| Literature DB >> 29076001 |
Alessandra Santangelo1, Pietro Imbrucè2, Beatrice Gardenghi2, Laura Belli3, Rina Agushi2, Anna Tamanini1, Silvia Munari1, Alessandra Maria Bossi4, Ilaria Scambi2, Donatella Benati2, Raffaella Mariotti2, Gianfranco Di Gennaro1, Andrea Sbarbati2, Albino Eccher5, Giuseppe Kenneth Ricciardi6, Elisa Maria Ciceri6, Francesco Sala2, Giampietro Pinna3, Giuseppe Lippi1,2, Giulio Cabrini1,2, Maria Cristina Dechecchi7,8.
Abstract
Malignant gliomas, the most frequent primary brain tumors, are characterized by a dismal prognosis. Reliable biomarkers complementary to neuroradiology in the differential diagnosis of gliomas and monitoring for post-surgical progression are unmet needs. Altered expression of several microRNAs in tumour tissues from patients with gliomas compared to normal brain tissue have been described, thus supporting the rationale of using microRNA-based biomarkers. Although different circulating microRNAs were proposed in association with gliomas, they have not been introduced into clinical practice so far. Blood samples were collected from patients with high and low grade gliomas, both before and after surgical resection, and the expression of miR-21, miR-222 and miR-124-3p was measured in exosomes isolated from serum. The expression levels of miR-21, miR-222 and miR-124-3p in serum exosomes of patients with high grade gliomas were significantly higher than those of low grade gliomas and healthy controls and were sharply decreased in samples obtained after surgery. The analysis of miR-21, miR-222 and miR-124-3p in serum exosomes of patients affected by gliomas can provide a minimally invasive and innovative tool to help the differential diagnosis of gliomas at their onset in the brain and predict glioma grading and non glial metastases before surgery.Entities:
Keywords: Circulating biomarkers; Exosomes; Gliomas; MiRNAs
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Year: 2017 PMID: 29076001 DOI: 10.1007/s11060-017-2639-x
Source DB: PubMed Journal: J Neurooncol ISSN: 0167-594X Impact factor: 4.130