Induction of tumor-suppressing pancreatic stellate cell subpopulation by pancreatic cancer microenvironment reprogramming
Project/Area Number |
15H04933
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Research Category |
Grant-in-Aid for Scientific Research (B)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Digestive surgery
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Research Institution | Kyushu University |
Principal Investigator |
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Co-Investigator(Kenkyū-buntansha) |
井上 重隆 九州大学, 医学研究院, 共同研究員 (00529802)
大内田 研宙 九州大学, 大学病院, 講師 (20452708)
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Project Period (FY) |
2015-04-01 – 2018-03-31
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Project Status |
Completed (Fiscal Year 2017)
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Budget Amount *help |
¥16,640,000 (Direct Cost: ¥12,800,000、Indirect Cost: ¥3,840,000)
Fiscal Year 2017: ¥5,460,000 (Direct Cost: ¥4,200,000、Indirect Cost: ¥1,260,000)
Fiscal Year 2016: ¥5,330,000 (Direct Cost: ¥4,100,000、Indirect Cost: ¥1,230,000)
Fiscal Year 2015: ¥5,850,000 (Direct Cost: ¥4,500,000、Indirect Cost: ¥1,350,000)
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Keywords | 膵臓癌 / 膵星細胞 / 癌微小環境 / 膵癌間質reprogramming / 腫瘍抑制性膵星細胞 / desmoplasia / 抗線維化薬 / 膵癌 / reprogramming |
Outline of Final Research Achievements |
We identified subpopulation of CD51 highly expressed pancreatic stellate cells as tumor-promoting pancreatic stellate cells and CD146 highly expressed pancreatic stellate cells as tumor-suppressing pancreatic stellate cells. Endo180 expressed on pancreatic stellate cells was found to be associated with local invasion mechanism as a leading cell of tumor-promoting pancreatic stellate cells. Furthermore, we identified autophagy was involved in the activation of pancreatic stellate cells. In the mouse model, suppression of autophagy of pancreatic stellate cells reduced tumor development and metastasis. From these results, we clarified the possibility of a new treatment strategy by reprogramming cancer microenvironment.
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Report
(4 results)
Research Products
(13 results)
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[Journal Article] Pancreatic stellate cells reorganize matrix components and lead pancreatic cancer invasion via the function of Endo1802018
Author(s)
Koikawa K, Ohuchida K, Takesue S, Ando Y, Kibe S, Nakayama H, Endo S, Abe T, Okumura T, Horioka K, Sada M, Iwamoto C, Moriyama T, Nakata K, Miyasaka Y, Ohuchida R, Manabe T, Ohtsuka T, Nagai E, Mizumoto K, Hashizume M, Nakamura M.
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Journal Title
Cancer Letters
Volume: 412
Pages: 143-154
DOI
Related Report
Peer Reviewed / Open Access
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[Journal Article] (The) Calpain inhibitor calpeptin suppresses pancreatic cancer by disrupting cancer-stromal interactions in a mouse xenograft model2016
Author(s)
Yoshida M, Miyasaka Y, Ohuchida Kenoki, Okumura T, Zheng B, Torata N, Fujita H, Nabae T, Manabe T, Shimamoto M, Ohtsuka T, Mizumoto K, Nakamura M
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Journal Title
Cancer Sci
Volume: 107
Issue: 10
Pages: 1443-1452
DOI
Related Report
Peer Reviewed / Open Access / Int'l Joint Research / Acknowledgement Compliant
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[Journal Article] Suppression of CD51 in pancreatic stellate cells inhibits tumor growth by reducing stroma and altering tumor-stromal interaction in pancreatic cancer2016
Author(s)
Horioka K, Ohuchida K, Sada M, Zheng B, Moriyama T, Fujita H, Manabe T, Ohtsuka T, Shimamoto M, Miyazaki T, Mizumoto K, Oda Y, Nakamura M.
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Journal Title
Int J Oncol
Volume: 48
Issue: 4
Pages: 1499-1508
DOI
Related Report
Peer Reviewed / Open Access / Int'l Joint Research
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[Journal Article] CD146 attenuation in cancer-associated fibroblasts promotes pancreatic cancer progression.2015
Author(s)
Zheng B, ohuchida K, Chijiiwa Y, Zhao M, Mizuuchi Y, Cui L, Horioka K, Ohtsuka T, Mizumoto K, Oda Y, Hashizume M, Nakamura M, Tanaka M
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Journal Title
Mol Carcinog
Volume: -
Issue: 11
Pages: 1560-1572
DOI
Related Report
Peer Reviewed / Open Access / Int'l Joint Research / Acknowledgement Compliant
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[Presentation] Pancreatic Stellate Cells Lead and Promote the Local Invasion of Cancer Cells, by Physically Remodeling the Extracellular Matrix with Collagen Fiber Alignment in Pancreatic Cancer2015
Author(s)
Koikawa K, Ohuchida K, Sada M, Abe T, Endo S, Horioka K, Moriyama T, Miyasaka Y, Ohtsuka T, Ohuchida R, Ueki T, Nagai E, Mizumoto K, Nakamura M
Organizer
American Pancreatic Association 46th Annual Meeting
Place of Presentation
San Diego(USA)
Year and Date
2015-11-04
Related Report
Int'l Joint Research
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