| Literature DB >> 29241546 |
Julien Faget1, Svenja Groeneveld1, Gael Boivin2, Martial Sankar3, Nadine Zangger4, Miguel Garcia5, Nicolas Guex3, Inti Zlobec6, Loïc Steiner1, Alessandra Piersigilli7, Ioannis Xenarios3, Etienne Meylan8.
Abstract
Understanding the immune compartment of tumors facilitates the development of revolutionary new therapies. We used a Kras(G12D)-driven mouse model of lung cancer to establish an immune signature and identified a contribution of Gr1+ neutrophils to disease progression. Depletion experiments showed that Gr1+ cells (1) favor tumor growth, (2) reduce T cell homing and prevent successful anti-PD1 immunotherapy, and (3) alter angiogenesis, leading to hypoxia and sustained Snail expression in lung cancer cells. In turn, Snail accelerated disease progression and increased intratumoral Cxcl2 secretion and neutrophil infiltration. Cxcl2 was produced mainly by neutrophils themselves in response to a factor secreted by Snail-expressing tumor cells. We therefore propose a vicious cycle encompassing neutrophils and Snail to maintain a deleterious tumor microenvironment.Entities:
Keywords: CXCL2; MegaClust; PD1; Snail; hypoxia; immune exclusion; immunotherapy; lung cancer; neutrophil; vascularization
Mesh:
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Year: 2017 PMID: 29241546 DOI: 10.1016/j.celrep.2017.11.052
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423