期刊
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
卷 379, 期 4, 页码 1027-1032出版社
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbrc.2009.01.009
关键词
Toll-like receptor 2; MDA-MB-231 cells; MCF-7 cells; Cell invasiveness; NF-kappa B
MDA MB-231 breast cancer cells have a high invasive potential, yet the mechanisms involved are [lot known. This study showed that Toll-like receptor 2 (TLR2) was highly expressed in MDA-MB-231 cells and played a critical role in cell invasion. Compared with the poorly invasive MCF-7 cells, MDA-MB-231 cells expressed 10.5-fold more TLR2. Using TLR2 agonist pg-LPS and TLR2 neutralizing antibody, We found that TLR2 activation significantly promoted MDA-MB-231 invasion, whereas TLR2 blockade diminished this capacity. TLR2 activation enhanced the activity of NF-kappa B and induced phosphorylation of TAK1 and I kappa B alpha in the TLR2/NF-kappa B signaling pathway in MDA-MB-231, but not in MCF-7 cells. TLR2 activation increased IL-6, TGF-beta, VEGF and MMP9 secretion, which are associated with TLR2-NF-kappa B signalling. We demonstrated that TLR2 is a critical receptor responsible for NF-KB signaling activity and highly invasive capacity of MDA-MB-231 cells. (C) 2009 Elsevier Inc. All rights reserved.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据