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. 2021 Mar 16;22(6):3025. doi: 10.3390/ijms22063025

Figure 1.

Figure 1

Simplified overview of mutant-KRAS-dependent effects on the surrounding tumor microenvironment via direct cell-to-cell interactions and/or paracrine secretion of interleukins, GM-CSF and TGFβ. These paracrine signals induce the accumulation of myeloid-derived suppressor cells (MDSCs), M2-differentiated tumor-associated macrophages (TAMs) and regulatory T cells, which impair antitumor immunity by suppressing T-cell effector functions. References are displayed in brackets.