A differentially expressed set of microRNAs in cerebro-spinal fluid (CSF) can diagnose CNS malignancies

被引:85
作者
Drusco, Alessandra [1 ]
Bottoni, Arianna [1 ]
Lagana', Alessandro [2 ]
Acunzo, Mario [1 ]
Fassan, Matteo [3 ]
Cascione, Luciano [5 ,6 ]
Antenucci, Anna [4 ]
Kumchala, Prasanthi [1 ]
Vicentini, Caterina [7 ]
Gardiman, Marina P. [3 ]
Alder, Hansjuerg [1 ]
Carosi, Mariantonia A. [8 ]
Ammirati, Mario [9 ]
Gherardi, Stefano [10 ]
Luscri', Marilena [10 ]
Carapella, Carmine [11 ]
Zanesi, Nicola [1 ]
Croce, Carlo M. [1 ]
机构
[1] Ohio State Univ, MVIMG, Columbus, OH 43210 USA
[2] Icahn Sch Med Mt Sinai, Dept Genet & Genom Sci, New York, NY 10029 USA
[3] Univ Padua, Surg Pathol & Cytopathol Unit, Dept Med DIMED, Padua, Italy
[4] Regina Elena Inst Canc Res, UOSD Clin Pathol, Rome, Italy
[5] IOR, Lymphoma & Genom Res Program, Bellinzona, Switzerland
[6] IOSI Oncol Inst Southern Switzerland, Bellinzona, Switzerland
[7] Univ & Hosp Trust Verona, ARC NET Res Ctr, Verona, Italy
[8] Regina Elena Inst Canc Res, Dept Pathol, Rome, Italy
[9] Ohio State Univ, Dept Neurol Surg, Columbus, OH 43210 USA
[10] Sandro Pertini Hosp, Dept Anesthesiol, Rome, Italy
[11] Regina Elena Inst Canc Res, Dept Neurol Surg, Rome, Italy
关键词
microRNA; cerebro-spinal fluid (CSF); brain tumors; biomarkers; MIR-125B; BRAIN; PROLIFERATION; BIOMARKERS; SIGNATURES; PRECURSOR; PROMOTES; GROWTH; TUMORS; CELLS;
D O I
10.18632/oncotarget.4096
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Central Nervous System malignancies often require stereotactic biopsy or biopsy for differential diagnosis, and for tumor staging and grading. Furthermore, stereotactic biopsy can be non-diagnostic or underestimate grading. Hence, there is a compelling need of new diagnostic biomarkers to avoid such invasive procedures. Several biological markers have been proposed, but they can only identify specific prognostic subtype of Central Nervous System tumors, and none of them has found a standardized clinical application. The aim of the study was to identify a Cerebro-Spinal Fluid microRNA signature that could differentiate among Central Nervous System malignancies. CSF total RNA of 34 neoplastic and of 14 non-diseased patients was processed by NanoString. Comparison among groups (Normal, Benign, Glioblastoma, Medulloblastoma, Metastasis and Lymphoma) lead to the identification of a microRNA profile that was further confirmed by RT-PCR and in situ hybridization. Hsa-miR-451, -711, 935, -223 and -125b were significantly differentially expressed among the above mentioned groups, allowing us to draw an hypothetical diagnostic chart for Central Nervous System malignancies. This is the first study to employ the NanoString technique for Cerebro-Spinal Fluid microRNA profiling. In this article, we demonstrated that Cerebro-Spinal Fluid microRNA profiling mirrors Central Nervous System physiologic or pathologic conditions. Although more cases need to be tested, we identified a diagnostic Cerebro-Spinal Fluid microRNA signature with good perspectives for future diagnostic clinical applications.
引用
收藏
页码:20829 / 20839
页数:11
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