Long non-coding RNAs: Promising new targets in pulmonary fibrosis

被引:22
|
作者
Zhang, Songzi [1 ,2 ]
Chen, Hongbin [1 ]
Yue, Dayong [1 ]
Blackwell, Timothy S. [3 ]
Lv, Changjun [1 ,2 ]
Song, Xiaodong [1 ,2 ]
机构
[1] Binzhou Med Univ, Sch Pharmaceut Sci, Dept Cellular & Genet Med, Yantai, Peoples R China
[2] Binzhou Med Univ, Affiliated Hosp, Dept Resp Med, Binzhou, Peoples R China
[3] Vanderbilt Univ, Med Ctr, Nashville, TN USA
来源
JOURNAL OF GENE MEDICINE | 2021年 / 23卷 / 03期
基金
中国国家自然科学基金;
关键词
circular RNA; COVID-19; lncRNA; microRNA; pulmonary fibrosis; EPITHELIAL-MESENCHYMAL TRANSITION; LNCRNA; EXPRESSION; GENE; CANCER; TRANSCRIPTION; INHIBITION; ACTIVATION; MECHANISMS; DIAGNOSIS;
D O I
10.1002/jgm.3318
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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.
引用
收藏
页数:13
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