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The miR-15b-Smurf2-HSP27 axis promotes pulmonary fibrosis

Authors
 Seulgi Jeon  ;  Hee Jin  ;  Jin-Mo Kim  ;  Youmin Hur  ;  Eun Joo Song  ;  Yoon-Jin Lee  ;  Younghwa Na  ;  Jaeho Cho  ;  Yun-Sil Lee 
Citation
 JOURNAL OF BIOMEDICAL SCIENCE, Vol.30(1) : 2, 2023-01 
Journal Title
JOURNAL OF BIOMEDICAL SCIENCE
ISSN
 1021-7770 
Issue Date
2023-01
MeSH
Animals ; Epithelial-Mesenchymal Transition ; HSP27 Heat-Shock Proteins / genetics ; HSP27 Heat-Shock Proteins / metabolism ; HSP27 Heat-Shock Proteins / pharmacology ; Mice ; MicroRNAs* / metabolism ; Pulmonary Fibrosis* / genetics ; RNA, Messenger ; Ubiquitin-Protein Ligases / genetics
Keywords
HSP27 ; Phosphorylation ; Protein degradation ; Pulmonary fibrosis ; Smurf2 ; miRNA
Abstract
Background: Heat shock protein 27 (HSP27) is overexpressed during pulmonary fibrosis (PF) and exacerbates PF; however, the upregulation of HSP27 during PF and the therapeutic strategy of HSP27 inhibition is not well elucidated.

Methods: We have developed a mouse model simulating clinical stereotactic body radiotherapy (SBRT) with focal irradiation and validated the induction of RIPF. HSP25 (murine form of HSP27) transgenic (TG) and LLC1-derived orthotropic lung tumor models were also used. Lung tissues of patients with RIPF and idiopathic pulmonary fibrosis, and lung tissues from various fibrotic mouse models, as well as appropriated cell line systems were used. Public available gene expression datasets were used for therapeutic response rate analysis. A synthetic small molecule HSP27 inhibitor, J2 was also used.

Results: HSP27 expression with its phosphorylated form (pHSP27) increased during PF. Decreased mRNA expression of SMAD-specific E3 ubiquitin-protein ligase 2 (Smurf2), which is involved in ubiquitin degradation of HSP27, was responsible for the increased expression of pHSP27. In addition, increased expression of miRNA15b was identified with decreased expression of Smurf2 mRNA in PF models. Inverse correlation between pHSP27 and Smurf2 was observed in the lung tissues of PF animals, an irradiated orthotropic lung cancer models, and PF tissues from patients. Moreover, a HSP27 inhibitor cross-linked with HSP27 protein to ameliorate PF, which was more effective when targeting the epithelial to mesenchymal transition (EMT) stage of PF.

Conclusions: Our findings identify upregulation mechanisms of HSP27 during PF and provide a therapeutic strategy for HSP27 inhibition for overcoming PF.
Files in This Item:
T202300950.pdf Download
DOI
10.1186/s12929-023-00896-5
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Radiation Oncology (방사선종양학교실) > 1. Journal Papers
Yonsei Authors
Cho, Jae Ho(조재호) ORCID logo https://orcid.org/0000-0001-9966-5157
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/193585
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