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Focus on long non-coding RNA MALAT1: Insights into acute and chronic lung diseases.

作者信息

Lai Xingning, Zhong Jie, Zhang Aihua, Zhang Boyi, Zhu Tao, Liao Ren

机构信息

Department of Anesthesiology, West China Hospital, Sichuan University, Chengdou, Sichuan, China.

Research Unit for Perioperative Stress Assessment and Clinical Decision, Chinese Academy of Medical Sciences (2018RU012), West China Hospital, Sichuan University, Chengdou, Sichuan, China.

出版信息

Front Genet. 2022 Sep 16;13:1003964. doi: 10.3389/fgene.2022.1003964. eCollection 2022.


DOI:10.3389/fgene.2022.1003964
PMID:36186445
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9523402/
Abstract

Acute lung injury (ALI) is a pulmonary illness with a high burden of morbidity and mortality around the world. Chronic lung diseases also represent life-threatening situations. Metastasis-associated lung adenocarcinoma transcript 1 (MALAT1) is a type of long non-coding RNA (lncRNA) and is highly abundant in lung tissues. MALAT1 can function as a competitive endogenous RNA (ceRNA) to impair the microRNA (miRNA) inhibition on targeted messenger RNAs (mRNAs). In this review, we summarized that MALAT1 mainly participates in pulmonary cell biology and lung inflammation. Therefore, MALAT1 can positively or negatively regulate ALI and chronic lung diseases (e.g., chronic obstructive pulmonary disease (COPD), bronchopulmonary dysplasia (BPD), pulmonary fibrosis, asthma, and pulmonary hypertension (PH)). Besides, we also found a MALAT1-miRNA-mRNA ceRNA regulatory network in acute and chronic lung diseases. Through this review, we hope to cast light on the regulatory mechanisms of MALAT1 in ALI and chronic lung disease and provide a promising approach for lung disease treatment.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5351/9523402/2021a8be6c5f/fgene-13-1003964-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5351/9523402/2021a8be6c5f/fgene-13-1003964-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5351/9523402/2021a8be6c5f/fgene-13-1003964-g001.jpg

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[1]
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引用本文的文献

[1]
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.

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[2]
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Int J Mol Sci. 2024-8-19

[3]
Long noncoding RNA MALAT1 in dermatologic disorders: a comprehensive review.

Biomark Med. 2024

[4]
Construction and Bioinformatics Analysis of ceRNA Regulatory Networks in Idiopathic Pulmonary Fibrosis.

Biochem Genet. 2024-6-13

[5]
Emerging role of long non-coding RNA MALAT1 related signaling pathways in the pathogenesis of lung disease.

Front Cell Dev Biol. 2023-5-11

[6]
Epigenetic regulation of pulmonary inflammation.

Semin Cell Dev Biol. 2024-2-15

[7]
Mechanisms Contributing to the Comorbidity of COPD and Lung Cancer.

Int J Mol Sci. 2023-2-2

[8]
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[9]
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本文引用的文献

[1]
AdMSC-derived exosomes alleviate acute lung injury via transferring mitochondrial component to improve homeostasis of alveolar macrophages.

Theranostics. 2022

[2]
Long non-coding RNA metastasis-related lung adenocarcinoma transcript 1 (MALAT1) forms a negative feedback loop with long non-coding RNA colorectal neoplasia differentially expressed (CRNDE) in sepsis to regulate lung cell apoptosis.

Bioengineered. 2022-4

[3]
March1-overexpressed dendritic cells downregulate Th1/Th2 ratio in asthma through promoting OX40L.

Int Immunopharmacol. 2022-2

[4]
Pulmonary Arterial Hypertension.

N Engl J Med. 2021-12-16

[5]
Downregulation of microRNA-512-3p enhances the viability and suppresses the apoptosis of vascular endothelial cells, alleviates autophagy and endoplasmic reticulum stress as well as represses atherosclerotic lesions in atherosclerosis by adjusting spliced/unspliced ratio of X-box binding protein 1 (XBP-1S/XBP-1U).

Bioengineered. 2021-12

[6]
Novel Insights Into Function as a MicroRNA Sponge in NSCLC.

Front Oncol. 2021-10-27

[7]
Effect of Methylation Status of lncRNA-MALAT1 and MicroRNA-146a on Pulmonary Function and Expression Level of COX2 in Patients With Chronic Obstructive Pulmonary Disease.

Front Cell Dev Biol. 2021-9-8

[8]
Minocycline attenuates oxidative and inflammatory injury in a intestinal perforation induced septic lung injury model via down-regulating lncRNA MALAT1 expression.

Int Immunopharmacol. 2021-11

[9]
Long non-coding RNA MALAT1 enhances the protective effect of dexmedetomidine on acute lung injury by sponging miR-135a-5p to downregulate the ratio of X-box binding proteins XBP-1S/XBP-1U.

Bioengineered. 2021-12

[10]
Pulmonary delivery of siRNA against acute lung injury/acute respiratory distress syndrome.

Acta Pharm Sin B. 2022-2

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