Journal article

Tumour but not stromal expression of β 3 integrin is essential, and is required early, for spontaneous dissemination of bone-metastatic breast cancer

RZ Carter, KC Micocci, A Natoli, RP Redvers, S Paquet-Fifield, ACBM Martin, D Denoyer, X Ling, SH Kim, R Tomasin, H Selistre-De-Araújo, RL Anderson, N Pouliot

Journal of Pathology | Published : 2015

Abstract

Although many preclinical studies have implicated β3 integrin receptors (αvβ3 and αIIbβ3) in cancer progression, β3 inhibitors have shown only modest efficacy in patients with advanced solid tumours. The limited efficacy of β3 inhibitors in patients could arise from our incomplete understanding of the precise function of β3 integrin and, consequently, inappropriate clinical application. Data from animal studies are conflicting and indicate heterogeneity with respect to the relative contributions of β3-expressing tumour and stromal cell populations in different cancers. Here we aimed to clarify the function and relative contributions to metastasis of tumour versus stromal β3 integrin in clini..

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Funding Acknowledgements

We thank Dr SL Teitelbaum for providing beta 3 integrin-null mice and Ms Rachel Walker for assistance with subcutaneous injections. We acknowledge the kind donation of pLMP retroviral vector by Dr Ross Dickins (WEHI, Australia). This work was supported by the National Health and Medical Research Council (Project Grant No. 509131, to NP) and the National Breast Cancer Foundation (a postgraduate scholarship to RZC and a fellowship to RLA).