| Project/Area Number |
21590845
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Gastroenterology
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| Research Institution | Osaka University |
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Principal Investigator |
HOSUI Atsushi 大阪大学, 医学系・研究科, 特任助教 (10536882)
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| Co-Investigator(Kenkyū-buntansha) |
TAKEHARA Tetsuo 大阪大学, 医学系・研究科, 教授 (70335355)
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| Project Period (FY) |
2009 – 2011
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| Project Status |
Completed (Fiscal Year 2011)
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| Budget Amount *help |
¥4,420,000 (Direct Cost: ¥3,400,000、Indirect Cost: ¥1,020,000)
Fiscal Year 2011: ¥780,000 (Direct Cost: ¥600,000、Indirect Cost: ¥180,000)
Fiscal Year 2010: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2009: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
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| Keywords | STAT1 / HCC / VEGF / IFN / HIF-1 / STAT3 / VEGD / 肝癌 / HAS2 |
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| Research Abstract |
Signal transducers and activators of transcription(STAT) 1 plays a pivotal role in cell-cycle and cell-fate determination, and vascular endothelial growth factor(VEGF) also contributes tumor growth. Recently interferon(IFN)αhas been reported to be effective for prevention of hepatocellular carcinomas(HCCs) recurrence, but the detailed mechanisms remain elusive. In vitro, cobalt chloride. treated VEGF induction and hypoxia responsive element(HRE) promoter activity were inhibited by IFNs and this abrogation was cancelled by introduction of small interfering RNA for STAT1. Immunoprecipitation/ Chromatin Immunoprecipitation analyses showed STAT1 bound to hypoxia-inducible factor(HIF)-1αand dissociated HIF-complex from HRE promoter lesion. In a xenograft model using Balb/ c nude mice, tumor growth was suppressed by IFNαthrough inhibition of VEGF expression and it was oppositely enhanced when STAT1-deleted cells were injected. This augmentation was due to upregulation of VEGF and hyaluronan synthase 2. In human samples, 29 HCCs were resected, divided into two groups based on STAT1 activation in tumor and the clinical features were investigated. Patients with suppressed STAT1 activity had a shorter recurrence-free survival. Histological and RT-PCR analyses showed portal vein microinvasion and increased VEGF levels in tumors from suppressed STAT1 group. These human samples also showed a reverse correlation between VEGF and STAT1-regulated genes expression. These results in vitro and in vivo suggested that IFNαare potential candidates for prevention of vessel invasion acting through inhibition of VEGF expression and need to be properly used when STAT1 expression is suppressed.
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