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Updated: Oct 9, 2025

Author Spotlight: Understanding Cytokine-Induced Cell Death in Intestinal Epithelial Cells Using Human Organoids
Published on: August 2, 2024
Coronavirus Infection-Associated Cell Death Signaling and Potential Therapeutic Targets
Rittibet Yapasert1, Patompong Khaw-On2, Ratana Banjerdpongchai1
1Department of Biochemistry, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.
Abstract:
COVID-19 is the name of the disease caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection that occurred in 2019. The virus-host-specific interactions, molecular targets on host cell deaths, and the involved signaling are crucial issues, which become potential targets for treatment. Spike protein, angiotensin-converting enzyme 2 (ACE2), cathepsin L-cysteine peptidase, transmembrane protease serine 2 (TMPRSS2), nonstructural protein 1 (Nsp1), open reading frame 7a (ORF7a), viral main protease (3C-like protease (3CLpro) or Mpro), RNA dependent RNA polymerase (RdRp) (Nsp12), non-structural protein 13 (Nsp13) helicase, and papain-like proteinase (PLpro) are molecules associated with SARS-CoV infection and propagation. SARS-CoV-2 can induce host cell death via five kinds of regulated cell death, i.e., apoptosis, necroptosis, pyroptosis, autophagy, and PANoptosis. The mechanisms of these cell deaths are well established and can be disrupted by synthetic small molecules or natural products. There are a variety of compounds proven to play roles in the cell death inhibition, such as pan-caspase inhibitor (z-VAD-fmk) for apoptosis, necrostatin-1 for necroptosis, MCC950, a potent and specific inhibitor of the NLRP3 inflammasome in pyroptosis, and chloroquine/hydroxychloroquine, which can mitigate the corresponding cell death pathways. However, NF-κB signaling is another critical anti-apoptotic or survival route mediated by SARS-CoV-2. Such signaling promotes viral survival, proliferation, and inflammation by inducing the expression of apoptosis inhibitors such as Bcl-2 and XIAP, as well as cytokines, e.g., TNF. As a result, tiny natural compounds functioning as proteasome inhibitors such as celastrol and curcumin can be used to modify NF-κB signaling, providing a responsible method for treating SARS-CoV-2-infected patients. The natural constituents that aid in inhibiting viral infection, progression, and amplification of coronaviruses are also emphasized, which are in the groups of alkaloids, flavonoids, terpenoids, diarylheptanoids, and anthraquinones. Natural constituents derived from medicinal herbs have anti-inflammatory and antiviral properties, as well as inhibitory effects, on the viral life cycle, including viral entry, replication, assembly, and release of COVID-19 virions. The phytochemicals contain a high potential for COVID-19 treatment. As a result, SARS-CoV-2-infected cell death processes and signaling might be of high efficacy for therapeutic targeting effects and yielding encouraging outcomes.
Insights
This study explores how SARS-CoV-2 causes cell death and how natural compounds can target these processes. Targeting virus-host interactions and cell death pathways offers promising therapeutic strategies for COVID-19 treatment.
Area of Science:
- Virology and Molecular Biology
- Immunology and Inflammation
- Pharmacology and Drug Discovery
Background:
- Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection leads to COVID-19, involving complex virus-host interactions.
- Understanding molecular targets and signaling pathways, including regulated cell death (apoptosis, necroptosis, pyroptosis, autophagy, PANoptosis), is crucial for developing treatments.
- The NF-κB signaling pathway plays a key role in viral survival, proliferation, and inflammation, presenting another therapeutic target.
Purpose of the Study:
- To investigate the molecular mechanisms of SARS-CoV-2-induced host cell death.
- To identify potential therapeutic targets within virus-host interactions and cell death signaling pathways.
- To explore the potential of natural compounds in modulating these pathways for COVID-19 treatment.
Main Methods:
- Review of literature on SARS-CoV-2 molecular targets and host cell death mechanisms.
- Analysis of signaling pathways, including NF-κB, involved in viral propagation and host response.
- Identification of natural compounds and their mechanisms of action against viral infection and cell death.
Main Results:
- SARS-CoV-2 utilizes specific viral molecules (e.g., Spike protein, ACE2, TMPRSS2, Mpro, RdRp) for entry and replication.
- The virus induces various forms of regulated cell death, which can be modulated by small molecules and natural products.
- Natural compounds like celastrol and curcumin can inhibit NF-κB signaling, while others like alkaloids and flavonoids exhibit antiviral properties.
Conclusions:
- Targeting SARS-CoV-2-induced cell death processes and signaling pathways offers high therapeutic potential.
- Natural constituents from medicinal herbs demonstrate significant anti-inflammatory and antiviral properties against coronaviruses.
- Phytochemicals represent a promising avenue for developing effective COVID-19 treatments by inhibiting viral life cycle and host responses.
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