» Articles » PMID: 34421622

LncRNAs As Therapeutic Targets and Potential Biomarkers for Lipid-Related Diseases

Overview
Journal Front Pharmacol
Date 2021 Aug 23
PMID 34421622
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

Lipid metabolism is an essential biological process involved in nutrient adjustment, hormone regulation, and lipid homeostasis. An irregular lifestyle and long-term nutrient overload can cause lipid-related diseases, including atherosclerosis, myocardial infarction (MI), obesity, and fatty liver diseases. Thus, novel tools for efficient diagnosis and treatment of dysfunctional lipid metabolism are urgently required. Furthermore, it is known that lncRNAs based regulation like sponging microRNAs (miRNAs) or serving as a reservoir for microRNAs play an essential role in the progression of lipid-related diseases. Accordingly, a better understanding of the regulatory roles of lncRNAs in lipid-related diseases would provide the basis for identifying potential biomarkers and therapeutic targets for lipid-related diseases. This review highlighted the latest advances on the potential biomarkers of lncRNAs in lipid-related diseases and summarised current knowledge on dysregulated lncRNAs and their potential molecular mechanisms. We have also provided novel insights into the underlying mechanisms of lncRNAs which might serve as potential biomarkers and therapeutic targets for lipid-related diseases. The information presented here may be useful for designing future studies and advancing investigations of lncRNAs as biomarkers for diagnosis, prognosis, and therapy of lipid-related diseases.

Citing Articles

Importance of long non-coding RNAs in the pathogenesis, diagnosis, and treatment of myocardial infarction.

Zolfaghari Dehkharghani M, Mousavi S, Kianifard N, Fazlzadeh A, Parsa H, Tavakoli Pirzaman A Int J Cardiol Heart Vasc. 2024; 55:101529.

PMID: 39498345 PMC: 11532444. DOI: 10.1016/j.ijcha.2024.101529.


The Role of Selected lncRNAs in Lipid Metabolism and Cardiovascular Disease Risk.

Gluba-Sagr A, Franczyk B, Rysz-Gorzynska A, Olszewski R, Rysz J Int J Mol Sci. 2024; 25(17).

PMID: 39273193 PMC: 11395304. DOI: 10.3390/ijms25179244.


A Holistic Analysis of Alzheimer's Disease-Associated lncRNA Communities Reveals Enhanced lncRNA-miRNA-RBP Regulatory Triad Formation Within Functionally Segregated Clusters.

Sen S, Mukhopadhyay D J Mol Neurosci. 2024; 74(3):77.

PMID: 39143264 PMC: 11324768. DOI: 10.1007/s12031-024-02244-0.


Modulating the Expression of Exercise-induced lncRNAs: Implications for Cardiovascular Disease Progression.

Yu L, Zhang G J Cardiovasc Transl Res. 2024; .

PMID: 38858339 DOI: 10.1007/s12265-024-10530-w.


The long non-coding RNAs (lncRNA) in the pathogenesis of gastric cancer cells: molecular mechanisms and involvement miRNAs.

Saleh R, Al-Hawary S, Hammoud A, Hjazi A, Abdulrazzaq S, Rajput P Mol Biol Rep. 2024; 51(1):615.

PMID: 38704760 DOI: 10.1007/s11033-024-09546-x.


References
1.
Lan X, Wu L, Wu N, Chen Q, Li Y, Du X . Long Noncoding RNA lnc-HC Regulates PPARγ-Mediated Hepatic Lipid Metabolism through miR-130b-3p. Mol Ther Nucleic Acids. 2019; 18:954-965. PMC: 6881655. DOI: 10.1016/j.omtn.2019.10.018. View

2.
Pan X, Cheng R, Zhu X, Cai F, Zheng G, Li J . Prognostic Significance and Diagnostic Value of Overexpressed lncRNA PVT1 in Colorectal Cancer. Clin Lab. 2019; 65(12). DOI: 10.7754/Clin.Lab.2019.190412. View

3.
Spiroski A, Sanders R, Meloni M, McCracken I, Thomson A, Brittan M . The Influence of the LINC00961/SPAAR Locus Loss on Murine Development, Myocardial Dynamics, and Cardiac Response to Myocardial Infarction. Int J Mol Sci. 2021; 22(2). PMC: 7835744. DOI: 10.3390/ijms22020969. View

4.
Tontonoz P, Wu X, Jones M, Zhang Z, Salisbury D, Sallam T . Long Noncoding RNA Facilitated Gene Therapy Reduces Atherosclerosis in a Murine Model of Familial Hypercholesterolemia. Circulation. 2017; 136(8):776-778. PMC: 5657526. DOI: 10.1161/CIRCULATIONAHA.117.029002. View

5.
Zhang M, Chi X, Qu N, Wang C . Long noncoding RNA lncARSR promotes hepatic lipogenesis via Akt/SREBP-1c pathway and contributes to the pathogenesis of nonalcoholic steatohepatitis. Biochem Biophys Res Commun. 2018; 499(1):66-70. DOI: 10.1016/j.bbrc.2018.03.127. View