These compounds modulated the expression of a number of genes, such as: interferon 1 receptor, cytokine signaling, NFκB and ubiquitin protein lipase (inflammation), heat shock protein, RIKEN cDNA, ATPase, T cell receptor gamma (ageing), FAS, myosin, squalene epoxidase, NADH dehydrogenase, Prostaglandin D2 synthase, coagulation factor II (cardiovascular), and RAN, member of RAS oncogene family (cancer) as shown in Table 3. This evidence concerns the gene PTGDS and cancer.