TY - JOUR
T1 - Direct contacts with colon cancer cells regulate the differentiation of bone marrow mesenchymal stem cells into tumor associated fibroblasts
AU - Peng, Yanan
AU - Li, Zongwei
AU - Yang, Peng
AU - Newton, Ian P.
AU - Ren, Hua
AU - Zhang, Lichao
AU - Wu, Haili
AU - Li, Zhuoyu
N1 - Copyright © 2014 Elsevier Inc. All rights reserved.
PY - 2014/8/15
Y1 - 2014/8/15
N2 - Tumor-stroma interactions are referred to as essential events in tumor progression. There has been growing attention that bone marrow-derived mesenchymal stem cells (BMSCs) can travel to tumor stroma, where they differentiate into tumor-associated fibroblast (TAF)-like cells, a predominant tumor-promoting stromal cell. However, little is definitively known about the contributors for this transition. Here, using an in vitro direct co-culture model of colon cancer cells and BMSCs, we identify that colon cancer cells can induce adjoining BMSCs to exhibit the typical characteristic of TAFs, with increased expression of a-smooth muscle actin (a-SMA). Importantly, the present data also reveals that activated Notch signaling mediates transformation of BMSCs to TAFs through the downstream TGF-ß/Smad signaling pathway.
AB - Tumor-stroma interactions are referred to as essential events in tumor progression. There has been growing attention that bone marrow-derived mesenchymal stem cells (BMSCs) can travel to tumor stroma, where they differentiate into tumor-associated fibroblast (TAF)-like cells, a predominant tumor-promoting stromal cell. However, little is definitively known about the contributors for this transition. Here, using an in vitro direct co-culture model of colon cancer cells and BMSCs, we identify that colon cancer cells can induce adjoining BMSCs to exhibit the typical characteristic of TAFs, with increased expression of a-smooth muscle actin (a-SMA). Importantly, the present data also reveals that activated Notch signaling mediates transformation of BMSCs to TAFs through the downstream TGF-ß/Smad signaling pathway.
U2 - 10.1016/j.bbrc.2014.07.074
DO - 10.1016/j.bbrc.2014.07.074
M3 - Article
C2 - 25063031
SN - 0006-291X
VL - 451
SP - 68
EP - 73
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 1
ER -