BMP4 Inhibits Breast Cancer Metastasis by Blocking Myeloid-Derived Suppressor Cell Activity

被引:103
作者
Cao, Yuan [1 ]
Slaney, Clare Y. [1 ]
Bidwell, Bradley N. [1 ]
Parker, Belinda S. [2 ]
Johnstone, Cameron N. [1 ,3 ,4 ]
Rautela, Jai [1 ,5 ]
Eckhardt, Bedrich L. [6 ]
Anderson, Robin L. [1 ,3 ,7 ]
机构
[1] Peter MacCallum Canc Ctr, Div Res, East Melbourne, Vic, Australia
[2] La Trobe Univ, La Trobe Inst Mol Sci, Dept Biochem, Melbourne, Vic, Australia
[3] Univ Melbourne, Sir Peter MacCallum Dept Oncol, Parkville, Vic 3052, Australia
[4] Univ Melbourne, Dept Pharmacol, Parkville, Vic 3052, Australia
[5] Univ Melbourne, Dept Biochem, Parkville, Vic 3052, Australia
[6] Univ Texas MD Anderson Canc Ctr, Dept Breast Med Oncol, Morgan Welch Inflammatory Breast Canc Res & Clin, Houston, TX 77030 USA
[7] Univ Melbourne, Dept Pathol, Parkville, Vic 3052, Australia
基金
澳大利亚国家健康与医学研究理事会; 英国医学研究理事会;
关键词
COLONY-STIMULATING FACTOR; RETINOBLASTOMA PROTEIN; BONE METASTASIS; G-CSF; INFLAMMATION; INVASION; GROWTH; DOXORUBICIN; ASSOCIATION; RECRUITMENT;
D O I
10.1158/0008-5472.CAN-13-3171
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The TGF beta growth factor family member BMP4 is a potent suppressor of breast cancer metastasis. In the mouse, the development of highly metastatic mammary tumors is associated with an accumulation of myeloid-derived suppressor cells (MDSC), the numbers of which are reduced by exogenous BMP4 expression. MDSCs are undetectable in naive mice but can be induced by treatment with granulocyte colony-stimulating factor (G-CSF/Csf3) or by secretion of G-CSF from the tumor. Both tumor-induced and G-CSF-induced MDSCs effectively suppress T-cell activation and proliferation, leading to metastatic enhancement. BMP4 reduces the expression and secretion of G-CSF by inhibiting NF-kappa B (Nfkb1) activity in human and mouse tumor lines. Because MDSCs correlate with poor prognosis in patients with breast cancer, therapies based on activation of BMP4 signaling may offer a novel treatment strategy for breast cancer. (C) 2014 AACR.
引用
收藏
页码:5091 / 5102
页数:12
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