Development of novel therapies that focus on specific stroma cell induced peritoneal dissemination of pancreatic cancer
Project/Area Number |
25861198
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Multi-year Fund |
Research Field |
Digestive surgery
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Research Institution | Kyushu University |
Principal Investigator |
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Project Period (FY) |
2013-04-01 – 2015-03-31
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Project Status |
Completed (Fiscal Year 2014)
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Budget Amount *help |
¥4,030,000 (Direct Cost: ¥3,100,000、Indirect Cost: ¥930,000)
Fiscal Year 2014: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Fiscal Year 2013: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
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Keywords | 膵癌 / 筋線維芽細胞 / 腹膜播種 / 癌間質相互作用 / 腹膜中皮細胞 / 線維芽細胞 |
Outline of Final Research Achievements |
This study was designed to assess the role of myofibroblasts at peritoneally disseminated sites of pancreatic cancer. Human peritoneal myofibroblasts (hPMFs) were established from disseminated sites of pancreatic cancer and their interactions with the SUIT-2 and CAPAN-1 human pancreatic cancer cell lines were analyzed in vitro and in vivo. In vitro, hPMFs significantly promoted the migration and invasion of pancreatic cancer cells (P<0.05), while the cancer cells significantly promoted the migration and invasion of hPMFs (P<0.05). In vivo, the number of perito-neally disseminated nodules was significantly greater in mice implanted with cancer cells plus hPMFs compared to mice implanted with cancer cells alone. HPMFs promote the peritoneal dissemination of pancreatic cancer. The cancer-stromal cell interaction in the peritoneal cavity may be a new therapeutic target to prevent the dissemination of pancreatic cancer.
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Report
(3 results)
Research Products
(3 results)
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[Journal Article] Peritoneal myofibroblasts at metastatic foci promote dissemination of pancreatic cancer.2014
Author(s)
Akagawa S, Ohuchida K, Torata N, Hattori M, Eguchi D, Fujiwara K, Kozono S, Cui L, Ikenaga N, Ohtsuka T, Oishima S, Mizumoto K, Oda Y, Tanaka M
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Journal Title
Int J Oncol
Volume: 45
Issue: 1
Pages: 113-120
DOI
Related Report
Peer Reviewed / Acknowledgement Compliant
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