| Project/Area Number |
26461995
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Multi-year Fund |
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| Section | 一般 |
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| Research Field |
Digestive surgery
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| Research Institution | Iwate Medical University |
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Principal Investigator |
Akiyama Yuji 岩手医科大学, 医学部, 講師 (10405798)
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| Co-Investigator(Kenkyū-buntansha) |
岩谷 岳 岩手医科大学, 医学部, 講師 (70405801)
西塚 哲 岩手医科大学, 医学部, 教授 (50453311)
若林 剛 岩手医科大学, 医学部, 教授 (50175064)
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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 |
¥4,940,000 (Direct Cost: ¥3,800,000、Indirect Cost: ¥1,140,000)
Fiscal Year 2016: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2015: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2014: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
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| Keywords | 食道癌 / 癌抑制遺伝子 / 膜結合型セリンプロテアーゼ / TMPRSS11B / 膜型セリンプロテアーゼ / TMPRSS11 / （１） 食道癌 / 遺伝子発現 |
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| Outline of Final Research Achievements |
This study aims to identify the genes responsible for esophageal squamous cell carcinoma (ESCC) development, using gene expression profiling. Our transcriptome sequence analysis of surgically resected tumors and the corresponding normal tissues from 3 patients with ESCC revealed that transmembrane protease serine 11 (TMPRSS11) subfamily genes showed decreased expression in ESCC tissues. A quantitative reverse transcription PCR demonstrated a downregulation of TMPRSS11B in ESCC tissues, compared with its expression in the corresponding normal tissues (n = 64, p < 0.0001 ). There was no significant difference in the clinico-pathological factors between TMPRSS11B - high and TMPRSS11B -low expression groups. Moreover, TMPRSS11B expression was not detected in any of the 10 ESCC cell lines investigated, and overexpression of TMPRSS11B induced downregulation of EGFR and Akt in the ESCC cell line KYSE410. Our results suggest that TMPRSS11B has tumor suppressive roles in ESCC.
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