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Abstract
A sustained pro-oncogenic molecular signature was identified in severe COVID-19 patients' blood cells one year post-infection.
- Differential gene expression analysis showed significant changes in gene activity among severe COVID-19 patients compared to healthy controls and those with mild infections.
- Cancer-associated pathways related to cell death, viral-induced cancer, and gene regulatory processes were notably enriched in severe COVID-19 patients.
- The autophagy-related gene SQSTM1/P62 was identified as a key hub gene in severe COVID-19 patients, interacting with genes linked to inflammation and cancer progression.
- Higher expression of specific hub genes associated with COVID-19 was correlated with worse outcomes in various cancer types, including bladder and brain cancers.
- Severe COVID-19 infection may create a systemic environment that supports cancer development or recurrence, suggesting the need for ongoing cancer monitoring in affected individuals.
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