# In Vitro Investigation of Statin Effects on Genes Associated with Severe COVID-19 in Cancerous and Non-Cancerous Cells

**Authors:** Adriana Kapustová, Patrik Macášek, Bibiána Baďurová, Jana Melegová, Silvie Rimpelová, Jan Kubovčiak, Jana Šáchová, Miluše Hradilová, Michal Kolář, Libor Vítek, Tomáš Ruml, Helena Gbelcová

PMC · DOI: 10.3390/biomedicines13071714 · 2025-07-14

## TL;DR

This study explores how statins affect genes linked to severe COVID-19 in cancerous and non-cancerous cells.

## Contribution

The study reveals that statins influence genes related to immune response, potentially affecting the progression of severe COVID-19.

## Key findings

- Statin use did not alter the expression of APOE and ACE2 genes linked to severe COVID-19.
- Some statins changed the expression of genes encoding interaction partners of APOE and ACE2.
- Statin treatment affected genes related to IL-6, IL-8, and NF-kB, which may influence viral persistence.

## Abstract

Background: The progressive course of coronavirus disease 2019 (COVID-19) is more frequently observed in individuals with obesity, diabetes, pulmonary and cardiovascular disease, or arterial hypertension. Many patients with these conditions are prescribed statins to treat hypercholesterolaemia. However, statins exhibit additional pleiotropic effects. The present study aims to investigate the effects of all eight currently existing statins on the expression of genes whose products have been reported to be directly associated with complicated COVID-19 disease. Methods: We extended the interpretation of the whole-genome DNA microarray analyses of pancreatic cancer cells MiaPaCa-2 and whole-transcriptome analyses of adipose tissue-derived mesenchymal stem cells AD-MSC that we had performed in the past. From the number of genes with altered expression induced by statins, we focused on those reported to be involved in a complicated course of COVID-19, including APOE and ACE2, genes encoding proteins involved in innate antiviral immunity and respiratory failure genes. Results: Although we did not observe statin-induced changes in the expression of APOE, ACE2 and any of the six genes clustered in the locus associated with respiratory failure in patients with COVID-19, some statins induced changes in the expression of genes encoding their interaction partners. Among genes associated with the immune system, all statins, which are effective in vitro affected the expression of genes encoding IL-6 and IL-8 and interaction partners of NF-kB, which may influence the duration of viral persistence. Conclusions: Statins act on multiple pathways simultaneously, some of which support COVID-19 development, while others suppress it.

## Linked entities

- **Genes:** APOE (apolipoprotein E) [NCBI Gene 348], ACE2 (angiotensin converting enzyme 2) [NCBI Gene 59272], IL6 (interleukin 6) [NCBI Gene 3569], CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576], NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790]
- **Diseases:** coronavirus disease 2019 (MONDO:0100096), obesity (MONDO:0011122), diabetes (MONDO:0005015), pulmonary disease (MONDO:0005275), cardiovascular disease (MONDO:0004995), pancreatic cancer (MONDO:0005192)

## Full-text entities

- **Genes:** APOE (apolipoprotein E) [NCBI Gene 348] {aka AD2, APO-E, ApoE4, LDLCQ5, LPG}, ACE2 (angiotensin converting enzyme 2) [NCBI Gene 59272] {aka ACEH}, CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}
- **Diseases:** diabetes (MESH:D003920), obesity (MESH:D009765), COVID-19 (MESH:D000086382), pulmonary and cardiovascular disease (MESH:D002318), arterial hypertension (MESH:D000081029), pancreatic cancer (MESH:D010190), respiratory failure (MESH:D012131), AD (MESH:D000544)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** MiaPaCa-2 — Homo sapiens (Human), Pancreatic undifferentiated carcinoma, Cancer cell line (CVCL_0428)

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12292488/full.md

---
Source: https://tomesphere.com/paper/PMC12292488