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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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