» Articles » PMID: 33533071

Long Non-coding RNAs: Promising New Targets in Pulmonary Fibrosis

Overview
Journal J Gene Med
Date 2021 Feb 3
PMID 33533071
Citations 17
Authors
Affiliations
Soon will be listed here.
Abstract

Pulmonary fibrosis is characterized by progressive and irreversible scarring in the lungs with poor prognosis and treatment. It is caused by various factors, including environmental and occupational exposures, and some rheumatic immune diseases. Even the rapid global spread of the COVID-19 pandemic can also cause pulmonary fibrosis with a high probability. Functions attributed to long non-coding RNAs (lncRNAs) make them highly attractive diagnostic and therapeutic targets in fibroproliferative diseases. Therefore, an understanding of the specific mechanisms by which lncRNAs regulate pulmonary fibrotic pathogenesis is urgently needed to identify new possibilities for therapy. In this review, we focus on the molecular mechanisms and implications of lncRNAs targeted protein-coding and non-coding genes during pulmonary fibrogenesis, and systematically analyze the communication of lncRNAs with various types of RNAs, including microRNA, circular RNA and mRNA. Finally, we propose the potential approach of lncRNA-based diagnosis and therapy for pulmonary fibrosis. We hope that understanding these interactions between protein-coding and non-coding genes will contribute to the development of lncRNA-based clinical applications for pulmonary fibrosis.

Citing Articles

Silicosis: from pathogenesis to therapeutics.

Yang B, Liu X, Peng C, Meng X, Jia Q Front Pharmacol. 2025; 16:1516200.

PMID: 39944632 PMC: 11813918. DOI: 10.3389/fphar.2025.1516200.


The Relationship Between Differential Expression of Non-coding RNAs (TP53TG1, LINC00342, MALAT1, DNM3OS, miR-126-3p, miR-200a-3p, miR-18a-5p) and Protein-Coding Genes (PTEN, FOXO3) and Risk of Idiopathic Pulmonary Fibrosis.

Korytina G, Markelov V, Gibadullin I, Zulkarneev S, Nasibullin T, Zulkarneev R Biochem Genet. 2025; .

PMID: 39881079 DOI: 10.1007/s10528-024-11012-z.


Biogenesis and Function of circRNAs in Pulmonary Fibrosis.

Zhang S, Hu W, Lv C, Song X Curr Gene Ther. 2024; 24(5):395-409.

PMID: 39005062 DOI: 10.2174/0115665232284076240207073542.


Construction and Bioinformatics Analysis of ceRNA Regulatory Networks in Idiopathic Pulmonary Fibrosis.

Zhang M, Wu X, Zhu H, Fu C, Yang W, Jing X Biochem Genet. 2024; .

PMID: 38871957 DOI: 10.1007/s10528-024-10853-y.


LINC01305 recruits basonuclin 1 to act on G-protein pathway suppressor 1 to promote esophageal squamous cell carcinoma.

Xiong L, Tan J, Zhang R, Long Q, Xiong R, Liu Y Cancer Sci. 2023; 114(11):4314-4328.

PMID: 37705202 PMC: 10637064. DOI: 10.1111/cas.15963.


References
1.
Lopez-Otin C, Blasco M, Partridge L, Serrano M, Kroemer G . The hallmarks of aging. Cell. 2013; 153(6):1194-217. PMC: 3836174. DOI: 10.1016/j.cell.2013.05.039. View

2.
Selman M, Pardo A . Revealing the pathogenic and aging-related mechanisms of the enigmatic idiopathic pulmonary fibrosis. an integral model. Am J Respir Crit Care Med. 2014; 189(10):1161-72. DOI: 10.1164/rccm.201312-2221PP. View

3.
Yan W, Wu Q, Yao W, Li Y, Liu Y, Yuan J . MiR-503 modulates epithelial-mesenchymal transition in silica-induced pulmonary fibrosis by targeting PI3K p85 and is sponged by lncRNA MALAT1. Sci Rep. 2017; 7(1):11313. PMC: 5596016. DOI: 10.1038/s41598-017-11904-8. View

4.
Sun H, Chen J, Qian W, Kang J, Wang J, Jiang L . Integrated long non-coding RNA analyses identify novel regulators of epithelial-mesenchymal transition in the mouse model of pulmonary fibrosis. J Cell Mol Med. 2016; 20(7):1234-46. PMC: 4929291. DOI: 10.1111/jcmm.12783. View

5.
Ozawa Y, Suda T, Naito T, Enomoto N, Hashimoto D, Fujisawa T . Cumulative incidence of and predictive factors for lung cancer in IPF. Respirology. 2009; 14(5):723-8. DOI: 10.1111/j.1440-1843.2009.01547.x. View