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Long non-coding RNAs in schizophrenia: Genetic variations, treatment markers and potential targeted signaling pathways. | LitMetric

Long non-coding RNAs in schizophrenia: Genetic variations, treatment markers and potential targeted signaling pathways.

Schizophr Res

Department of Pharmacy, Second Xiangya Hospital, Central South University, Changsha, Hunan, China; Institute of Clinical Pharmacy, Second Xiangya Hospital, Central South University, Changsha, Hunan, China. Electronic address:

Published: October 2023

AI Article Synopsis

  • Schizophrenia (SZ) is a complex psychiatric disorder influenced by a mix of genetic and environmental factors, with long non-coding RNAs (lncRNAs) emerging as key players in understanding its mechanisms.
  • About 30-40% of lncRNAs are highly expressed in the brain regions related to SZ, and their regulation may be significant in how atypical antipsychotic drugs (AAPDs) function.
  • This review highlights the dysregulation of lncRNAs, their genetic variations, and their potential roles in the pathology of SZ, suggesting they could be valuable therapeutic targets for treatment.

Article Abstract

Schizophrenia (SZ), a complex and debilitating spectrum of psychiatric disorders, is now mainly attributed to multifactorial etiology that includes genetic and environmental factors. Long non-coding RNAs (lncRNAs) are gaining popularity as a way to better understand the comprehensive mechanisms beneath the clinical manifestation of SZ. Only in recent years has it been elucidated that mammalian genomes encode thousands of lncRNAs. Strikingly, roughly 30-40% of these lncRNAs are extensively expressed in different regions across the brain, which may be closely associated with SZ. The therapeutic and adverse effects of atypical antipsychotic drugs (AAPDs) are partially reflected by their role in the regulation of lncRNAs. This begs the question directly, do any lncRNAs exist as biomarkers for AAPDs treatment? Furthermore, we comprehend a range of mechanistic investigations that have revealed the regulatory roles for lncRNAs both involved in the brain and the periphery of SZ. More crucially, we also combine insights from a variety of signaling pathways to argue that lncRNAs probably play critical roles in SZ via their interactive downstream factors. This review provides a thorough understanding regarding dysregulation of lncRNAs, corresponding genetic alternations, as well as their potential regulatory roles in the pathology of SZ, which might help reveal useful therapeutic targets in SZ.

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Source
http://dx.doi.org/10.1016/j.schres.2023.07.027DOI Listing

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