Further downstream functional analysis of these targets showed substantial enrichments in the following Pathway Studio Ontologies: inflammatory cytokines (P<7.08E-19), extracellular matrix degradation proteins in general (7.66e-15), and matrix metalloproteinases in particular (2.66e-14), oncogenes (2.68e-14), adipokines (3.12e-10), lymphokines (5.18e-10), extracellular matrix polymerization proteins (6.52e-10), transcription factors of C/EBP family (1.31e-09), tumor suppressors (1.16e-08), and CSF-1/PDGF receptor family signals (1.89-e08). This evidence concerns the gene CSF1 and neoplasm.