Pro-oxidant effect of lobaric acid as a therapeutic strategy against breast cancer: a molecular perspective

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Özet

Background: This study aimed to investigate the anticancer effects of lobaric acid (LA), a lichen acid, in MCF-7 cells. Our previous study demonstrated that LA exhibits anticancer effects by triggering apoptosis in MCF-7 cells. However, the relationship between this anticancer effect and the oxidative pathway and apoptosis mechanism has not been explained. In this study, the cytotoxic and anticancer effects of LA on MCF-7 cells were investigated through oxidative stress and thioredoxin system pathways. Methods and results: For this purpose, reactive oxygen species (ROS), reduced glutathione (GSH), and malondialdehyde (MDA) levels were measured in MCF-7 cells exposed to LA at a concentration of 44.21 µg/mL (IC50). Additionally, the activities, gene, and protein levels of SOD, CAT, GPx, GST, GR, and TrxR enzymes were evaluated. In addition, the expression levels of TXN and TXNIP genes were also analyzed. The results showed that LA increased ROS and MDA levels and decreased GSH levels. Antioxidant enzyme activities (SOD, CAT, GR, TrxR) and protein levels decreased compared to the control, while heterogeneous changes were observed in gene expression levels. Despite increased GPX gene expression, a decrease in enzyme activity and protein levels was observed. While no change in TXN gene expression was observed, protein levels were decreased. TXNIP protein levels were also decreased. Conclusions: The findings provide important data for evaluating lichen-derived compounds as potential anticancer agents targeting redox balance. © The Author(s), under exclusive licence to Springer Nature B.V. 2026.

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RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/10058Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1007/s11033-026-11688-zYayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorToraman, Emine
dc.contributor.authorKalın, Şeyda Nur
dc.contributor.authorBayındırlı, Kübra Nur
dc.contributor.authorGünaydın, Şükran
dc.contributor.authorKeleş, Fatmanur
dc.contributor.authorAltay, Ahmet
dc.contributor.authorBudak, Harun
dc.date.accessioned2026-10-18T20:25:18.457672606Z
dc.date.available2026-10-18T20:25:18.457672606Z
dc.date.issued2026
dc.description.abstractBackground: This study aimed to investigate the anticancer effects of lobaric acid (LA), a lichen acid, in MCF-7 cells. Our previous study demonstrated that LA exhibits anticancer effects by triggering apoptosis in MCF-7 cells. However, the relationship between this anticancer effect and the oxidative pathway and apoptosis mechanism has not been explained. In this study, the cytotoxic and anticancer effects of LA on MCF-7 cells were investigated through oxidative stress and thioredoxin system pathways. Methods and results: For this purpose, reactive oxygen species (ROS), reduced glutathione (GSH), and malondialdehyde (MDA) levels were measured in MCF-7 cells exposed to LA at a concentration of 44.21 µg/mL (IC50). Additionally, the activities, gene, and protein levels of SOD, CAT, GPx, GST, GR, and TrxR enzymes were evaluated. In addition, the expression levels of TXN and TXNIP genes were also analyzed. The results showed that LA increased ROS and MDA levels and decreased GSH levels. Antioxidant enzyme activities (SOD, CAT, GR, TrxR) and protein levels decreased compared to the control, while heterogeneous changes were observed in gene expression levels. Despite increased GPX gene expression, a decrease in enzyme activity and protein levels was observed. While no change in TXN gene expression was observed, protein levels were decreased. TXNIP protein levels were also decreased. Conclusions: The findings provide important data for evaluating lichen-derived compounds as potential anticancer agents targeting redox balance. © The Author(s), under exclusive licence to Springer Nature B.V. 2026.
dc.description.sponsorshipThis work was supported by T\u00DCB\u0130TAK 1002 projects. Project No: 119Z112.
dc.identifier.doi10.1007/s11033-026-11688-z
dc.identifier.eissn1573-4978
dc.identifier.issn0301-4851
dc.identifier.issue1
dc.identifier.pmid41854754
dc.identifier.scopus2-s2.0-105033854085
dc.identifier.startpage520
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/10058
dc.identifier.volume53
dc.identifier.wosWOS:001719147100001
dc.language.isoen
dc.publisherSpringer Science and Business Media B.V.
dc.relation.ispartofMolecular Biology Reports
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectLobaric acid
dc.subjectMCF-7
dc.subjectOxidative stress
dc.subjectThioredoxin system
dc.subjectAntineoplastic Agents
dc.subjectAntioxidants
dc.subjectApoptosis
dc.subjectBreast Neoplasms
dc.subjectFemale
dc.subjectGlutathione
dc.subjectHumans
dc.subjectMalondialdehyde
dc.subjectMCF-7 Cells
dc.subjectReactive Oxygen Species
dc.subjectThioredoxins
dc.subjectantineoplastic agent
dc.subjectantioxidant
dc.subjectbeta actin
dc.subjectcatalase
dc.subjectcopper zinc superoxide dismutase
dc.subjectglutathione peroxidase
dc.subjectglutathione reductase
dc.subjectglutathione transferase
dc.subjectmalonaldehyde
dc.subjectphenol derivative
dc.subjectreactive oxygen metabolite
dc.subjectsuperoxide dismutase
dc.subjectthioredoxin
dc.subjectthioredoxin interacting protein
dc.subjectthioredoxin reductase
dc.titlePro-oxidant effect of lobaric acid as a therapeutic strategy against breast cancer: a molecular perspective
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus2
rdl.citation.wos2
rdl.departmentFaculty of Science and Arts, Department of Chemistry, Erzincan Binali Yıldırım University, Erzincan, 24002, Turkey. | Faculty of Science and Arts, Department of Chemistry, Erzincan Binali Yıldırım University, Erzincan, 24002, Turkey. aaltay@erzincan.edu.tr.
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)