Clinical Relevance and Interplay between miRNAs in Influencing Glioblastoma Multiforme Prognosis

Author:

Epistolio Samantha1ORCID,Dazio Giulia1,Zaed Ismail2,Sahnane Nora3,Cipriani Debora2,Polinelli Francesco2ORCID,Barizzi Jessica1,Spina Paolo1ORCID,Stefanini Federico Mattia4ORCID,Cerati Michele3,Balbi Sergio5,Mazzucchelli Luca16,Sessa Fausto3,Pesce Gianfranco Angelo7,Reinert Michael28ORCID,Cardia Andrea2ORCID,Marchi Francesco2ORCID,Frattini Milo1

Affiliation:

1. Laboratory of Genetics and Molecular Pathology, Institute of Pathology, Ente Ospedaliero Cantonale (EOC), 6900 Locarno, Switzerland

2. Service of Neurosurgery, Neurocenter of the Southern Switzerland, Regional Hospital of Lugano, Ente Ospedaliero Cantonale (EOC), 6900 Lugano, Switzerland

3. Unit of Pathology, Department of Medicine and Technological Innovation, University of Insubria, ASST Sette Laghi, 21100 Varese, Italy

4. Department of Environmental Science and Policy, Faculty of Science and Technology-ESP, University of Milan, 20122 Milan, Italy

5. Division of Neurological Surgery, Department of Biotechnology and Life Sciences, University of Insubria, ASST Sette Laghi, 21100 Varese, Italy

6. Faculty of Biomedical Sciences, Università della Svizzera italiana, 6900 Lugano, Switzerland

7. Radiation Oncology, Oncology Institute of Southern Switzerland, Ente Ospedaliero Cantonale (EOC), 6501 Bellinzona, Switzerland

8. Faculty of Medicine, University of the Southern Switzerland, 6900 Lugano, Switzerland

Abstract

Glioblastoma multiforme (GBM) is usually treated with surgery followed by adjuvant partial radiotherapy combined with temozolomide (TMZ) chemotherapy. Recent studies demonstrated a better survival and good response to TMZ in methylguanine-DNA methyltransferase (MGMT)-methylated GBM cases. However, approximately 20% of patients with MGMT-unmethylated GBM display an unexpectedly favorable outcome. Therefore, additional mechanisms related to the TMZ response need to be investigated. As such, we decided to investigate the clinical relevance of six miRNAs involved in brain tumorigenesis (miR-181c, miR-181d, miR-21, miR-195, miR-196b, miR-648) as additional markers of response and survival in patients receiving TMZ for GBM. We evaluated miRNA expression and the interplay between miRNAs in 112 IDH wt GBMs by applying commercial assays. Then, we correlated the miRNA expression with patients’ clinical outcomes. Upon bivariate analyses, we found a significant association between the expression levels of the miRNAs analyzed, but, more interestingly, the OS curves show that the combination of low miR-648 and miR-181c or miR-181d expressions is associated with a worse prognosis than cases with other low-expression miRNA pairs. To conclude, we found how specific miRNA pairs can influence survival in GBM cases treated with TMZ.

Funder

Fondazione Ticinese contro il Cancro

Publisher

MDPI AG

Subject

General Medicine

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