Dergiler / Trakya University Journal of Natural Sciences / 2026 / Volume: 27 Issue: 2

In vitro anticancer effects of a marine-derived glycosaminoglycan-containing extract from Dicentrarchus labrax scales on human glioblastoma cells

Yunus Aksüt(ISTANBUL UNIVERSITY)0000-0001-9407-5019
Eren Yıldırım(ISTANBUL UNIVERSITY-CERRAHPASA)0000-0002-7924-9698
Murat Pekmez(ISTANBUL UNIVERSITY, FACULTY OF SCIENCE, DEPARTMENT OF MOLECULAR BIOLOGY AND GENETICS, MOLECULAR BIOLOGY AND GENETICS PR.)0000-0002-6150-8372
Sayfa
—
Yayın Tarihi
2026-10-15
🏛️Bu makalenin bibliyografik verileri ve tam metin bağlantısı DergiPark üzerinden sağlanmıştır.
DergiPark Kaydı ↗
✨

Yapay Zeka Hızlı Bakış & Çıkarımlar

AI Insight
⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

Although further in vivo research and compound fractionation are necessary, marine-derived GAG-rich extracts could be promising adjuncts for glioblastoma therapy.

📌 3 Maddede Bu Makale

🎯
Amaç & Hipotez:Background: Marine ecosystems are an underexplored source of structurally diverse bioactive compounds with therapeutic potential.
📊
Temel Bulgular & Veri:Aims: This study aimed to investigate the potential anticancer effects of Dicentrarchus labrax (European seabass) scale extract (DLSE) on human glioblastoma U-87MG cells.
💡
Sonuç & Katkı:Although further in vivo research and compound fractionation are necessary, marine-derived GAG-rich extracts could be promising adjuncts for glioblastoma therapy.
🔬Tür:Research Article
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Fish scale extract · marine bioactive compounds · apoptosis

Abstract

Background: Marine ecosystems are an underexplored source of structurally diverse bioactive compounds with therapeutic potential. Among these, glycosaminoglycans (GAGs) have gained attention for their anticoagulant, antioxidant, anti-inflammatory, and antitumor properties. Glioblastoma, the most aggressive malignant primary brain tumor in adults, remains largely incurable due to its high invasiveness, therapeutic resistance, and the protective blood–brain barrier. Therefore, the ongoing need to identify new treatment candidates persists. Aims: This study aimed to investigate the potential anticancer effects of Dicentrarchus labrax (European seabass) scale extract (DLSE) on human glioblastoma U-87MG cells. Methods: GAG-containing extracts were prepared from fish scales, and their chemical structures were characterized using Fourier-transform infrared (FTIR) spectroscopy. Cell viability was determined by the MTT assay, migration by scratch wound-healing assay, apoptosis by Hoechst/PI staining, and molecular changes by immunoblotting. Results: FTIR analysis confirmed the key functional groups consistent with a GAG-like polysaccharide profile. DLSE reduced cell viability in a dose- and time-dependent manner, with an IC50 value of 993 μg/mL at 72 hours. Treatments with 600 and 1000 μg/mL DLSE for 72 hours inhibited cell migration, induced apoptosis, increased the Bax/Bcl-2 ratio, and elevated levels of cleaved caspase-3 and PARP1. DLSE also activated p53/p21-mediated cell-cycle regulatory pathways, and induced ER stress through dose-dependent increases in Grp78, PERK, IRE1α, and cleaved ATF6 levels. Conclusion: Our findings indicate that GAG-containing DLSE stimulates multiple antitumor pathways in glioblastoma cells. Although further in vivo research and compound fractionation are necessary, marine-derived GAG-rich extracts could be promising adjuncts for glioblastoma therapy.

🔖

Bu Makaleye Atıf Yap

Aksüt, Y., Aksoy, N. B., Şengelen, A., Yıldırım, E., Yemişken, E., Pekmez, M. (2026). In vitro anticancer effects of a marine-derived glycosaminoglycan-containing extract from Dicentrarchus labrax scales on human glioblastoma cells. Trakya University Journal of Natural Sciences, Volume: 27 Issue: 2. https://doi.org/10.23902/trkjnat.1969474

📄 Tam Metin PDF Okuyucu

📄

PDF görüntüleyici hazırlanıyor...

Kaynakça (36)

  1. Afratis, N., Gialeli, C., Nikitovic, D., Tsegenidis, T., Karousou, E., Theocharis, A. D., Pavão, M. S., Tzanakakis, G. N., & Karamanos, N. K. (2012). Glycosaminoglycans: key players in cancer cell biology and treatment. The FEBS Journal 279(7), 1177–1197. https://doi.org/10.1111/j.1742-4658.2012.08529.x
  2. Aksüt, Y., Şengelen, A., Gürsoy, D. M., Öğütcü, İ., Kuvet, Ö., & Pekmez, M. (2025). Chrysin sensitizes glioblastoma cells and spheroids to temozolomide treatment by reducing EMT and stemness phenotypes, as well as targeting multidrug resistance proteins. Frontiers in pharmacology, 16, 1643186. https://doi.org/10.3389/fphar.2025.1643186
  3. Arvanitis, C. D., Ferraro, G. B., & Jain, R. K. (2020). The blood-brain barrier and blood-tumour barrier in brain tumours and metastases. Nature Reviews Cancer, 20(1), 26–41. https://doi.org/10.1038/s41568-019-0205-x
  4. Atashrazm, F., Lowenthal, R. M., Woods, G. M., Holloway, A. F., & Dickinson, J. L. (2015). Fucoidan and cancer: a multifunctional molecule with anti-tumor potential. Marine drugs, 13(4), 2327–2346. https://doi.org/10.3390/md13042327
  5. Augusto, A., Lemos, M. F. L., & Silva, S. F. J. (2024). Exploring Marine-Based Food Production: The Challenges for a Sustainable and Fast Biotechnology-Based Development. Applied Sciences, 14(18), 8255. https://doi.org/10.3390/app14188255
  6. Bray, F., Laversanne, M., Sung, H., Ferlay, J., Siegel, R. L., Soerjomataram, I., & Jemal, A. (2024). Global cancer statistics 2022: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA: a cancer journal for clinicians, 74(3), 229–263. https://doi.org/10.3322/caac.21834
  7. Brézillon, S., Untereiner, V., Lovergne, L., Tadeo, I., Noguera, R., Maquart, F. X., Wegrowski, Y., & Sockalingum, G. D. (2014). Glycosaminoglycan profiling in different cell types using infrared spectroscopy and imaging. Analytical and bioanalytical chemistry, 406(24), 5795–5803. https://doi.org/10.1007/s00216-014-7994-2
  8. Cabral, E. M., Mondala, J. R. M., Oliveira, M., Przyborska, J., Fitzpatrick, S., Rai, D. K., Sivagnanam, S. P., Garcia-Vaquero, M., O'Shea, D., Devereux, M., Tiwari, B. K., & Curtin, J. (2021). Influence of molecular weight fractionation on the antimicrobial and anticancer properties of a fucoidan rich-extract from the macroalgae Fucus vesiculosus. International journal of biological macromolecules, 186, 994–1002. https://doi.org/10.1016/j.ijbiomac.2021.06.182
  9. Carrasqueira, J., Bernardino, S., Bernardino, R., & Afonso, C. (2025). Marine-Derived Polysaccharides and Their Potential Health Benefits in Nutraceutical Applications. Marine drugs, 23(2). https://doi.org/10.3390/md23020060
  10. Chavante, S. F., Brito, A. S., Lima, M., Yates, E., Nader, H., Guerrini, M., Torri, G., & Bisio, A. (2014). A heparin-like glycosaminoglycan from shrimp containing high levels of 3-O-sulfated D-glucosamine groups in an unusual trisaccharide sequence. Carbohydrate research, 390, 59–66. https://doi.org/10.1016/j.carres.2014.03.002
  11. Damonte, E. B., Matulewicz, M. C., & Cerezo, A. S. (2004). Sulfated seaweed polysaccharides as antiviral agents. Current medicinal chemistry, 11(18), 2399–2419. https://doi.org/10.2174/0929867043364504
  12. de Moura, H. C., Novello, C. R., Balbinot-Alfaro, E., Düsman, E., Barddal, H. P. O., Almeida, I. V., Vicentini, V. E. P., Prentice-Hernández, C., & Alfaro, A. T. (2021). Obtaining glycosaminoglycans from tilapia (Oreochromis niloticus) scales and evaluation of its anticoagulant and cytotoxic activities: Glycosaminoglycans from tilapia scales: anticoagulant and cytotoxic activities. Food research international, 140, 110012. https://doi.org/10.1016/j.foodres.2020.110012
  13. Gerwick, W. H., & Moore, B. S. (2012). Lessons from the past and charting the future of marine natural products drug discovery and chemical biology. Chemistry & biology, 19(1), 85–98. https://doi.org/10.1016/j.chembiol.2011.12.014
  14. Grochans, S., Cybulska, A. M., Simińska, D., Korbecki, J., Kojder, K., Chlubek, D., & Baranowska-Bosiacka, I. (2022). Epidemiology of Glioblastoma Multiforme-Literature Review. Cancers (Basel), 14(10). https://doi.org/10.3390/cancers14102412
  15. Houy, N., & Le Grand, F. (2018). Administration of temozolomide: Comparison of conventional and metronomic chemotherapy regimens. Journal of theoretical biology, 446, 71–78. https://doi.org/10.1016/j.jtbi.2018.02.034
  16. Jin, J., Fang, F., Gao, W., Chen, H., Wen, J., Wen, X., & Chen, J. (2021). The Structure and Function of the Glycocalyx and Its Connection With Blood-Brain Barrier. Frontiers in cellular neuroscience, 15, 739699. https://doi.org/10.3389/fncel.2021.739699
  17. Krichen, F., Volpi, N., Sila, A., Maccari, F., Mantovani, V., Galeotti, F., Ellouz-Chaabouni, S., & Bougatef, A. (2017). Purification, structural characterization and antiproliferative properties of chondroitin sulfate/dermatan sulfate from tunisian fish skins. International journal of biological macromolecules, 95, 32–39. https://doi.org/10.1016/j.ijbiomac.2016.10.108
  18. Lettow, M., Grabarics, M., Mucha, E., Thomas, D. A., Polewski, Ł., Freyse, J., Rademann, J., Meijer, G., von Helden, G., & Pagel, K. (2020). IR action spectroscopy of glycosaminoglycan oligosaccharides. Analytical and bioanalytical chemistry, 412(3), 533–537. https://doi.org/10.1007/s00216-019-02327-7
  19. Liao, C. H., Lai, I. C., Kuo, H. C., Chuang, S. E., Lee, H. L., Whang-Peng, J., Yao, C. J., & Lai, G. M. (2019). Epigenetic Modification and Differentiation Induction of Malignant Glioma Cells by Oligo-Fucoidan. Marine drugs, 17(9). https://doi.org/10.3390/md17090525
  20. Lin, C., Zhu, X., Jin, Q., Sui, A., Li, J., & Shen, L. (2020). Effects of Holothurian Glycosaminoglycan on the Sensitivity of Lung Cancer to Chemotherapy. Integrative cancer therapies, 19, 1534735420911430. https://doi.org/10.1177/1534735420911430
  21. Lungu, A., Albu, M., Florea, N., Stancu, I., Vasile, E., & Iovu, H. (2011). The influence of glycosaminoglycan type on the collagen-glycosaminoglycan porous scaffolds. Digest Journal of Nanomaterials and Biostructures, 6(4), 1867–1875.
  22. Morla, S. (2019). Glycosaminoglycans and Glycosaminoglycan Mimetics in Cancer and Inflammation. International journal of molecular sciences, 20(8). https://doi.org/10.3390/ijms20081963
  23. Newman, D. J., & Cragg, G. M. (2020). Natural Products as Sources of New Drugs over the Nearly Four Decades from 01/1981 to 09/2019. Journal of natural products, 83(3), 770–803. https://doi.org/10.1021/acs.jnatprod.9b01285
  24. Nhani, G. B. B., Di Filippo, L. D., de Paula, G. A., Mantovanelli, V. R., da Fonseca, P. P., Tashiro, F. M., Monteiro, D. C., Fonseca-Santos, B., Duarte, J. L., & Chorilli, M. (2024). High-Tech Sustainable Beauty: Exploring Nanotechnology for the Development of Cosmetics Using Plant and Animal By-Products. Cosmetics, 11(4), 112. https://doi.org/10.3390/cosmetics11040112
  25. Pekmez, M., Mete Ş, B., Aksüt, Y., Öğütcü, İ., Baştürk, F. N., Gerçek, Y. C., & Şengelen, A. (2025). Fatty acid synthase inhibitor cerulenin attenuates glioblastoma progression by reducing EMT and stemness phenotypes, inducing oxidative and ER stress response, and targeting PI3K/AKT/NF-kB axis. Medical oncology, 42(5), 136. https://doi.org/10.1007/s12032-025-02697-2
  26. Pereira, D. M., Correia-da-Silva, G., Valentão, P., Teixeira, N., & Andrade, P. B. (2013). Palmitic acid and ergosta-7,22-dien-3-ol contribute to the apoptotic effect and cell cycle arrest of an extract from Marthasterias glacialis L. in neuroblastoma cells. Marine drugs, 12(1), 54–68. https://doi.org/10.3390/md12010054
  27. Price, M., Ballard, C., Benedetti, J., Neff, C., Cioffi, G., Waite, K. A., Kruchko, C., Barnholtz-Sloan, J. S., & Ostrom, Q. T. (2024). CBTRUS Statistical Report: Primary Brain and Other Central Nervous System Tumors Diagnosed in the United States in 2017-2021. Neuro-oncology, 26(Supplement_6), vi1–vi85. https://doi.org/10.1093/neuonc/noae145
  28. Qian, W., Tao, L., Wang, Y., Zhang, F., Li, M., Huang, S., Wang, A., Chen, W., Yue, Z., Chen, L., Liu, Y., Huang, C., Zhang, L., Li, Y., & Lu, Y. (2015). Downregulation of Integrins in Cancer Cells and Anti-Platelet Properties Are Involved in Holothurian Glycosaminoglycan-Mediated Disruption of the Interaction of Cancer Cells and Platelets in Hematogenous Metastasis. Journal of vascular research, 52(3), 197–209. https://doi.org/10.1159/000439220
  29. Ruiz-Torres, V., Forsythe, N., Pérez-Sánchez, A., Van Schaeybroeck, S., Barrajón-Catalán, E., & Micol, V. (2021). A Nudibranch Marine Extract Selectively Chemosensitizes Colorectal Cancer Cells by Inducing ROS-Mediated Endoplasmic Reticulum Stress. Frontiers in pharmacology, 12, 625946. https://doi.org/10.3389/fphar.2021.625946
  30. Singh, S., Dey, D., Barik, D., Mohapatra, I., Kim, S., Sharma, M., Prasad, S., Wang, P., Singh, A., & Singh, G. (2025). Glioblastoma at the crossroads: current understanding and future therapeutic horizons. Signal transduction and targeted therapy, 10(1), 213. https://doi.org/10.1038/s41392-025-02299-4
  31. Tan, A. C., Ashley, D. M., López, G. Y., Malinzak, M., Friedman, H. S., & Khasraw, M. (2020). Management of glioblastoma: State of the art and future directions. CA: a cancer journal for clinicians, 70(4), 299–312. https://doi.org/10.3322/caac.21613
  32. Wang, Y. N., Meng, L. H., & Wang, B. G. (2020). Progress in Research on Bioactive Secondary Metabolites from Deep-Sea Derived Microorganisms. Marine drugs, 18(12). https://doi.org/10.3390/md18120614
  33. Wen, H., Zhong, Y., Yin, Y., Qin, K., Yang, L., Li, D., Yu, W., Yang, C., Deng, Z., & Hong, K. (2022). A marine-derived small molecule induces immunogenic cell death against triple-negative breast cancer through ER stress-CHOP pathway. International journal of biological sciences, 18(7), 2898–2913. https://doi.org/10.7150/ijbs.70975
  34. Wu, R., Li, P., Wang, Y., Su, N., Xiao, M., Li, X., & Shang, N. (2022). Structural analysis and anti-cancer activity of low-molecular-weight chondroitin sulfate from hybrid sturgeon cartilage. Carbohydrate polymers, 275, 118700. https://doi.org/10.1016/j.carbpol.2021.118700
  35. Xu, K., Wang, Z., Copland, J. A., Chakrabarti, R., & Florczyk, S. J. (2020). 3D porous chitosan-chondroitin sulfate scaffolds promote epithelial to mesenchymal transition in prostate cancer cells. Biomaterials, 254, 120126. https://doi.org/10.1016/j.biomaterials.2020.120126
  36. Zahari, C., & Azmi, N.S. (2016). Halal source of medication: glycosaminoglycan derived medicinal plant. International Journal of Applied Chemistry, 12, 803–810.