TMC-264, a Novel Inhibitor of STAT6 Activation Produced by Phoma sp. TC 1674

A novel inhibitor of STAT6 activation, named as TMC-264 (1), was discovered from the fermentation broth of Phoma sp. TC 1674. Based on spectroscopic analyses, TMC-264 was found to be a novel tricyclic polyketide with chloro-1H-dibenzo[b, d]pyran-4, 6-dione. TMC-264 suppressed expression of IL-4 driv...

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Veröffentlicht in:Journal of antibiotics 2003/06/25, Vol.56(6), pp.513-519
Hauptverfasser: SAKURAI, MASAAKI, NISHIO, MAKI, YAMAMOTO, KOUZOU, OKUDA, TORU, KAWANO, KIMIO, OHNUKI, TETSUO
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Sprache:eng
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Zusammenfassung:A novel inhibitor of STAT6 activation, named as TMC-264 (1), was discovered from the fermentation broth of Phoma sp. TC 1674. Based on spectroscopic analyses, TMC-264 was found to be a novel tricyclic polyketide with chloro-1H-dibenzo[b, d]pyran-4, 6-dione. TMC-264 suppressed expression of IL-4 driven luciferase and germline Cε mRNA with IC50 values of 0.3μM and 0.4μM, respectively. TMC-264 exhibited a potent inhibitory activity against tyrosine phosphorylation of STAT6 with an IC50 value of 1.6μM, whereas TMC-264 weakly inhibited tyrosine phosphorylation of STAT5 with an IC50 value of 16μM, but did not inhibit the phosphorylation of STAT1 up to 40μM. TMC-264 blocked formation of the complexes between phosphorylated STAT6 and STAT6 oligonucleotides in a dose dependent manner, while TMC-264 did not affect the formation of phosphorylated STAT1/STAT1 oligonucleotides complexes. These results suggested that TMC-264 selectively inhibited IL-4 signaling by interfering both of phosphorylation of STAT6 and binding of the phosphorylated STAT6 to the recognition sequence.
ISSN:0021-8820
1881-1469
DOI:10.7164/antibiotics.56.513