Non‐m6A RNA modifications in haematological malignancies

Author:

Chen Meiling12,Chen Yuanzhong1,Wang Kitty2,Deng Xiaolan2,Chen Jianjun23ORCID

Affiliation:

1. Department of Hematology Fujian Institute of Hematology Fujian Provincial Key Laboratory on Hematology Fujian Medical University Union Hospital Fuzhou China

2. Department of Systems Biology Beckman Research Institute of City of Hope Monrovia California USA

3. Gehr Family Center for Leukemia Research City of Hope Medical Center and Comprehensive Cancer Center Duarte California USA

Abstract

AbstractDysregulated RNA modifications, stemming from the aberrant expression and/or malfunction of RNA modification regulators operating through various pathways, play pivotal roles in driving the progression of haematological malignancies. Among RNA modifications, N6‐methyladenosine (m6A) RNA modification, the most abundant internal mRNA modification, stands out as the most extensively studied modification. This prominence underscores the crucial role of the layer of epitranscriptomic regulation in controlling haematopoietic cell fate and therefore the development of haematological malignancies. Additionally, other RNA modifications (non‐m6A RNA modifications) have gained increasing attention for their essential roles in haematological malignancies. Although the roles of the m6A modification machinery in haematopoietic malignancies have been well reviewed thus far, such reviews are lacking for non‐m6A RNA modifications. In this review, we mainly focus on the roles and implications of non‐m6A RNA modifications, including N4‐acetylcytidine, pseudouridylation, 5‐methylcytosine, adenosine to inosine editing, 2′‐O‐methylation, N1‐methyladenosine and N7‐methylguanosine in haematopoietic malignancies. We summarise the regulatory enzymes and cellular functions of non‐m6A RNA modifications, followed by the discussions of the recent studies on the biological roles and underlying mechanisms of non‐m6A RNA modifications in haematological malignancies. We also highlight the potential of therapeutically targeting dysregulated non‐m6A modifiers in blood cancer.

Funder

National Institutes of Health

Publisher

Wiley

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