Project/Area Number |
24592128
|
Research Category |
Grant-in-Aid for Scientific Research (C)
|
Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Cerebral neurosurgery
|
Research Institution | Okayama University |
Principal Investigator |
SUGIU Kenji 岡山大学, 大学病院, 准教授 (40325105)
|
Co-Investigator(Kenkyū-buntansha) |
KUROZUMI Kazuhiko 岡山大学, 大学病院, 講師 (20509608)
|
Co-Investigator(Renkei-kenkyūsha) |
DATE Isao 岡山大学, 医歯薬学総合研究科, 教授 (70236785)
|
Project Period (FY) |
2012-04-01 – 2015-03-31
|
Project Status |
Completed (Fiscal Year 2014)
|
Budget Amount *help |
¥5,330,000 (Direct Cost: ¥4,100,000、Indirect Cost: ¥1,230,000)
Fiscal Year 2014: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Fiscal Year 2013: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2012: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
|
Keywords | 分子標的薬 / バイオマーカー / インテグリン / グリオーマ / cilengitide / CYR61 / Cilengitide |
Outline of Final Research Achievements |
Recently,research efforts in identifying prognostic molecular biomarkers for malignant glioma have intensified. Cysteine-rich protein 61(CYR61)is one of the CCN family of matricellular proteins that promotes cell growth and angiogenesis in cancers through its interaction with several integrins. In this study,we investigated the relationships among CYR61,O6-methylguanine-DNA methyltransferase(MGMT)expression,the tumor removal rate and prognosis in 46 glioblastoma patients treated at the Okayama University Hospital. CYR61 expression was positive in 31(67%)of these patients. The median progression-free survival(PFS)and overall survival(OS)times of patients with strong CYR61 expression was significantly shorter than those of patients with weak CYR61 expression. In a multivariate Cox analysis,CYR61 proved to be an independent prognostic factor for patient survival. It was concluded that CYR61 might emerge as a significant prognostic factor regarding the prognosis of glioblastoma patients.
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