Reference - Detail
| RRC ID | 1949 |
|---|---|
| Author | Selvendiran K, Koga H, Ueno T, Yoshida T, Maeyama M, Torimura T, Yano H, Kojiro M, Sata M. |
| Title | Luteolin promotes degradation in signal transducer and activator of transcription 3 in human hepatoma cells: an implication for the antitumor potential of flavonoids. |
| Journal | Cancer Res |
| Abstract |
In this study, we have investigated the underlying molecular mechanism for the potent proapoptotic effect of luteolin on human hepatoma cells both in vitro and in vivo, focusing on the signal transducer and activator of transcription 3 (STAT3)/Fas signaling. A clear apoptosis was found in the luteolin-treated HLF hepatoma cells in a time- and dosage-dependent manner. In concert with the caspase-8 activation by luteolin, an enhanced expression in functional Fas/CD95 was identified. Consistent with the increased Fas/CD95 expression, a drastic decrease in the Tyr(705) phosphorylation of STAT3, a known negative regulator of Fas/CD95 transcription, was found within 20 minutes in the luteolin-treated cells, leading to down-regulation in the target gene products of STAT3, such as cyclin D1, survivin, Bcl-xL, and vascular endothelial growth factor. Of interest, the rapid down-regulation in STAT3 was consistent with an accelerated ubiquitin-dependent degradation in the Tyr(705)-phosphorylated STAT3, but not the Ser(727)-phosphorylated one, another regulator of STAT3 activity. The expression level of Ser(727)-phosphorylated STAT3 was gradually decreased by the luteolin treatment, followed by a fast and clear down-regulation in the active forms of CDK5, which can phosphorylate STAT3 at Ser(727). An overexpression in STAT3 led to resistance to luteolin, suggesting that STAT3 was a critical target of luteolin. In nude mice with xenografted tumors using HAK-1B hepatoma cells, luteolin significantly inhibited the growth of the tumors in a dosage-dependent manner. These data suggested that luteolin targeted STAT3 through dual pathways-the ubiquitin-dependent degradation in Tyr(705)-phosphorylated STAT3 and the gradual down-regulation in Ser(727)-phosphorylated STAT3 through inactivation of CDK5, thereby triggering apoptosis via up-regulation in Fas/CD95. |
| Volume | 66(9) |
| Pages | 4826-34 |
| Published | 2006-5-1 |
| DOI | 10.1158/0008-5472.CAN-05-4062 |
| PII | 66/9/4826 |
| PMID | 16651438 |
| MeSH | Animals Antineoplastic Agents / pharmacology Apoptosis / drug effects Apoptosis / physiology Carcinoma, Hepatocellular / drug therapy* Carcinoma, Hepatocellular / metabolism Carcinoma, Hepatocellular / pathology Cell Growth Processes / drug effects Cell Line, Tumor Down-Regulation Humans Liver Neoplasms / drug therapy* Liver Neoplasms / metabolism Liver Neoplasms / pathology Luteolin / pharmacology* Male Mice Mice, Inbred BALB C Mice, Nude Phosphorylation / drug effects Receptors, Tumor Necrosis Factor, Type I / biosynthesis STAT3 Transcription Factor / biosynthesis STAT3 Transcription Factor / genetics STAT3 Transcription Factor / metabolism* Ubiquitin / metabolism Xenograft Model Antitumor Assays fas Receptor / biosynthesis |
| IF | 9.727 |
| Times Cited | 142 |
| WOS Category | ONCOLOGY |
| Altmetric score |
オルトメトリクス指標項目
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| The most frequently cited source | Patent(IFI CLAIMS) |
| Total number of mentions | 4 |
| Altmetric score changes over past 6months | 0.0 |
| Resource | |
| Human and Animal Cells | IMR-32(RCB1895) |