Upregulation of receptor tyrosine kinase-like orphan receptor 2 in idiopathic pulmonary fibrosis
Background/Aims Receptor tyrosine kinase-like orphan receptor 2 (ROR2) is a major regulator of Wnt signaling, which is involved in fibroblast dysfunction. Because its role has not been evaluated in idiopathic pulmonary fibrosis (IPF), we examined the clinical implications of ROR2 expression. Methods...
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doaj-8650283cca794a47a23f688cea7f2ab02021-08-10T05:57:57ZengThe Korean Association of Internal MedicineThe Korean Journal of Internal Medicine1226-33032005-66482021-07-0136491492310.3904/kjim.2019.270170480Upregulation of receptor tyrosine kinase-like orphan receptor 2 in idiopathic pulmonary fibrosisJi-Hye Son0Jong-Uk Lee1Susie Chin2Eun-Suk Go3Jai-Seong Park4Hwa-Kyun Shin5Hun Soo Chang6Jong-Sook Park7Choon-Sik Park8 Department of Interdisciplinary Program in Biomedical Science Major, Graduate School, Soonchunhyang University, Asan, Korea Genome Research Center and Division of Allergy and Respiratory Medicine, Department of Internal Medicine, Soonchunhyang University Bucheon Hospital, Bucheon, Korea Department of Pathology, Soonchunhyang University Bucheon Hospital, Bucheon, Korea Department of Pathology, Soonchunhyang University College of Medicine, Asan, Korea Department of Radiology, Soonchunhyang University College of Medicine, Asan, Korea Department of Thoracic Surgery, Soonchunhyang University College of Medicine, Asan, Korea Department of Interdisciplinary Program in Biomedical Science Major, Graduate School, Soonchunhyang University, Asan, Korea Genome Research Center and Division of Allergy and Respiratory Medicine, Department of Internal Medicine, Soonchunhyang University Bucheon Hospital, Bucheon, Korea Genome Research Center and Division of Allergy and Respiratory Medicine, Department of Internal Medicine, Soonchunhyang University Bucheon Hospital, Bucheon, KoreaBackground/Aims Receptor tyrosine kinase-like orphan receptor 2 (ROR2) is a major regulator of Wnt signaling, which is involved in fibroblast dysfunction. Because its role has not been evaluated in idiopathic pulmonary fibrosis (IPF), we examined the clinical implications of ROR2 expression. Methods ROR2 mRNA expression was measured using reverse transcription polymerase chain reaction in lung tissue-derived fibroblasts from IPF patients (n = 14) and from controls (n = 10). ROR2 protein was measured using enzyme-linked immunosorbent assay in primary fibroblasts from IPF patients (n = 14) and controls (n = 10), and in bronchoalveolar lavage (BAL) fluids obtained from normal controls (NC; n = 30). IPF patients (n = 84), and other patients with interstitial lung diseases, including nonspecific interstitial pneumonia (NSIP; n = 10), hypersensitivity pneumonitis (HP; n = 10), and sarcoidosis (n = 10). Results ROR2 mRNA and protein levels were significantly higher in IPF fibroblasts than in controls (p = 0.003, p = 0.0017, respectively). ROR2 protein levels in BAL fluids from patients with IPF were significantly higher than in those from NC (p < 0.001), and from patients with NSIP (p = 0.006), HP (p = 0.004), or sarcoidosis (p = 0.004). Receiver operating characteristic curves showed a clear difference between IPF and NC in ROR2 protein level (area under the curve, 0.890; confidence interval, 0.829 to 0.950; p < 0.001). ROR2 protein levels were significantly higher in GAP stage III than in GAP stages I and II (p = 0.016). Conclusions ROR2 may be related to the development of IPF, and its protein level may be a useful and severity-dependent candidate marker for IPF.http://www.kjim.org/upload/pdf/kjim-2019-270.pdfidiopathic pulmonary fibrosisreceptor tyrosine kinase-like orphan receptorsbronchoalveolar lavage fluiddifferential diagnosis |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Ji-Hye Son Jong-Uk Lee Susie Chin Eun-Suk Go Jai-Seong Park Hwa-Kyun Shin Hun Soo Chang Jong-Sook Park Choon-Sik Park |
spellingShingle |
Ji-Hye Son Jong-Uk Lee Susie Chin Eun-Suk Go Jai-Seong Park Hwa-Kyun Shin Hun Soo Chang Jong-Sook Park Choon-Sik Park Upregulation of receptor tyrosine kinase-like orphan receptor 2 in idiopathic pulmonary fibrosis The Korean Journal of Internal Medicine idiopathic pulmonary fibrosis receptor tyrosine kinase-like orphan receptors bronchoalveolar lavage fluid differential diagnosis |
author_facet |
Ji-Hye Son Jong-Uk Lee Susie Chin Eun-Suk Go Jai-Seong Park Hwa-Kyun Shin Hun Soo Chang Jong-Sook Park Choon-Sik Park |
author_sort |
Ji-Hye Son |
title |
Upregulation of receptor tyrosine kinase-like orphan receptor 2 in idiopathic pulmonary fibrosis |
title_short |
Upregulation of receptor tyrosine kinase-like orphan receptor 2 in idiopathic pulmonary fibrosis |
title_full |
Upregulation of receptor tyrosine kinase-like orphan receptor 2 in idiopathic pulmonary fibrosis |
title_fullStr |
Upregulation of receptor tyrosine kinase-like orphan receptor 2 in idiopathic pulmonary fibrosis |
title_full_unstemmed |
Upregulation of receptor tyrosine kinase-like orphan receptor 2 in idiopathic pulmonary fibrosis |
title_sort |
upregulation of receptor tyrosine kinase-like orphan receptor 2 in idiopathic pulmonary fibrosis |
publisher |
The Korean Association of Internal Medicine |
series |
The Korean Journal of Internal Medicine |
issn |
1226-3303 2005-6648 |
publishDate |
2021-07-01 |
description |
Background/Aims Receptor tyrosine kinase-like orphan receptor 2 (ROR2) is a major regulator of Wnt signaling, which is involved in fibroblast dysfunction. Because its role has not been evaluated in idiopathic pulmonary fibrosis (IPF), we examined the clinical implications of ROR2 expression. Methods ROR2 mRNA expression was measured using reverse transcription polymerase chain reaction in lung tissue-derived fibroblasts from IPF patients (n = 14) and from controls (n = 10). ROR2 protein was measured using enzyme-linked immunosorbent assay in primary fibroblasts from IPF patients (n = 14) and controls (n = 10), and in bronchoalveolar lavage (BAL) fluids obtained from normal controls (NC; n = 30). IPF patients (n = 84), and other patients with interstitial lung diseases, including nonspecific interstitial pneumonia (NSIP; n = 10), hypersensitivity pneumonitis (HP; n = 10), and sarcoidosis (n = 10). Results ROR2 mRNA and protein levels were significantly higher in IPF fibroblasts than in controls (p = 0.003, p = 0.0017, respectively). ROR2 protein levels in BAL fluids from patients with IPF were significantly higher than in those from NC (p < 0.001), and from patients with NSIP (p = 0.006), HP (p = 0.004), or sarcoidosis (p = 0.004). Receiver operating characteristic curves showed a clear difference between IPF and NC in ROR2 protein level (area under the curve, 0.890; confidence interval, 0.829 to 0.950; p < 0.001). ROR2 protein levels were significantly higher in GAP stage III than in GAP stages I and II (p = 0.016). Conclusions ROR2 may be related to the development of IPF, and its protein level may be a useful and severity-dependent candidate marker for IPF. |
topic |
idiopathic pulmonary fibrosis receptor tyrosine kinase-like orphan receptors bronchoalveolar lavage fluid differential diagnosis |
url |
http://www.kjim.org/upload/pdf/kjim-2019-270.pdf |
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