Premium
TLR4 Promotes Breast Cancer Metastasis via Akt/GSK3β/β‐Catenin Pathway upon LPS Stimulation
Author(s) -
Li Jun,
Yin Jing,
Shen Wenzhi,
Gao Ruifang,
Liu Yanhua,
Chen Yanan,
Li Xiru,
Liu Chenghu,
Xiang Rong,
Luo Na
Publication year - 2017
Publication title -
the anatomical record
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.678
H-Index - 62
eISSN - 1932-8494
pISSN - 1932-8486
DOI - 10.1002/ar.23590
Subject(s) - stimulation , protein kinase b , cancer research , metastasis , catenin , breast cancer , medicine , oncology , breast cancer metastasis , cancer , phosphorylation , biology , signal transduction , wnt signaling pathway , microbiology and biotechnology , cancer metastasis
ABSTRACT Bacteria/virus‐induced chronic inflammation is involved in both tumor initiation and tumor progression. Toll‐like receptor 4 (TLR4) has been implicated in the development of several types of cancer. In this study, we explored the impact of TLR4 activation by lipopolysaccharide (LPS) on breast cancer metastasis and associated signaling molecules. We first examined TLR4 expression levels in breast tissue using a human breast tissue microarray and breast cell lines. We then studied the role of TLR4 activation by LPS stimulation in breast cancer metastasis using both in vitro and in vivo models. Finally, we investigated signaling molecules involved in the process using Western blotting and fluorescent immunohistochemistry staining. The results showed that TLR4 expression levels increased in breast cancer tissue compared to normal breast tissue. In addition, our results also showed that TLR4 pathway activation by LPS stimulation in MCF7 and MDA‐MB‐231 breast cancer cells caused the following actions: (1) promotes migration of breast cancer cells, (2) triggers the β‐catenin signaling pathway via PI3K/Akt/GSK3β, and (3) promotes transcription of downstream β‐catenin target genes leading to breast cancer metastasis. This study substantiates and further extends the relationship between TLR4 activation by LPS and breast cancer using both in vitro and in vivo models. The results suggest that the Akt/GSK3β/β‐catenin signal transduction pathway may serve as a viable clinical treatment target in breast cancer. Anat Rec, 300:1219–1229, 2017. © 2017 Wiley Periodicals, Inc.