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. Author manuscript; available in PMC: 2012 Feb 1.
Published in final edited form as: Mol Cancer Res. 2011 Jan 12;9(2):133–148. doi: 10.1158/1541-7786.MCR-10-0394

Figure 6.

Figure 6

A. Tumor volumes of ectopic MC38 tumors in wild type (n=10) and S100A9 null mice (n=12) 3 weeks after sc injection of 1×106 cells. 6 out of 12 S100A9 null mice showed significantly reduced tumor growth shown here. In addition, 2 of the remaining six S100A9 null mice completely rejected the tumors. B. CXCL1 in sera of wild type and S100A9 null mice before and 3 weeks after MC38 tumor growth. C. Quantitation of CD11b+ cells co-staining with Gr1 or GB3.1 glycans or RAGE from bone marrow of MC38 tumor-bearing wild type mice D. Tumors were examined for infiltrating macrophages and tumor endothelial cells by immunochemical staining for S100A9+ cells, CD11b+Gr1+ cells (merged images of Alexa-488 stained CD11b+ cells and Alexa-594 stained Gr1+ cells showing double positive yellow cells), and CD31+ and F4/80+ cells (200×). E. Representative sections showing CD11b+Gr1+ cells in premetastatic livers of tumor-free and tumor-bearing mice. F. Quantitation of average number of CD11b+Gr1+ cells in premetastatic livers in 3 high power fields.