNA)靶标的实验验证
Methods. 2008 Jan;44(1):47-54. doi: 10.1016/j.ymeth.2007.09.005.
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