# Tetrandrine-driven autophagy suppresses SARS-CoV-2 replication by modulating cholesterol and IGF signaling pathways

**Authors:** Lais de O. Marchioro, Sofia De Stefanis, Beatriz G. Araújo, Davide Mariotti, Ingrid K. M. Watanabe, Michael Stumpe, Giulia Matusali, Fabrizio Maggi, Soraya S. Smaili, Jörn Dengjel, Gustavo J. S. Pereira, Manuela Antonioli

PMC · DOI: 10.1038/s41420-025-02926-7 · Cell Death Discovery · 2026-01-06

## TL;DR

Tetrandrine, a natural compound, suppresses SARS-CoV-2 replication in lung cells by modulating autophagy and other host pathways.

## Contribution

The study reveals Tetrandrine's antiviral effects against SARS-CoV-2 via both autophagy-dependent and -independent mechanisms.

## Key findings

- Tetrandrine reduces SARS-CoV-2 replication in Calu-3 cells, especially when administered before infection.
- Proteomic analysis shows Tetrandrine affects autophagy, cholesterol metabolism, and IGF signaling pathways.
- Antiviral effects persist in autophagy-deficient cells, suggesting additional mechanisms are involved.

## Abstract

SARS-CoV-2 exploits multiple host cellular processes, including autophagy, a critical intracellular degradation pathway, to facilitate viral replication and evade immune detection. Tetrandrine, a natural bis-benzylisoquinoline alkaloid derived from Stephania tetrandra, has been reported to modulate autophagy and exhibits potential antiviral properties. In this study, we investigated the effects of Tetrandrine on SARS-CoV-2 infection in human lung epithelial cells (Calu-3), with a particular focus on autophagy-related mechanisms. Our results demonstrate that Tetrandrine modulates autophagic activity in a dose-dependent manner and significantly reduces SARS-CoV-2 replication, particularly when administered prior to infection. Notably, its antiviral effect is retained in autophagy-deficient cells, indicating the involvement of autophagy-independent mechanisms. Proteomic analysis of Calu-3 cells infected with the Omicron BA.5 variant revealed that Tetrandrine regulates several host pathways implicated in viral replication, including autophagy, cholesterol metabolism, and insulin-like growth factor signaling. These findings suggest that Tetrandrine exerts multifaceted antiviral effects by targeting both autophagy-dependent and -independent cellular pathways. Collectively, our data supports the potential of Tetrandrine as a therapeutic candidate against COVID-19 and warns further evaluation in preclinical and clinical models. Data are available via ProteomeXchange with identifier PXD064448.

## Linked entities

- **Chemicals:** Tetrandrine (PubChem CID 73078)
- **Diseases:** SARS-CoV-2 (MONDO:0100096), COVID-19 (MONDO:0100096)

## Full-text entities

- **Diseases:** infection (MESH:D007239), COVID-19 (MESH:D000086382)
- **Chemicals:** Tetrandrine (MESH:C009438), cholesterol (MESH:D002784), bis-benzylisoquinoline alkaloid (-)
- **Species:** Botryodiscia tetrandra (species) [taxon 425106], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12877079/full.md

## References

18 references — full list in the complete paper: https://tomesphere.com/paper/PMC12877079/full.md

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Source: https://tomesphere.com/paper/PMC12877079