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http://purl.uniprot.org/citations/21665146http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/21665146http://www.w3.org/2000/01/rdf-schema#comment"Tumor inflammation promotes angiogenesis, immunosuppression, and tumor growth, but the mechanisms controlling inflammatory cell recruitment to tumors are not well understood. We found that a range of chemoattractants activating G protein-coupled receptors (GPCRs), receptor tyrosine kinases (RTKs) and Toll-like/IL-1 receptors (TLR/IL1Rs) unexpectedly initiate tumor inflammation by activating the PI3-kinase isoform p110γ in Gr1+CD11b+ myeloid cells. Whereas GPCRs activate p110γ in a Ras/p101-dependent manner, RTKs and TLR/IL1Rs directly activate p110γ in a Ras/p87-dependent manner. Once activated, p110γ promotes inside-out activation of a single integrin, α4β1, causing myeloid cell invasion into tumors. Pharmacological or genetic blockade of p110γ suppressed inflammation, growth, and metastasis of implanted and spontaneous tumors, revealing an important therapeutic target in oncology."xsd:string
http://purl.uniprot.org/citations/21665146http://purl.org/dc/terms/identifier"doi:10.1016/j.ccr.2011.04.016"xsd:string
http://purl.uniprot.org/citations/21665146http://purl.uniprot.org/core/author"Hirsch E."xsd:string
http://purl.uniprot.org/citations/21665146http://purl.uniprot.org/core/author"Song X."xsd:string
http://purl.uniprot.org/citations/21665146http://purl.uniprot.org/core/author"Ginsberg M.H."xsd:string
http://purl.uniprot.org/citations/21665146http://purl.uniprot.org/core/author"Field S.J."xsd:string
http://purl.uniprot.org/citations/21665146http://purl.uniprot.org/core/author"Ellies L.G."xsd:string
http://purl.uniprot.org/citations/21665146http://purl.uniprot.org/core/author"Schmid M.C."xsd:string
http://purl.uniprot.org/citations/21665146http://purl.uniprot.org/core/author"Dippold H.C."xsd:string
http://purl.uniprot.org/citations/21665146http://purl.uniprot.org/core/author"Cheresh D.A."xsd:string
http://purl.uniprot.org/citations/21665146http://purl.uniprot.org/core/author"Acevedo L.M."xsd:string
http://purl.uniprot.org/citations/21665146http://purl.uniprot.org/core/author"Wrasidlo W."xsd:string
http://purl.uniprot.org/citations/21665146http://purl.uniprot.org/core/author"Avraamides C.J."xsd:string
http://purl.uniprot.org/citations/21665146http://purl.uniprot.org/core/author"Varner J.A."xsd:string
http://purl.uniprot.org/citations/21665146http://purl.uniprot.org/core/author"Foubert P."xsd:string
http://purl.uniprot.org/citations/21665146http://purl.uniprot.org/core/author"Blair S.L."xsd:string
http://purl.uniprot.org/citations/21665146http://purl.uniprot.org/core/author"Franco I."xsd:string
http://purl.uniprot.org/citations/21665146http://purl.uniprot.org/core/author"Manglicmot J.R."xsd:string
http://purl.uniprot.org/citations/21665146http://purl.uniprot.org/core/date"2011"xsd:gYear
http://purl.uniprot.org/citations/21665146http://purl.uniprot.org/core/name"Cancer Cell"xsd:string
http://purl.uniprot.org/citations/21665146http://purl.uniprot.org/core/pages"715-727"xsd:string
http://purl.uniprot.org/citations/21665146http://purl.uniprot.org/core/title"Receptor tyrosine kinases and TLR/IL1Rs unexpectedly activate myeloid cell PI3kgamma, a single convergent point promoting tumor inflammation and progression."xsd:string
http://purl.uniprot.org/citations/21665146http://purl.uniprot.org/core/volume"19"xsd:string
http://purl.uniprot.org/citations/21665146http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/21665146