Development of the new squamous cell carcinoma marker that applied TGFbeta-associated extracellular secretion protein
Project/Area Number |
25861926
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Multi-year Fund |
Research Field |
Surgical dentistry
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Research Institution | Nagoya 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 |
¥3,640,000 (Direct Cost: ¥2,800,000、Indirect Cost: ¥840,000)
Fiscal Year 2014: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2013: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
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Keywords | CD109 / 口腔扁平上皮癌 / 血液腫瘍マーカー / TGFβシグナル / TGFbetaシグナル |
Outline of Final Research Achievements |
In xenografted BALB/c-nu/nu mice that were subcutaneously injected the FLAG-tagged CD109 overexpressing cells, CD109 secreted from inoculated tumors was detected in sera, using western blotting and CD109 ELISA. Concentrations of tumor-secreted CD109 increased proportionally as tumors enlarged. These results indicate that CD109 is present in serum as a soluble form, and suggest its potential as a novel tumor marker in patients with cancers that express CD109. In clinical experiment, concentration of CD109 in sera that were from oral cancer patients including precancerous lesion was measured using CD109 ELISA. The result did not reflect the tumor size dependent manner that was shown in xenografted mice.
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Report
(3 results)
Research Products
(4 results)
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[Journal Article] CD109 attenuates TGF-β1 signaling and enhances EGF signaling in SK-MG-1 human glioblastoma cells.2015
Author(s)
Jing-Min Zhang, Yoshiki Murakumo, Sumitaka Hagiwara, Ping Jiang, Shinji Mii, Emir Kalyoncu, Shoji Saito, Chikage Suzuki, Yasutaka Sakurai, Yoshiko Numata, Toshimichi Yamamoto, Masahide Takahashi
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Journal Title
Biochemical and Biophysical Research Communications
Volume: 459
Issue: 2
Pages: 252-258
DOI
Related Report
Peer Reviewed / Open Access / Acknowledgement Compliant
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