2011 Fiscal Year Final Research Report
Development of the new therapy targeted for pancreatic cancer stem cell and cancer cells with EMT status via induction of cellular senescence
Project/Area Number |
21590870
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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 |
Gastroenterology
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Research Institution | 地方独立行政法人宮城県立病院機構宮城県立がんセンター(研究所) (2011) Miyagi Cancer Center Research Institute (2010) Tohoku University (2009) |
Principal Investigator |
SATOH Kennichi 地方独立行政法人宮城県立病院機構宮城県立がんセンター(研究所), がん幹細胞研究部, 部長 (10282055)
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Co-Investigator(Kenkyū-buntansha) |
HAMADA Shin 東北大学, 病院, 医員 (20451560)
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Project Period (FY) |
2009 – 2011
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Keywords | 膵癌 / EMT / マイクロRNA |
Research Abstract |
The aim of this study was to identify the molecules to regulate EMT and the mechanism to control cellular senescence in pancreatic cancer. We revealed that miR 126 was down-regulated in invasive pancreatic cancer compared to non-invasive IPMN. In addition, the expression level of MSX2, inducer of EMT in pancreatic cancer, was found to be utilized for diagnosis of pancreatic cancer. Moreover, MSX2 expressing pancreatic cancer showed the chemoresistance, suggesting that EMT related molecules could be therapeutic target for pancreatic cancer.
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[Journal Article] Expression of MSX2 predicts malignancy of branch duct intraductal papillary mucinous neoplasm of the pancreas2010
Author(s)
Satoh K, Hamada S, Kanno A, Hirota M, Umino J, Ito H, Masamune A, Egawa S, Motoi F, Unno F, Shimosegawa T.
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Journal Title
J Gastoloenterol
Volume: 45
Pages: 763-70
Peer Reviewed
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