Antagonizing Integrin β3 Increases Immunosuppression in Cancer

Su, Xinming, Esser, Alison K, Amend, Sarah R, Xiang, Jingyu, Ross, Michael H, Fox, Gregory C, Kobayashi, Takayuki, Steri, Veronica, Roomp, Kirsten, Fontana, Francesca, Hurchla, Michelle A, Knolhoff, Brett L, Meyer, Melissa A, Morgan, Elizabeth A, Tomasson, Julia C, Novack, Joshua S, Zou, Wei, Faccio, Roberta, Novack, Deborah V, Robinson, Stephen D, Teitelbaum, Steven L, DeNardo, David G, Schneider, Jochen G and Weilbaecher, Katherine N (2016) Antagonizing Integrin β3 Increases Immunosuppression in Cancer. Cancer Research, 76 (12). pp. 3484-3495. ISSN 0008-5472

[img]
Preview
PDF (155984_1_merged_1455305305) - Submitted Version
Download (17MB) | Preview

Abstract

Integrin β3 is critical for tumor invasion, neoangiogenesis, and inflammation, making it a promising cancer target. However, preclinical and clinical data of integrin β3 antagonists have demonstrated no benefit or worse outcomes. We hypothesized that integrin β3 could affect tumor immunity and evaluated tumors in mice with deletion of integrin β3 in macrophage lineage cells (β3KOM). β3KOM mice had increased melanoma and breast cancer growth with increased tumor-promoting M2 macrophages and decreased CD8+ T cells. Integrin β3 antagonist, cilengitide, also enhanced tumor growth and increased M2 function. We uncovered a negative feedback loop in M2 myeloid cells, wherein integrin β3 signaling favored STAT1 activation, an M1-polarizing signal, and suppressed M2-polarizing STAT6 activation. Finally, disruption of CD8+ T cells, macrophages, or macrophage integrin β3 signaling blocked the tumor-promoting effects of integrin β3 antagonism. These results suggest that effects of integrin β3 therapies on immune cells should be considered to improve outcomes. Cancer Res; 76(12); 3484–95. ©2016 AACR.

Item Type: Article
Faculty \ School: Faculty of Science > School of Biological Sciences
Depositing User: Pure Connector
Date Deposited: 16 May 2016 14:00
Last Modified: 07 Oct 2019 09:30
URI: https://ueaeprints.uea.ac.uk/id/eprint/58749
DOI: 10.1158/0008-5472.CAN-15-2663

Actions (login required)

View Item View Item