Prognostic value of Musashi-1 in gliomas

被引:50
|
作者
Dahlrot, Rikke H. [1 ,2 ]
Hansen, Steinbjorn [1 ,2 ]
Herrstedt, Jorn [1 ,2 ]
Schroder, Henrik D. [2 ,3 ]
Hjelmborg, Jacob [4 ]
Kristensen, Bjarne W. [2 ,3 ]
机构
[1] Odense Univ Hosp, Dept Oncol, DK-5000 Odense, Denmark
[2] Univ Southern Denmark, Inst Clin Res, Odense, Denmark
[3] Odense Univ Hosp, Dept Pathol, DK-5000 Odense, Denmark
[4] Univ Southern Denmark, Inst Publ Hlth, Dept Biostat, Odense, Denmark
基金
英国医学研究理事会;
关键词
Glioma; Glioblastoma; Prognosis; Stem cell; Musashi-1; MSI1; protein; RNA-BINDING PROTEIN; AUTOMATED QUANTITATIVE-ANALYSIS; CANCER STEM-CELLS; GRADE GLIOMAS; ANALYSIS AQUA; EXPRESSION; IDENTIFICATION; MARKER; QUANTIFICATION; LOCALIZATION;
D O I
10.1007/s11060-013-1246-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The aim of this study was to investigate the prognostic value of the RNA-binding protein Musashi-1 in adult patients with primary gliomas. Musashi-1 has been suggested to be a cancer stem cell-related marker in gliomas, and high levels of Musashi-1 have been associated with high tumor grades and hence poor prognosis. Samples of 241 gliomas diagnosed between 2005 and 2009 were stained with an anti-Musashi-1 antibody using a fluorescent staining protocol followed by automated image acquisition and processing. Musashi-1 area fraction and intensity in cytoplasm and in nuclei were quantified by systematic random sampling in 2 % of the vital tumor area. In WHO grade III tumors high levels of Musashi-1 were associated with poor survival in multivariate analysis (HR 3.39, p = 0.02). We identified a sub-population of glioblastoma (GBM) patients with high levels of Musashi-1 and a superior prognosis (HR 0.65, p = 0.038). In addition patients with high levels of Musashi-1 benefitted most from post-surgical treatment, indicating that Musashi-1 may be a predictive marker in GBMs. In conclusion, our results suggest that high levels of Musashi-1 are associated with poor survival in patients with WHO grade III tumors and that Musashi-1 may be a predictive marker in GBMs, although further validation is needed. We find the combination of immunofluorescence and automated quantitation to be a feasible, robust, and reproducible approach for quantitative biomarker studies.
引用
收藏
页码:453 / 461
页数:9
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