SOAT1 and neoplasm: In contrast, several signaling pathways that were previously reported to be critical to tumor development such as Wnt[9], Jak-Stat[14], MAPK[16], TGF beta[12] and others[18,20] demonstrated an enrichment of differentially regulated genes in only a few individual array experiments but not a significant or high overlap to genetic pathways enriched in embryonic development of the liver.