Immune Infiltration and N(6)-Methyladenosine ncRNA Isoform Detection in Acute Lung Injury

Author:

Gu Chenzheng1ORCID,Li Caiyun2ORCID,Wang Weiwei3ORCID,Yan Wenhui4ORCID,Yao Yiwen5ORCID,Shi Meng6ORCID,Han Fei7ORCID,Shang Anquan1ORCID

Affiliation:

1. Department of Laboratory Medicine, Shanghai Tongji Hospital, School of Medicine, Tongji University, Shanghai 200065, China

2. Department of Laboratory Medicine, Pukou Branch of Jiangsu People’s Hospital & Nanjing Pukou Dictrict Central Hospital, Nanjing 211800, Jiangsu, China

3. Department of Pathology, Tinghu People’s Hospital of Yancheng City, Yancheng 224005, Jiangsu, China

4. Department of Laboratory Medicine, Yangzhi Rehabilitation Hospital (Shanghai Sunshine Rehabilitation Center), Tongji Univeirsity School of Medicine, Shanghai 201619, China

5. Department of Internal Medicine V-Pulmonology, Allergology, Respiratory Intensive Care Medicine, Saarland University Hospital, Homburg 66424, Germany

6. Department of Cardiothoracic Surgery, Huashan Hospital, Fudan University, Shanghai 200040, China

7. Department of Laboratory Medicine, The Fourth Affiliated Hospital of Nanjing Medical University, Nanjing 210031, Jiangsu, China

Abstract

Acute lung injury (ALI) is a severe form of sepsis that is associated with a high rate of morbidity and death in critically ill individuals. The emergence of ALI is the result of several factors at work. Case mortality rates might range from 40% to 70%. Researchers have discovered that epigenetic alterations are important in the pathophysiology of ALI and that using epigenetic inhibitors may help reduce symptoms. In embryonic development, circadian rhythm, the cell cycle, and cancer, methylation of m6A seems to be relevant all along the way. According to recent research, posttranscriptional methylation is a key player in the development of alveolar lymphoma. In this study, we clustered ALI based on m6A-related factors, analyzed different classes of immune cell enrichment and inflammatory cytokine expression, screened clustered differential genes for ALI to construct coexpression networks, screened key ALI genes potentially regulated by m6A modifications, and then typed the disease based on key genes to compare the consistency of different clustering results. Our findings have revealed a hitherto undiscovered prognostic sign and a therapeutic target for ALI therapy in m6A and immune invading cells, respectively.

Funder

China Postdoctoral Science Foundation

Publisher

Hindawi Limited

Subject

Oncology

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