The Regulation of m6A Modification in Glioblastoma: Functional Mechanisms and Therapeutic Approaches

Author:

Deacon Simon12,Walker Lauryn1,Radhi Masar1,Smith Stuart12ORCID

Affiliation:

1. Children’s Brain Tumour Research Centre, University of Nottingham, Nottingham NG7 2RD, UK

2. Nottingham University Hospitals NHS Trust, Nottingham NG7 2UH, UK

Abstract

Glioblastoma is the most prevalent primary brain tumour and invariably confers a poor prognosis. The immense intra-tumoral heterogeneity of glioblastoma and its ability to rapidly develop treatment resistance are key barriers to successful therapy. As such, there is an urgent need for the greater understanding of the tumour biology in order to guide the development of novel therapeutics in this field. N6-methyladenosine (m6A) is the most abundant of the RNA modifications in eukaryotes. Studies have demonstrated that the regulation of this RNA modification is altered in glioblastoma and may serve to regulate diverse mechanisms including glioma stem-cell self-renewal, tumorigenesis, invasion and treatment evasion. However, the precise mechanisms by which m6A modifications exert their functional effects are poorly understood. This review summarises the evidence for the disordered regulation of m6A in glioblastoma and discusses the downstream functional effects of m6A modification on RNA fate. The wide-ranging biological consequences of m6A modification raises the hope that novel cancer therapies can be targeted against this mechanism.

Funder

NIHR Academic Clinical Fellowship

the Jean-Shanks Foundation

the Pathological Society of Great Britain and Ireland

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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