Letter to the editor

Triterpenoid saponins and ferroptosis: A membrane centered perspective

Tae Kyung Hyun1[*]

1Department of Industrial Plant Science and Technology, College of Agriculture, Life and Environment Sciences, Chungbuk National University, Cheongju 28644, Republic of Korea

EXCLI J 2026;25:Doc822

 



Ferroptosis is an iron-dependent form of regulated cell death driven by phospholipid peroxidation and membrane damage (Yang and Gao, 2026[9]). Unlike apoptosis and necrosis, ferroptosis is triggered by impaired detoxification of lipid hydroperoxides following disruption of glutathione peroxidase 4 (GPX4), resulting in uncontrolled membrane lipid oxidation (Li et al., 2020[4]). Recent studies indicate that ferroptotic susceptibility is strongly influenced by phospholipid composition, iron dependent redox activity, and membrane vulnerability to lipid peroxidation (Cui and Ye, 2026[1]; Yang and Gao, 2026[9]). Importantly, many ferroptosis associated pathways converge on membrane lipid peroxidation, suggesting that membrane organization may regulate ferroptotic sensitivity. In this context, membrane active natural compounds may represent previously underrecognized modulators of ferroptotic vulnerability.

Triterpenoid saponins are a structurally diverse class of amphiphilic plant metabolites composed of hydrophobic triterpene backbones linked to hydrophilic sugar moieties. Owing to their intrinsic affinity for biological membranes, these compounds can alter membrane organization, lipid dynamics, and membrane-associated redox processes (Zhong et al., 2025[10]). Accordingly, triterpenoid saponins have attracted attention for their broad pharmacological activities, including anticancer, immunomodulatory, and anti-inflammatory effects (Ouyang et al., 2025[6]). However, the mechanisms underlying their effects on regulated cell death pathways remain incompletely understood.

A major unresolved issue is that many cellular responses associated with triterpenoid saponin-induced cytotoxicity overlap with generalized oxidative injury, making it difficult to distinguish ferroptotic signaling from secondary oxidative damage (Podolak et al., 2023[7]). Nevertheless, several triterpenoid saponins have been reported to modulate key ferroptosis-related regulators, including the cystine/glutamate antiporter-glutathione-GPX4 axis, Nrf2 signaling, and p53-dependent pathways (Supplementary Table 1excli2026-9566_supplementary_information.pdf). For example, ginsenoside Rg3 has been shown to induce ferroptosis in hepatic stellate cells through regulation of the miR-6945-3p/DNMT3B/ACSL4 axis (Hu et al., 2024[2]), thereby alleviating liver fibrosis, and to inhibit melanoma progression by inducing ferroptosis through the p53/SLC7A11/GPX4 axis (Ma et al., 2025[5]). Similarly, saikosaponin D promotes ferroptosis in bladder cancer cells (Huang et al., 2026[3]), but alleviates ferroptosis-associated tissue injury in sepsis-induced acute lung injury through activation of Nrf2 signaling (Song et al., 2025[8]). These observations suggest that triterpenoid saponins function as context-dependent modulators rather than simple ferroptosis inducers or inhibitors. Given that ferroptosis is fundamentally linked to membrane lipid peroxidation, the membrane-active properties of saponins may explain their context-dependent effects on ferroptotic susceptibility. This observation suggests that membrane organization and the lipid microenvironment may serve as important determinants of ferroptotic sensitivity.

Declaration

Conflict of interest

The author declares no conflict of interest.

Artificial Intelligence (AI) - assisted technology

During the preparation of this manuscript, the author utilized ChatGPT (version GPT-5) for language refinement.

 

References

1. Cui S, Ye J. Ferroptosis: The Demise of Cells Through Phospholipid Peroxidation. Adv Sci. 2026;13:e24387
2. Hu Y, Lang Z, Li X, Lin L, Li Y, Zhang R, et al. Ginsenoside Rg3 promotes hepatic stellate cell ferroptosis by epigenetically regulating ACSL4 to suppress liver fibrosis progression. Phytomedicine. 2024;124:155289
3. Huang H, Guo L, Sun H, Liu Y, Zhang J, Tang W, et al. Saikosaponin D inhibits bladder cancer growth and enhances the synergistic antitumor effect of gemcitabine by targeting PI3K/AKT-mediated ferroptosis. Biochem Biophys Res Commun. 2026;816:153709
4. Li J, Cao F, Yin HL, Huang ZJ, Lin ZT, Mao N, et al. Ferroptosis: past, present and future. Cell Death Dis. 2020;11:88
5. Ma A, Zhu S, Yao X, Chen Y, Yao J, Shen M, et al. Ginsenoside Rg3 inhibits melanoma progression by inducing ferroptosis via the p53/SLC7A11/GPX4 pathway. J Adv Res. 2025:S2090-1232(25)00864-1
6. Ouyang M, Wu J, Hu X, Liu C, Zhou D. Decoding the power of saponins in ferroptosis regulation and disease intervention: a review. J Pharm Pharmacol. 2025;77:593–608
7. Podolak I, Grabowska K, Sobolewska D, Wróbel-Biedrawa D, Makowska-Wąs J, Galanty A. Saponins as cytotoxic agents: an update (2010–2021). Part II—Triterpene saponins. Phytochem Rev. 2023;22:113–167
8. Song L, Tao Y, Lu G, Wu C. Saikosaponin D ameliorates sepsis-induced acute lung injury by maintaining alveolar epithelial barrier integrity and inhibiting ferroptosis via Nrf2/HO-1 pathway. Inhal Toxicol. 2025;37:195–207
9. Yang J, Gao Y. Intercellular propagation of ferroptosis. Adv Redox Res. 2026;18:100153
10. Zhong J, Mareque-Rivas C, Lan X, Su YX. Supramolecular Assembly of Triterpenoids: Current State and Biomedical Perspectives. Aggregate. 2025;6:e70081
 
 

File-Attachments

  1. excli2026-9566_supplementary_information.pdf (377,32 KB)
    Supplementary information
 
 
 

[*] Corresponding Author:

Tae Kyung Hyun, Department of Industrial Plant Science and Technology, College of Agriculture, Life and Environment Sciences, Chungbuk National University, Cheongju 28644, Republic of Korea; Phone: +82-43-261-2520, Fax: +82-43-271-0413, eMail: taekyung7708@chungbuk.ac.kr