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pmid:35497924

m6A RNA Methylation Regulators Contribute to Predict and as a Therapy Target of Pulmonary Fibrosis.

Meng-Sheng Deng · Kui-Jun Chen · Dong-Dong Zhang · Guan-Hua Li · Chang-Mei Weng · Jian-Min Wang

Evidence-based complementary and alternative medicine : eCAM · 2022 doi:10.1155/2022/2425065

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complete

Experiment

complete

Data

partial

Analysis

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Execution

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title
m6A RNA Methylation Regulators Contribute to Predict and as a Therapy Target of Pulmonary Fibrosis.
doi
10.1155/2022/2425065
pmid
35497924
authors array · 6 items
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Meng-Sheng Deng
[1]
Kui-Jun Chen
[2]
Dong-Dong Zhang
[3]
Guan-Hua Li
[4]
Chang-Mei Weng
[5]
Jian-Min Wang
journal
Evidence-based complementary and alternative medicine : eCAM
year
2022
abstract
Background: Pulmonary fibrosis is difficult to treat. Early diagnosis and finding potential drug therapy targets of pulmonary fibrosis are particularly important. There were still various problems with existing pulmonary fibrosis markers, so it is particularly important to find new biomarkers and drug treatment targets. m6A (N6,2'-O-dimethyladenosine) RNA methylation was the cause of many diseases, and it is regulated by m6A methylation regulators. So, whether RNA methylation regulators can be a diagnostic marker and potential drug therapy target of early pulmonary fibrosis needs to be explored. Materials and Methods: Using GSE110147 and GSE33566 in the GEO database to predict the m6A methylation regulators that may be related to the development of pulmonary fibrosis, we used 10 mg/ml bleomycin to induce mouse pulmonary fibrosis models and human pulmonary fibrosis samples, to confirm whether this indicator can be an early diagnostic marker of pulmonary fibrosis. Results: According to the database prediction results, METTL3 can predict the occurrence and development of pulmonary fibrosis, and the results of MASSON and HE staining show that the fibrosis model of mice is successful, and the fibrosis of human samples is obvious. The results of immunohistochemistry showed that the expression of METTL3 was significantly reduced in pulmonary fibrosis. Conclusions: The m6A methylation regulator METTL3 can be considered as an important biomarker for diagnosing pulmonary fibrosis occurrence, furthermore it could be considered as a drug target because of its low expression in pulmonary fibrosis.
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brosis, we used 10 mg/ml bleomycin to induce mouse pulmonary fibrosis models and human pulmonar
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amount of normal saline. After 28 days, the mice were sacrificed, and their lung tissues were collected. All
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:35497924", "kind": "science-record", "revision": 3, "content_hash": "sha256:5e853bc4537275677da4d6bf5fe87ff34917d8e099c92a35b1518714d0f7e066", "created_at": "2026-11-01T18:14:22Z", "updated_at": "2026-11-01T21:27:45Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "m6A RNA Methylation Regulators Contribute to Predict and as a Therapy Target of Pulmonary Fibrosis.", "doi": "10.1155/2022/2425065", "pmid": "35497924", "authors": ["Meng-Sheng Deng", "Kui-Jun Chen", "Dong-Dong Zhang", "Guan-Hua Li", "Chang-Mei Weng", "Jian-Min Wang"], "journal": "Evidence-based complementary and alternative medicine : eCAM", "year": 2022, "abstract": "Background: Pulmonary fibrosis is difficult to treat. Early diagnosis and finding potential drug therapy targets of pulmonary fibrosis are particularly important. There were still various problems with existing pulmonary fibrosis markers, so it is particularly important to find new biomarkers and drug treatment targets. m6A (N6,2'-O-dimethyladenosine) RNA methylation was the cause of many diseases, and it is regulated by m6A methylation regulators. So, whether RNA methylation regulators can be a diagnostic marker and potential drug therapy target of early pulmonary fibrosis needs to be explored.\nMaterials and Methods: Using GSE110147 and GSE33566 in the GEO database to predict the m6A methylation regulators that may be related to the development of pulmonary fibrosis, we used 10 mg/ml bleomycin to induce mouse pulmonary fibrosis models and human pulmonary fibrosis samples, to confirm whether this indicator can be an early diagnostic marker of pulmonary fibrosis.\nResults: According to the database prediction results, METTL3 can predict the occurrence and development of pulmonary fibrosis, and the results of MASSON and HE staining show that the fibrosis model of mice is successful, and the fibrosis of human samples is obvious. The results of immunohistochemistry showed that the expression of METTL3 was significantly reduced in pulmonary fibrosis.\nConclusions: The m6A methylation regulator METTL3 can be considered as an important biomarker for diagnosing pulmonary fibrosis occurrence, furthermore it could be considered as a drug target because of its low expression in pulmonary fibrosis.", "claims": [{"id": "claim-method", "statement": "Logistic regression demonstrated strong correlations with m6A methylation regulators in pulmonary fibrosis (Table 1).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:35497924", "locator": "sections[11] \"3.2. 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