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北京京煤集团总医院 第十届·2022 学术年会论文集
daunorubicin is a potential therapeutic drug against SARS-CoV-2 [46]. In this study, candidate drugs
that interacted with overlapped DEGs were identified, and the top 10 drugs with the most significant
potential were lanatoside C, digoxin, GW-8510, doxorubicin, daunorubicin, proscillaridin,
anisomycin, helveticoside, ouabain, and bisacodyl. Thus, these drugs may offer novel options for
improving COVID-19 and asthma treatment.
However, this study has some limitations. First, the data used in this study were downloaded
from a public database, and more relevant experiments should be conducted to validate the identified
hub genes and drugs. Second, further studies should be conducted to analyze the detailed
mechanisms of FOXC1, GATA2, hsa-miR-93-5p, and hsa-miR-17-5p in the progression of COVID-
19/asthma. Third, clinical evidence is required to support the targets and drugs identified in this
study.
5. Conclusions
This study identified potential biomarkers for COVID-19 and asthma and predicted druggable
targets against COVID-19/asthma comorbidity. Thus, this study provides a novel clarification of
COVID-19/asthma comorbidity treatment.
6. Statements & Declarations
Acknowledgments We acknowledge the GEO database for providing its platform and the
contributors for uploading their valuable datasets.
Funding The authors declare that no funds, grants, or other supports have been received during the
preparation of this manuscript.
Conflict of Interest The authors have no relevant financial or non-financial interests to disclose.
Author Contributions All authors contributed to the study conception and design. All authors read
and approved the final version of the manuscript.
Data availability The datasets generated and/or analyzed in the current study are available in the
GEO (https://www.ncbi.nlm.nih.gov/geo/) database.
Ethics Approval Ethics approval was waived for this study because all the analyses performed in
this study were based on open-source data from public databases.
Consent to Participate Not applicable.
Consent to Publish Not applicable.
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