Sensitization of human malignant lymphoid cells to etoposide by fucoidan, a brown seaweed polysaccharide

• Date: 2007
• Main Authors: Philchenkov, A., Zavelevich, M., Imbs, T., Zvyagintseva, T., Zaporozhets, T.
• Format: Article
• Language: English
• Published: Інститут експериментальної патології, онкології і радіобіології ім. Р.Є. Кавецького НАН України 2007
• Series: Experimental Oncology
• Subjects: Original contributions
• Online Access: https://nasplib.isofts.kiev.ua/handle/123456789/138963
• Journal Title: Digital Library of Periodicals of National Academy of Sciences of Ukraine
• Cite this: Sensitization of human malignant lymphoid cells to etoposide by fucoidan, a brown seaweed polysaccharide / A. Philchenkov, M. Zavelevich, T. Imbs, T. Zvyagintseva, T. Zaporozhets // Experimental Oncology. — 2007. — Т. 29, № 3. — С. 181-185. — Бібліогр.: 18 назв. — англ.

The search for the substances sensitizing cancer cells to apoptosis induction by chemotherapeutic agents is a task of high importance in the modern strategy of anticancer therapy. The aim of the study was to investigate the apoptogenic and apoptosis-modulating activities of fucoidan (sulfated polysaccharide) isolated from far-eastern brown seaweeds Fucus evanescens in two human malignant lymphoid cell lines, MT-4 and Namalwa. Methods: Apoptosis was assessed morphologically and quantified by flow cytometry analysis of cells stained with propidium iodide. Caspase-3 activation was assayed by flow cytometry with the aid of labeled monoclonal antibodies. Results: The fucoidan at 500 µg/ml was not cytotoxic in MT-4 or Namalwa cells even in the setting of long-term presence in culture medium up to 14 days. Nevertheless, pretreatment of MT-4 but not Namalwa cells with fucoidan followed by the exposure to DNA topoisomerase II inhibitor etoposide led to about two-fold increase in the relative apoptotic index as compared with etoposide alone. Apoptosis enhancement of MT-4 cells by fucoidan was not accompanied by further increase in the number of the cells with active form of caspase-3. Conclusion: The present findings demonstrate for the first time that fucoidan enhances etoposide induced caspase-dependent cell death pathway in MT-4 but not Namalwa cell line. The mechanisms of such enhancement do not seem to be related directly to caspase-3 activation.