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Involvement of human beta-defensin-2 in regulation of malignant potential of cultured human melanoma cells
Background and Aim: Human beta-defensin-2 (hBD-2) is an antimicrobial cationic peptide capable to control human carcinoma cell growth via cell cycle regulation. The present study was aimed on determination of hBD-2 influence on the growth patterns and malignant potential of cultured human melanoma c...
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Інститут експериментальної патології, онкології і радіобіології ім. Р.Є. Кавецького НАН України
2014
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irk-123456789-1453132019-01-21T01:23:42Z Involvement of human beta-defensin-2 in regulation of malignant potential of cultured human melanoma cells Gerashchenko, O. Zhuravel, E. Skachkova, O. Khranovska, N. Pushkarev, V. Pogrebnoy, P. Soldatkina, M. Original contributions Background and Aim: Human beta-defensin-2 (hBD-2) is an antimicrobial cationic peptide capable to control human carcinoma cell growth via cell cycle regulation. The present study was aimed on determination of hBD-2 influence on the growth patterns and malignant potential of cultured human melanoma cells. Methods: The study was performed on cultured human melanoma cells of mel Z and mel Is lines treated with recombinant hBD-2 (rec-hBD-2); cell viability, proliferation, cell cycle distribution, and anchorage-independent growth were analyzed using MTT test, direct cell counting, flow cytometry, and colony forming assay respectively. Expression and/or phosphorylation levels of proteins involved in cell cycle control were evaluated by Western blotting. Results: The treatment of mel Z and mel Is cells with rec-hBD-2 in a concentration range of 100–1000 nM resulted in a concentration-dependent suppression of cell proliferation, viability, and colony forming activity. It has been shown that rec-hBD-2 exerts its growth suppression effects via significant downregulation of B-Raf expression, activation of pRB and upregulation of p21WAF1 expression, downregulation of cyclin D1 and cyclin E resulting in cell cycle arrest at G1/S checkpoint. Conclusion: According to obtained results, hBD-2 exerts its growth suppression effect toward human melanoma cells via downregulation of B-Raf, cyclin D1 and cyclin E expression, upregulation of p21WAF1 expression and activation of pRB. Key Words: human beta-defensin-2, melanoma, proliferation, viability, cell cycle, B-Raf, anchorage-independent growth. 2014 Article Involvement of human beta-defensin-2 in regulation of malignant potential of cultured human melanoma cells / O. Gerashchenko, E. Zhuravel, O. Skachkova, N. Khranovska, V. Pushkarev, P. Pogrebnoy, M. Soldatkina // Experimental Oncology. — 2014. — Т. 36, № 1. — С. 17-23. — Бібліогр.: 35 назв. — англ. 1812-9269 http://dspace.nbuv.gov.ua/handle/123456789/145313 en Experimental Oncology Інститут експериментальної патології, онкології і радіобіології ім. Р.Є. Кавецького НАН України |
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Original contributions Original contributions Gerashchenko, O. Zhuravel, E. Skachkova, O. Khranovska, N. Pushkarev, V. Pogrebnoy, P. Soldatkina, M. Involvement of human beta-defensin-2 in regulation of malignant potential of cultured human melanoma cells Experimental Oncology |
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Background and Aim: Human beta-defensin-2 (hBD-2) is an antimicrobial cationic peptide capable to control human carcinoma cell growth via cell cycle regulation. The present study was aimed on determination of hBD-2 influence on the growth patterns and malignant potential of cultured human melanoma cells. Methods: The study was performed on cultured human melanoma cells of mel Z and mel Is lines treated with recombinant hBD-2 (rec-hBD-2); cell viability, proliferation, cell cycle distribution, and anchorage-independent growth were analyzed using MTT test, direct cell counting, flow cytometry, and colony forming assay respectively. Expression and/or phosphorylation levels of proteins involved in cell cycle control were evaluated by Western blotting. Results: The treatment of mel Z and mel Is cells with rec-hBD-2 in a concentration range of 100–1000 nM resulted in a concentration-dependent suppression of cell proliferation, viability, and colony forming activity. It has been shown that rec-hBD-2 exerts its growth suppression effects via significant downregulation of B-Raf expression, activation of pRB and upregulation of p21WAF1 expression, downregulation of cyclin D1 and cyclin E resulting in cell cycle arrest at G1/S checkpoint. Conclusion: According to obtained results, hBD-2 exerts its growth suppression effect toward human melanoma cells via downregulation of B-Raf, cyclin D1 and cyclin E expression, upregulation of p21WAF1 expression and activation of pRB. Key Words: human beta-defensin-2, melanoma, proliferation, viability, cell cycle, B-Raf, anchorage-independent growth. |
format |
Article |
author |
Gerashchenko, O. Zhuravel, E. Skachkova, O. Khranovska, N. Pushkarev, V. Pogrebnoy, P. Soldatkina, M. |
author_facet |
Gerashchenko, O. Zhuravel, E. Skachkova, O. Khranovska, N. Pushkarev, V. Pogrebnoy, P. Soldatkina, M. |
author_sort |
Gerashchenko, O. |
title |
Involvement of human beta-defensin-2 in regulation of malignant potential of cultured human melanoma cells |
title_short |
Involvement of human beta-defensin-2 in regulation of malignant potential of cultured human melanoma cells |
title_full |
Involvement of human beta-defensin-2 in regulation of malignant potential of cultured human melanoma cells |
title_fullStr |
Involvement of human beta-defensin-2 in regulation of malignant potential of cultured human melanoma cells |
title_full_unstemmed |
Involvement of human beta-defensin-2 in regulation of malignant potential of cultured human melanoma cells |
title_sort |
involvement of human beta-defensin-2 in regulation of malignant potential of cultured human melanoma cells |
publisher |
Інститут експериментальної патології, онкології і радіобіології ім. Р.Є. Кавецького НАН України |
publishDate |
2014 |
topic_facet |
Original contributions |
url |
http://dspace.nbuv.gov.ua/handle/123456789/145313 |
citation_txt |
Involvement of human beta-defensin-2 in regulation of malignant potential of cultured human melanoma cells / O. Gerashchenko, E. Zhuravel, O. Skachkova, N. Khranovska, V. Pushkarev, P. Pogrebnoy, M. Soldatkina // Experimental Oncology. — 2014. — Т. 36, № 1. — С. 17-23. — Бібліогр.: 35 назв. — англ. |
series |
Experimental Oncology |
work_keys_str_mv |
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2023-05-20T17:21:48Z |
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2023-05-20T17:21:48Z |
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