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The curious case of miR-155 in SLE

Published online by Cambridge University Press:  01 September 2021

S. A. Ibrahim
Affiliation:
School of Medicine, NewGiza University (NGU), Giza, Egypt
A. Y. Afify
Affiliation:
School of Medicine, NewGiza University (NGU), Giza, Egypt
I. O. Fawzy
Affiliation:
School of Medicine, NewGiza University (NGU), Giza, Egypt
N. El-Ekiaby
Affiliation:
School of Medicine, NewGiza University (NGU), Giza, Egypt
A. I. Abdelaziz*
Affiliation:
School of Medicine, NewGiza University (NGU), Giza, Egypt
*
Author for correspondence: A. I. Abdelaziz, E-mail: [email protected]

Abstract

Epigenetic modifications have been well documented in autoimmune diseases. MicroRNAs (miRNAs), in particular, have long intrigued scientists in the field of autoimmunity. Owing to its central role in the development of the immune system, microRNA-155 (miR-155) is deeply involved in systemic lupus erythematosus (SLE). Despite the advancements made in treating SLE, the disease still remains incurable. Therefore, recent attention has been drawn to the manipulation of epigenetics in the development of curative treatments. In fact, it is a widely held view that miRNA-targeted therapy is a new glimmer of hope in the treatment of autoimmune diseases. However, the duplicity of miRNAs should not be overlooked. A single miRNA can target several mRNAs, and some mRNAs may possess opposing functions. In this review, we highlight the role of miR-155 as a biomarker and review its functions in SLE patients and animal models while discussing possible reasons behind inconsistencies across studies.

Type
Review
Copyright
Copyright © The Author(s), 2021. Published by Cambridge University Press

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