Journals / Osmangazi Tıp Dergisi / 2026 / Cilt: 48 Sayı: 3

Effect of Iturin A on Oxidative Stress and Immune Response in Breast Cancer Cell Lines

İturin A’nın Meme Kanseri Hücre Hatlarında Oksidatif Stres Üzerine Etkisi

Pınar Altın Çelik(ERCİYES ÜNİVERSİTESİ, TIP FAKÜLTESİ)0000-0001-8429-009X
Hamiyet Eciroğlu(ALANYA ÜNİVERSİTESİ, MESLEK YÜKSEKOKULU)0000-0002-3555-3946
Pages
501–507
Publication Date
2026-05-12
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

These findings suggest that Iturin A could be a potential agent targeting redox and inflammation balance in breast cancer therapy.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:This study aimed to evaluate the effects of Iturin A on oxidative stress and DNA damage, and immune response in MCF-7 and MDA-MB-231 breast cancer cells.
📊
Key Findings & Data:Total antioxidant capacity (TAC), total oxidant status (TOS), and 8-hydroxy-2′-deoxiguanosine (8-OHdG) levels were determined by spectrophotometric and ELISA methods, oxidative stress index (OSI) was calculated.
💡
Conclusion & Impact:These findings suggest that Iturin A could be a potential agent targeting redox and inflammation balance in breast cancer therapy.
🔬Design:Araştırma Makalesi
📍Scope:Comprehensive Sample
⚙️Variables:Iturin A · Oksidatif stres · Meme kanseri

Abstract

This study aimed to evaluate the effects of Iturin A on oxidative stress and DNA damage, and immune response in MCF-7 and MDA-MB-231 breast cancer cells. Total antioxidant capacity (TAC), total oxidant status (TOS), and 8-hydroxy-2′-deoxiguanosine (8-OHdG) levels were determined by spectrophotometric and ELISA methods, oxidative stress index (OSI) was calculated. NF-κB and COX-2 gene expression levels were analyzed using RT-qPCR. Iturin A significantly increased TAC (p<0.0001 in both), TOS (p<0.0001 in both), and 8-OHdG (p<0.01 and p<0.001, respectively) levels in both MCF-7 and MDA-MB-231 cells. Iturin A treatment significantly increased OSI levels in MCF-7 cells (p<0.001), although an increase in MDA-MB-231 cells was not statistically significant (p>0.05). Iturin A treatment significantly reduced NF-κB expression in MCF-7 cells (p<0.0001) and MDA-MB-231 (p<0.05) cells. But, the observed changes in COX-2 gene expression were not statistically significant in either cell line (p>0.05). Iturin A may differentially modulate oxidative balance and immune response in estrogen receptor-positive and -negative breast cancer cells. These findings suggest that Iturin A could be a potential agent targeting redox and inflammation balance in breast cancer therapy.

Özet

Bu çalışma, Iturin A’nın MCF-7 ve MDA-MB-231 meme kanseri hücrelerinde oksidatif stres DNA hasarı ve immün yanıt etkilerini değerlendirmek amacıyla yapılmıştır. Hücrelerde toplam antioksidan kapasite (TAK), toplam oksidan statüsü (TOS) ve 8-hidroksi-2′-deoksiguanozin (8-OHdG) seviyeleri spektrofotometre ve ELISA yöntemleriyle ölçülmüş ve oksidatif stres indeksi (OSI) hesaplanmıştır. NF-κB ve COX-2 gen ekspresyon düzeyleri RT-qPCR yöntemiyle analiz edilmiştir. Iturin A, hem MCF-7 hücrelerinde hem de MDA-MB-231 hücrelerinde. TAK (her ikisinde de p<0,0001), TOS (her ikisinde de p<0,0001) ve 8-OHdG (sırasıyla, p<0,01 ve p<0,001) düzeylerini önemli ölçüde artırmıştır. Iturin A, MCF-7 hücrelerinde OSI (p<0,001) düzeylerinde istatistiksel olarak anlamlı artışa yol açarken, MDA-MB-231 hücrelerinde istatistiksel olarak anlamlı artışa neden olmamıştır (p>0,05). Iturin A tedavisi, MCF-7 (p<0,0001) ve MDA-MB-231 (p<0,05) hücrelerinde NF-κB ekspresyonunu önemli ölçüde azaltmıştır. Ancak, COX-2 gen ekspresyonunda gözlenen değişimler, her iki hücre hattında da istatistiksel olarak anlamlı bulunmamıştır (p>0,05). Iturin A, östrojen reseptörü pozitif ve negatif meme kanseri hücrelerinde oksidatif denge ve immün yanıtı farklı biçimlerde modüle edebilir. Bu bulgular, Iturin A’nın meme kanseri tedavisinde redoks ve inflamasyon dengesini hedef alan potansiyel bir ajan olabileceğini göstermektedir.

🔖

Cite This Article

Çelik, P. A., Andeden, M. D., Eciroğlu, H., Altuntaş, H. D. (2026). Effect of Iturin A on Oxidative Stress and Immune Response in Breast Cancer Cell Lines. Osmangazi Tıp Dergisi, Cilt: 48 Sayı: 3, 501–507. https://doi.org/10.20515/otd.1819286

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (32)

  1. Arnold M, Morgan E, Rumgay H, Mafra A, Singh D, Laversanne M, et al. Current and future burden of breast cancer: Global statistics for 2020 and 2040. The Breast: Official Journal of the European Society of Mastology. 2022;66:15-23.
  2. Mota A de L, Evangelista AF, Macedo T, Oliveira R, Scapulatempo-Neto C, Vieira RA da C, et al. Molecular characterization of breast cancer cell lines by clinical immunohistochemical markers. Oncol Lett. 2017;13(6):470812.
  3. Horwitz KB, Costlow ME, McGuire WL. MCF-7; a human breast cancer cell line with estrogen, androgen, progesterone, and glucocorticoid receptors. Steroids. 1975;26(6):785–95.
  4. Derya-Andeden M, Altın-Çelik P, Andeden EE, Öztürk Ş, Dönmez-Altuntaş H. Antioxidant capacity, total phenolic content, and in vitro cytotoxic and oxidative effects of the methanol extract of Dunaliella sp. against breast cancer cells. International Journal of Secondary Metabolite. 2025;12(3):537–47.
  5. Derya-Andeden M, Altın-Çelik P, Çakır M, Üzen R, Dönmez-Altuntaş H. Effects of Pervari Honey from Türkiye on Proliferation, Oxidative Stress, and Apoptosis of Human Breast Cancer Cells. Journal of Advanced Research in Natural and Applied Sciences. 2024;10(3):627–39.
  6. Singh P, Cameotra SS. Potential applications of microbial surfactants in biomedical sciences. Trends Biotechnol. 2004;22(3):142–6.
  7. Altin-Celik P, Eken A, Derya-Andeden M, Eciroglu H, Uzen R, Donmez-Altuntas H. Iturin A and Gramicidin A inhibit proliferation, trigger apoptosis, and regulate inflammation in breast cancer cells. J Drug Deliv Sci Technol. 2024;100:106121.
  8. Çelik PA, Andeden MD, Altuntaş H. Anti-inflammatory effects of Iturin A on the 6-OHDA-induced SH-SY5Y cell model of Parkinson’s disease. Ege Journal of Medicine. 2025;64(2):193–200.
  9. Zhao H, Xu X, Lei S, Shao D, Jiang C, Shi J, et al. Iturin A-like lipopeptides from Bacillus subtilis trigger apoptosis, paraptosis, and autophagy in Caco-2 cells. J Cell Physiol. 2019;234(5):6414–27.
  10. Zhao H, Zhao X, Lei S, Zhang Y, Shao D, Jiang C, et al. Effect of cell culture models on the evaluation of anticancer activity and mechanism analysis of the potential bioactive compound, iturin A, produced by: Bacillus subtilis. Food Funct. 2019;10(3):1478–89.
  11. Pan H, Zhao X, Gao Z, Qi G. A Surfactin Lipopeptide Adjuvanted Hepatitis B Vaccines Elicit Enhanced Humoral and Cellular Immune Responses in Mice. Protein Pept Lett. 2014;21(9):901–10.
  12. Zhao H, Li J, Zhang Y, Lei S, Zhao X, Shao D, et al. Potential of iturins as functional agents: Safe, probiotic, and cytotoxic to cancer cells. Food Funct. 2018;9(11):5580–7.
  13. Ismail PA, Ali LM, Fattah CN. Associated alterations of protein oxidation and cytokines levels in breast cancer. Zagazig University Medical Journal. 2025;31(2):729–38.
  14. Pilger A, Rüdiger HW. 8-Hydroxy-2’-deoxyguanosine as a marker of oxidative DNA damage related to occupational and environmental exposures. Int Arch Occup Environ Health. 2006;80(1):1–15.
  15. Zhang T, Andrukhov O, Haririan H, Müller-Kern M, Liu S, Liu Z, et al. Total Antioxidant Capacity and Total Oxidant Status in Saliva of Periodontitis Patients in Relation to Bacterial Load. Front Cell Infect Microbiol. 2016;5:97-107.
  16. Karkhanei B, Talebi Ghane E, Mehri F. Evaluation of oxidative stress level: total antioxidant capacity, total oxidant status and glutathione activity in patients with COVID-19. New Microbes New Infect. 2021;42.
  17. Szweda M, Rychlik A, Babińska I, Pomianowski A. Significance of Cyclooxygenase-2 in Oncogenesis. J Vet Res. 2019;63(2):215.
  18. Joo Weon Lim, Kim H, Kyung Hwan Kim. Nuclear factor-kappaB regulates cyclooxygenase-2 expression and cell proliferation in human gastric cancer cells. Lab Invest. 2001;81(3):349–60.
  19. Park MH, Hong JT. Roles of NF-κB in Cancer and Inflammatory Diseases and Their Therapeutic Approaches. Cells. 2016;29;5(2):15.
  20. Janion K, Strzelczyk JK, Walkiewicz KW, Biernacki K, Copija A, Szczepańska E, et al. Evaluation of Malondialdehyde Level, Total Oxidant/Antioxidant Status and Oxidative Stress Index in Colorectal Cancer Patients. Metabolites. 2022;12(11).
  21. Karihtala P, Kauppila S, Puistola U, Jukkola-Vuorinen A. Divergent behaviour of oxidative stress markers 8-hydroxydeoxyguanosine (8-OHdG) and 4-hydroxy-2-nonenal (HNE) in breast carcinogenesis. Histopathology. 2011;58(6):854–62.
  22. Li D, Zhang W, Zhu J, Chang P, Sahin A, Singletary E, et al. Oxidative DNA damage and 8-hydroxy-2-deoxyguanosine DNA glycosylase/apurinic lyase in human breast cancer. Mol Carcinog. 2001;31(4):214–23.
  23. Valavanidis A, Vlachogianni T, Fiotakis C. 8-hydroxy-2’ -deoxyguanosine (8-OHdG): A critical biomarker of oxidative stress and carcinogenesis. J Environ Sci Health C Environ Carcinog Ecotoxicol Rev. 2009;27(2):120–39.
  24. Panis C, Victorino VJ, Herrera ACSA, Freitas LF, De Rossi T, Campos FC, et al. Differential oxidative status and immune characterization of the early and advanced stages of human breast cancer. Breast Cancer Res Treat. 2012;133(3):881–8.
  25. Morgan MJ, Liu ZG. Crosstalk of reactive oxygen species and NF-κB signaling. Cell Research. 2010;21(1):103–15.
  26. García-Sánchez A, Miranda-Díaz AG, Cardona-Muñoz EG. The Role of Oxidative Stress in Physiopathology and Pharmacological Treatment with Pro- and Antioxidant Properties in Chronic Diseases. Oxid Med Cell Longev. 2020;2020:2082145.
  27. Eynde J Vanden, Sezer F, Deniz S, Dubey A, Sharma B. Targeting Oxidative Stress Biomarkers in Breast Cancer Development and the Potential Protective Effect of Phytochemicals. Drugs and Drug Candidates. 2025;4(2):23.
  28. Reuter S, Gupta SC, Chaturvedi MM, Aggarwal BB. Oxidative stress, inflammation, and cancer: How are they linked? Free Radic Biol Med. 2010;49(11):1603–16.
  29. Schmitz KJ, Callies R, Wohlschlaeger J, Kimmig R, Otterbach F, Bohr J, et al. Overexpression of cyclo‐oxygenase‐2 is an independent predictor of unfavourable outcome in node‐negative breast cancer, but is not associated with protein kinase B (Akt) and mitogen‐activated protein kinase (ERK1/2, p38) activation or with Her‐2/neu signalling pathways. J Clin Pathol. 2006;59(7):685.
  30. Howe LR. Inflammation and breast cancer. Cyclooxygenase/prostaglandin signaling and breast cancer. Breast Cancer Res. 2007;9(4).
  31. Zhao H, Yan L, Xu X, Jiang C, Shi J, Zhang Y, et al. Potential of Bacillus subtilis lipopeptides in anti-cancer I: induction of apoptosis and paraptosis and inhibition of autophagy in K562 cells. AMB Express. 2018;8(1):78.
  32. Arnold M, Morgan E, Rumgay H, Mafra A, Singh D, Laversanne M, et al. Current and future burden of breast cancer: Global statistics for 2020 and 2040. The Breast: Official Journal of the European Society of Mastology. 2022;66:15-23.