2012 Fiscal Year Final Research Report
Role of tumor-suppressive genes on LPS-induced inflammatory response
Project/Area Number |
22590408
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Bacteriology (including Mycology)
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Research Institution | Aichi Medical University |
Principal Investigator |
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Project Period (FY) |
2010 – 2012
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Keywords | LPS / ASAP1 / RAW264.7 NF-kappaB / 炎症性メディエーター |
Research Abstract |
The involvement of retinoblastoma protein-interacting zinc finger 1 (RIZ1), a tumor suppressor, in lipopolysaccharide (LPS)-induced inflammatory responses was investigated by using RAW 264.7 macrophage-like cells. RIZ1 was suggested to augment LPS-induced NF-kappaB activation in collaboration with p53 and enhance the production of proinflammatory cytokines in response to LPS. An ADP ribosylation factor-GTPase activating protein (ASAP1) is constitutively expressed in the cells and the expression was augmented by LPS stimulation. Silencing of ASAP1 enhanced the production of proinflammatory mediators in response to LPS. A series of tumor-associated genes are involved in LPS-induced inflammatory response in macrophages.
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[Journal Article] Retinoblastoma protein-interacting zinc finger 1, a tumor suppressor, augments lipopolysaccharide-induced proinflammatory cytokine production via enhancing nuclear factor-kappaB activation.2010
Author(s)
Noman AS, Koide N, Iftakhar-E-Khuda I, Dagvadorj J, Tumurkhuu G, Naiki Y, KomatsuT, Yoshida T, Yokochi T.
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Journal Title
Cell Immunol
Volume: 264
Pages: 114-8
DOI
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