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. Author manuscript; available in PMC: 2018 Sep 1.
Published in final edited form as: Cancer Immunol Res. 2017 Aug 3;5(9):718–729. doi: 10.1158/2326-6066.CIR-16-0311

Figure 5. Schematic summarizing data and working hypotheses.

Figure 5

The following numbers refer to the number in the schematic. 1, Tgfbr2KO pancreatic epithelial cells secrete abundant CXCL1/CXCL5 due to lack of TGFβ suppression of chemokine expression (6). 2, The CXCL chemokines recruit to the tumor microenvironment myeloid cells (CD11b+). 3, In parallel with chemokines carcinoma cells secrete increased level of G-CSF. 4, G-CSF promotes differentiation of myeloid cells to Ly6G+ cells, upregulates immunosuppressive genes such as Arg, iNOS, VEGF and upregulate secretion of IL10 making (5) myeloid cells that are immunosuppressive with pro-tumorigenic properties. 6, The net result is enhanced tumor growth and decrease survival.