Leflunomide, used for the treatment of rheumatoid arthritis, yields an active metabolite, A771726, which potently blocks pyrimidine synthesis by inhibiting dihydroorotate synthase. At higher concentrations, however, such as those used in this study, leflunomide inhibits AZD9291 purchase phosphorylation of PDGF receptor or EGF receptor (IC50 30–55 and 150–200 μM, respectively) [52]. The chemical screen described here also demonstrated a potential role for serotonin receptor 2B in regulating Hepcidin expression.

We found that SB 204741, a serotonin receptor 2B (5-HT2B) antagonist, increased Hepcidin expression and ID3 expression. Serotonin stimulates proliferation of hepatocellular carcinoma

cells [53], but represses liver regeneration via effects on hepatocyte stellate cells [54]. Animal studies indicate that the 5-HT2B inhibitor, SB 204741, confers the converse effect, decreasing growth of human hepatocellular carcinoma xenografts in mice [53], but enhancing liver regeneration following partial hepatectomy in animal models [54]. Daunorubicin, ethacridine lactate, phenazopyridine, and 9-aminoacridine each increased Hepcidin transcript levels and expression of the Stat3-dependent gene, SOCS3. As Stat3 is critically involved in liver injury and regeneration [55], it may be that these drugs stimulate Hepcidin expression by facilitating cell injury. Daunorubicin is an anti-cancer drug and DNA intercalator that inhibits Topoisomerase II resulting in breaks Thiamine-diphosphate kinase in double 5-FU manufacturer stranded DNA and increased apoptosis [56]. Daunorubicin has also been shown to increase expression of Stat3-dependent genes,

such as SOCS3 [57]. Ethacridine lactate provokes uterine contractions and histamine release [58], but also inhibits poly(ADP-ribose) glycohydrolase [59], the major enzyme that catabolizes poly(ADP-ribose). Inhibition of poly(ADP-ribose) glycohydrolase has been shown to promote apoptosis and impair DNA repair in cells damaged by oxidative stress [60]. Phenazopyridine can cause liver injury [61] and [62], while 9-aminoacridine is a DNA intercalator and experimental mutagen [63]. As a result of our screen, we have identified 16 small molecules that increase Hepcidin transcript levels in human HepG2 cells. Several of these chemicals affect growth factor receptor signaling, have anti-inflammatory properties, or impact DNA repair and apoptosis. The identification of multiple inhibitors of growth factor receptors and their downstream targets ( Fig. 5) indicates the importance of this pathway in regulating Hepcidin expression, while the discovery of inhibitors of histone deacetylase and serotonin receptor as Hepcidin stimulating agents indicates new avenues for further study.