Challenges in proteomics-based biomarker discovery of refractory and advanced neuroblastoma
| Project/Area Number |
15K20299
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| Research Category |
Grant-in-Aid for Young Scientists (B)
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| Allocation Type | Multi-year Fund |
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| Research Field |
Pediatric surgery
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| Research Institution | Mie University |
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Principal Investigator |
OTAKE Kohei 三重大学, 医学部, 助教 (40378344)
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| Project Period (FY) |
2015-04-01 – 2017-03-31
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| Project Status |
Completed (Fiscal Year 2016)
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| Budget Amount *help |
¥3,770,000 (Direct Cost: ¥2,900,000、Indirect Cost: ¥870,000)
Fiscal Year 2016: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2015: ¥2,600,000 (Direct Cost: ¥2,000,000、Indirect Cost: ¥600,000)
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| Keywords | 神経芽腫 / マーカー / 予後因子 / プロテオミクス / DDX39A |
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| Outline of Final Research Achievements |
Shotgun proteomic analysis was performed in undifferentiated and ATRA-induced differentiated NB cells in vitro. An identified protein was verified by MRM and western blot analysis. Immunohistochemistry (IHC) was used to examine the expression of the identified protein in 33 primary NB tissues. Twelve proteins, including ATP-dependent RNA helicase (DDX39A), were only detected in undifferentiated NB cells. A peptide of DDX39A was detected at a significantly higher level in undifferentiated IMR-32 and LA-N-1 cells by MRM. Western blot analysis revealed that DDX39A expression was significantly higher in undifferentiated IMR-32 and LA-N-1 cells. IHC demonstrated that DDX39A was highly expressed in the primary tumor tissues of patients with poor prognosis, and univariate and multivariate survival analyzes showed that DDX39A expression could be an independent unfavorable prognostic factor. DDX39A is a potential biomarker for unfavorable NB using a proteomic approach.
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Report
(3 results)
Research Products
(4 results)
