COVID-19 Research Paper Volume 13, Issue 2 pp 1620—1632
Lung adenocarcinoma patients have higher risk of SARS-CoV-2 infection
- 1 Bioengineering Institute of Chongqing University, Chongqing, China
- 2 Three Gorges Central Hospital, Wanzhou, Chongqing, China
- 3 Chongqing Mix Biotechnology Co., Ltb, Chongqing, China
Received: June 11, 2020 Accepted: July 30, 2020 Published: January 10, 2021https://doi.org/10.18632/aging.202375
How to Cite
Copyright: © 2021 Chen et al. This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Both lung adenocarcinoma and coronavirus disease 2019 would cause pulmonary inflammation. Angiotensin-converting enzyme 2, the functional receptor of SARS-CoV-2, also plays a key role in lung adenocarcinoma. To study the risk of SARS-CoV-2 infection in lung adenocarcinoma patients, mRNA and microRNA profiles were obtained from The Cancer Genome Atlas and Gene Expression Omnibus followed by bioinformatics analysis. A network which regards angiotensin-converting enzyme 2 as the center was structured. In addition, via immunological analysis to explore the essential mechanism of SARS-CoV-2 susceptibility in lung adenocarcinoma. Compared with normal tissue, angiotensin-converting enzyme 2 was increased in lung adenocarcinoma patients. Furthermore, a total of 7 correlated differently expressed mRNAs (ACE2, CXCL9, MMP12, IL6, AZU1, FCN3, HYAL1 and IRAK3) and 5 correlated differently expressed microRNAs (miR-125b-5p, miR-9-5p, miR-130b-5p, miR-381-3p and miR-421) were screened. Interestingly, the most frequent toll-like receptor signaling pathway was enriched by mRNA (interlukin 6) and miRNA (miR-125b-5p) sets simultaneously. In conclusion, it was assumed that miR-125b-5p-ACE2-IL6 axis could alter the risk of SARS-CoV-2 infection in lung adenocarcinoma patients.
COVID-19: coronavirus pneumonia-19; ACE2: angiotensin-converting enzyme 2; Ang II: angiotensin II; Ang 1-7: angiotensin 1-7; RAS: renin-angiotensin system; LUAD: lung adenocarcinoma; NSCLC: non-small cell lung cancer; KEGG: Kyoto Encyclopaedia of Genes and Genomes; SEM: standard error of the mean; MasR: Mas receptor; DECG: differentially expressed correlative gene; DECM: differentially expressed correlative miRNA; RAS: renin-angiotensin system; GM-CSF: granulocyte-macrophage colony-stimulating factors.