Breast Cancer Cells Induce Cancer-Associated Fibroblasts to Secrete Hepatocyte Growth Factor to Enhance Breast Tumorigenesis

被引:140
|
作者
Tyan, Shiaw-Wei [1 ]
Kuo, Wen-Hung [2 ]
Huang, Chun-Kai [1 ]
Pan, Chi-Chun [1 ]
Shew, Jin-Yuh [1 ]
Chang, King-Jen [2 ]
Lee, Eva Y. -H. P. [1 ,3 ,4 ]
Lee, Wen-Hwa [1 ,4 ]
机构
[1] Acad Sinica, Genom Res Ctr, Taipei 115, Taiwan
[2] Natl Taiwan Univ Hosp, Dept Surg, Taipei 100, Taiwan
[3] Univ Calif Irvine, Dept Dev & Cell Biol, Irvine, CA 92717 USA
[4] Univ Calif Irvine, Dept Biol Chem, Irvine, CA 92717 USA
来源
PLOS ONE | 2011年 / 6卷 / 01期
关键词
TUMOR-STROMAL INTERACTIONS; MICROENVIRONMENT; HETEROGENEITY; METASTASIS; CARCINOMAS; BETA; MET;
D O I
10.1371/journal.pone.0015313
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
It has been well documented that microenvironment consisting of stroma affects breast cancer progression. However, the mechanisms by which cancer cells and fibroblasts, the major cell type in stroma, interact with each other during tumor development remains to be elucidated. Here, we show that the human cancer-associated fibroblasts (CAFs) had higher activity in enhancing breast tumorigenecity compared to the normal tissue-associated fibroblasts (NAFs) isolated from the same patients. The expression level of hepatocyte growth factor (HGF) in these fibroblasts was positively correlated with their ability to enhance breast tumorigenesis in mice. Deprivation of HGF using a neutralizing antibody reduced CAF-mediated colony formation of human breast cancer cells, indicating that CAFs enhanced cancer cell colony formation mainly through HGF secretion. Co-culture with human breast cancer MDA-MB-468 cells in a transwell system enhanced NAFs to secret HGF as well as promote tumorigenecity. The newly gained ability of these "educated'' NAFs became irreversible after continuing this process till fourth passage. These results suggested that breast cancer cells could alter the nature of its surrounding fibroblasts to secrete HGF to support its own progression through paracrine signaling.
引用
收藏
页数:9
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