2011 Fiscal Year Final Research Report
Cancer therapy by vector co-expressing p53 and miRNA with RNA interference
Project/Area Number |
22790654
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Single-year Grants |
Research Field |
Gastroenterology
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Research Institution | Sapporo Medical University |
Principal Investigator |
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Project Period (FY) |
2010 – 2011
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Keywords | p53 / miRNA / MDM2 / p21 / アデノウイルスベクター / 癌 / アポトーシス |
Research Abstract |
We constructed adenovirus vector which express artificial miRNA targeting MDM2. Infection with this vector and vector which co-express p53 and artificial miRNA targeting p21 enhanced apoptosis more efficiently in cancer cells. This result suggests that adenovirus-mediated transduction of p53 and miRNAs targeting anti-apoptotic p53 target genes is useful for therapy of human cancers.
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[Journal Article] CHFR regulates the mitotic checkpoint by targeting PARP-1 for ubiquitination and degradation2012
Author(s)
Kashima L, Idogawa M, Mita H, Shitashige M, Yamada T, Ogi K, Suzuki H, Toyota M, Ariga H, Sasaki Y, Tokino T
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Journal Title
Journal of Biological Chemistry
Volume: (in press)
DOI
Peer Reviewed
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[Journal Article] p53 negatively regulates the hepatoma growth factor HDGF2011
Author(s)
Sasaki Y, Negishi H, Idogawa M, Yokota I, Koyama R, Kusano M, Suzuki H, Fujita M, Maruyama R, Toyota M, Saito T, Tokino T
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Journal Title
Cancer Research
Volume: 71(22)
Pages: 7038-47
DOI
Peer Reviewed
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