One dominant downstream effector pathway was the Cxcl1/Cxcr2 axis, as shown by inhibition of tumor growth by the Cxcr2 antagonist SB25002 (Fig. 3a), and the inability of EO771/shCxcl1 cells to sustain tumor proliferation in syngeneic mice (Fig. 4c). Here, CXCR2 is linked to neoplasm.