Identification of novel diagnostic markers for early detection of pancreatic cancer; application for a low-invasive fluid test
| Project/Area Number |
26293285
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| Research Category |
Grant-in-Aid for Scientific Research (B)
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| Allocation Type | Partial Multi-year Fund |
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| Section | 一般 |
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| Research Field |
General surgery
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| Research Institution | Nagoya University |
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Principal Investigator |
KODERA Yasuhiro 名古屋大学, 医学(系)研究科(研究院), 教授 (10345879)
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| Co-Investigator(Kenkyū-buntansha) |
神田 光郎 名古屋大学, 医学部附属病院, 助教 (00644668)
山田 豪 名古屋大学, 医学部附属病院, 病院講師 (30467287)
藤井 努 名古屋大学, 医学(系)研究科(研究院), 准教授 (60566967)
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| Project Period (FY) |
2014-04-01 – 2017-03-31
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| Project Status |
Completed (Fiscal Year 2016)
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| Budget Amount *help |
¥16,250,000 (Direct Cost: ¥12,500,000、Indirect Cost: ¥3,750,000)
Fiscal Year 2016: ¥4,160,000 (Direct Cost: ¥3,200,000、Indirect Cost: ¥960,000)
Fiscal Year 2015: ¥5,460,000 (Direct Cost: ¥4,200,000、Indirect Cost: ¥1,260,000)
Fiscal Year 2014: ¥6,630,000 (Direct Cost: ¥5,100,000、Indirect Cost: ¥1,530,000)
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| Keywords | 低侵襲スクリーニング法 / 膵腫瘍 / 次世代シーケンサー / 低侵襲スクリーング法 / 氏世代シーケンサー |
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| Outline of Final Research Achievements |
Previous studies indicated that pancreatic and duodenal juice samples are an excellent source of mutant DNA from the pancreas and have the potential to help in the risk stratification and surveillance of patients undergoing pancreatic screening. To identify novel genetic alterations specific to high grade precursors, we conducted an exome sequencing analysis. Mutations at NOTCH2, AFF3, EXT1, IL21R and CDH6 were frequently found in the high grade pancreatic intraepithelial neoplasias and ductal adenocarcinoma, but not normal ducts, indicating that these are promising markers for early detection of pancreatic cancer. We employed two highly-sensitive methods, Cast PCR and digital HRM, to detect less abundance of mutation and successfully detect 0.1% of mutant alleles. One or more of NOTCH2, AFF3, EXT1, IL21R and CDH6 mutations were found in the cystic fluids from high grade intraductal papillary mucinous neoplasms (IPMNs), whereas no mutations were seen in those from low grade IPMNs.
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Report
(4 results)
Research Products
(2 results)
