Please use this identifier to cite or link to this item:
Title: Cancer cell CCL5 mediates bone marrow independent angiogenesis in breast cancer
Authors: Sax, Michael John;Gasch, Christin;Athota, Vineel Rag;Freeman, Ruth;Rasighaemi, Parisa;Westcott, David Elton;Day, Christopher John;Nikolic, Iva;Elsworth, Benjamin;Wei, Ming;Rogers, Kelly;Swarbrick, Alexander;Mittal, Vivek;Pouliot, Normand;Mellick, Albert Sleiman
Issue Date: 20-Dec-2016
EDate: 2016-12-20
Citation: Oncotarget 2016; 7(51): 85437-85449
Abstract: It has recently been suggested that the chemokine receptor (CCR5) is required for bone marrow (BM) derived endothelial progenitor cell (EPC) mediated angiogenesis. Here we show that suppression of either cancer cell produced CCL5, or host CCR5 leads to distinctive vascular and tumor growth defects in breast cancer. Surprisingly, CCR5 restoration in the BM alone was not sufficient to rescue the wild type phenotype, suggesting that impaired tumor growth associated with inhibiting CCL5/CCR5 is not due to defects in EPC biology. Instead, to promote angiogenesis cancer cell CCL5 may signal directly to endothelium in the tumor-stroma. In support of this hypothesis, we have also shown: (i) that endothelial cell CCR5 levels increases in response to tumor-conditioned media; (ii) that the amount of CCR5+ tumor vasculature correlates with invasive grade; and (iii) that inhibition of CCL5/CCR5 signaling impairs endothelial cell migration, associated with a decrease in activation of mTOR/AKT pathway members. Finally, we show that treatment with CCR5 antagonist results in less vasculature, impaired tumor growth, reduced metastases and improved survival. Taken as a whole, this work demonstrates that directly inhibiting CCR5 expressing vasculature constitutes a novel strategy for inhibiting angiogenesis and blocking metastatic progression in breast cancer.
DOI: 10.18632/oncotarget.13387
PubMed URL:
Type: Journal Article
Subjects: Angiogenesis
Breast cancer
Appears in Collections:Journal articles

Files in This Item:
There are no files associated with this item.

Items in AHRO are protected by copyright, with all rights reserved, unless otherwise indicated.