Micro RNAs as a Diagnostic Marker between Glioma and Primary CNS Lymphoma: A Systematic Review

Author:

Dabbagh Ohadi Mohammad Amin12,Aleyasin Mir Sajjad3,Samiee Reza3ORCID,Bordbar Sanaz3,Maroufi Seyed Farzad1,Bayan Nikoo3,Hanaei Sara4ORCID,Smith Timothy R.5

Affiliation:

1. Department of Pediatric Neurological Surgery, Children’s Medical Center, Tehran University of Medical Sciences, Tehran 1419733151, Iran

2. Interdisciplinary Neuroscience Research Program, Tehran University of Medical Sciences, Tehran 1417755331, Iran

3. Students’ Scientific Research Center, Tehran University of Medical Sciences, Tehran 1417755331, Iran

4. Neurosurgery Department, Imam Khomeini Hospital Complex (IKHC), Tehran University of Medical Sciences, Tehran 1419733151, Iran

5. Department of Neurosurgery, Brigham and Women’s Hospital, Boston, MA 02115, USA

Abstract

Differentiating glioma from primary central nervous system lymphoma (PCNSL) can be challenging, and current diagnostic measures such as MRI and biopsy are of limited efficacy. Liquid biopsies, which detect circulating biomarkers such as microRNAs (miRs), may provide valuable insights into diagnostic biomarkers for improved discrimination. This review aimed to investigate the role of specific miRs in diagnosing and differentiating glioma from PCNSL. A systematic search was conducted of PubMed, Scopus, Web of Science, and Embase for articles on liquid biopsies as a diagnostic method for glioma and PCNSL. Sixteen dysregulated miRs were identified with significantly different levels in glioma and PCNSL, including miR-21, which was the most prominent miR with higher levels in PCNSL, followed by glioma, including glioblastoma (GBM), and control groups. The lowest levels of miR-16 and miR-205 were observed in glioma, followed by PCNSL and control groups, whereas miR-15b and miR-301 were higher in both tumor groups, with the highest levels observed in glioma patients. The levels of miR-711 were higher in glioma (including GBM) and downregulated in PCNSL compared to the control group. This review suggests that using these six circulating microRNAs as liquid biomarkers with unique changing patterns could aid in better discrimination between glioma, especially GBM, and PCNSL.

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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