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RETRACTED: Dysregulation of Survivin-Targeting microRNAs in Autoimmune Diseases: New Perspectives for Novel Therapies

Navid ShomaliDepartment of Immunology, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, IranMarwah Suliman MaashiMedical Laboratory Technology Department, Faculty of Applied Medical Sciences, King Abdulaziz University, Jeddah, Saudi ArabiaBehzad BaradaranDepartment of Immunology, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, IranAmin Daei SorkhabiStudent Research Committee, Tabriz University of Medical Sciences, Tabriz, IranAila SarkeshStudent Research Committee, Tabriz University of Medical Sciences, Tabriz, IranHamed MohammadiDepartment of Immunology, School of Medicine, Alborz University of Medical Sciences, Karaj, IranMaryam HemmatzadehDepartment of Immunology, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, IranFaroogh MarofiImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, IranSiamak Sandoghchian ShotorbaniDepartment of Immunology, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, IranMostafa JarahianGerman Cancer Research Center, Toxicology and Chemotherapy Unit (G401), Heidelberg, Germany
2022en
ABI

Аннотация

It has been well established that the etiopathogenesis of diverse autoimmune diseases is rooted in the autoreactive immune cells’ excessively proliferative state and impaired apoptotic machinery. Survivin is an anti-apoptotic and mitotic factor that has sparked a considerable research interest in this field. Survivin overexpression has been shown to contribute significantly to the development of autoimmune diseases via autoreactive immune cell overproliferation and apoptotic dysregulation. Several microRNAs (miRNAs/miRs) have been discovered to be involved in survivin regulation, rendering the survivin-miRNA axis a perspective target for autoimmune disease therapy. In this review, we discuss the role of survivin as an immune regulator and a highly implicated protein in the pathogenesis of autoimmune diseases, the significance of survivin-targeting miRNAs in autoimmunity, and the feasibility of targeting the survivin-miRNA axis as a promising therapeutic option for autoimmune diseases.

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