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Growth inhibitory activity of Ankaferd hemostat on primary melanoma cells and cell lines

OBJECTIVE: Ankaferd hemostat is the first topical hemostatic agent about the red blood cell–fibrinogen relations tested in the clinical trials. Ankaferd hemostat consists of standardized plant extracts including Alpinia officinarum, Glycyrrhiza glabra, Thymus vulgaris, Urtica dioica, and Vitis vinif...

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Autores principales: Turk, Seyhan, Malkan, Umit Yavuz, Ghasemi, Mehdi, Hocaoglu, Helin, Mutlu, Duygu, Gunes, Gursel, Aksu, Salih, Haznedaroglu, Ibrahim Celalettin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5336193/
https://www.ncbi.nlm.nih.gov/pubmed/28293423
http://dx.doi.org/10.1177/2050312116689519
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author Turk, Seyhan
Malkan, Umit Yavuz
Ghasemi, Mehdi
Hocaoglu, Helin
Mutlu, Duygu
Gunes, Gursel
Aksu, Salih
Haznedaroglu, Ibrahim Celalettin
author_facet Turk, Seyhan
Malkan, Umit Yavuz
Ghasemi, Mehdi
Hocaoglu, Helin
Mutlu, Duygu
Gunes, Gursel
Aksu, Salih
Haznedaroglu, Ibrahim Celalettin
author_sort Turk, Seyhan
collection PubMed
description OBJECTIVE: Ankaferd hemostat is the first topical hemostatic agent about the red blood cell–fibrinogen relations tested in the clinical trials. Ankaferd hemostat consists of standardized plant extracts including Alpinia officinarum, Glycyrrhiza glabra, Thymus vulgaris, Urtica dioica, and Vitis vinifera. The aim of this study was to determine the effect of Ankaferd hemostat on viability of melanoma cell lines. METHODS: Dissimilar melanoma cell lines and primary cells were used in this study. These cells were treated with different concentrations of Ankaferd hemostat to assess the impact of different dosages of the drug. All cells treated with different concentrations were incubated for different time intervals. After the data had been obtained, one-tailed T-test was used to determine whether the Ankaferd hemostat would have any significant inhibitory impact on cell growth. RESULTS: We demonstrated in this study that cells treated with Ankaferd hemostat showed a significant decrease in cell viability compared to control groups. The cells showed different resistances against Ankaferd hemostat which depended on the dosage applied and the time treated cells had been incubated. We also demonstrated an inverse relationship between the concentration of the drug and the incubation time on one hand and the viability of the cells on the other hand, that is, increasing the concentration of the drug and the incubation time had a negative impact on cell viability. CONCLUSION: The findings in our study contribute to our knowledge about the anticancer impact of Ankaferd hemostat on different melanoma cells.
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spelling pubmed-53361932017-03-14 Growth inhibitory activity of Ankaferd hemostat on primary melanoma cells and cell lines Turk, Seyhan Malkan, Umit Yavuz Ghasemi, Mehdi Hocaoglu, Helin Mutlu, Duygu Gunes, Gursel Aksu, Salih Haznedaroglu, Ibrahim Celalettin SAGE Open Med Original Article OBJECTIVE: Ankaferd hemostat is the first topical hemostatic agent about the red blood cell–fibrinogen relations tested in the clinical trials. Ankaferd hemostat consists of standardized plant extracts including Alpinia officinarum, Glycyrrhiza glabra, Thymus vulgaris, Urtica dioica, and Vitis vinifera. The aim of this study was to determine the effect of Ankaferd hemostat on viability of melanoma cell lines. METHODS: Dissimilar melanoma cell lines and primary cells were used in this study. These cells were treated with different concentrations of Ankaferd hemostat to assess the impact of different dosages of the drug. All cells treated with different concentrations were incubated for different time intervals. After the data had been obtained, one-tailed T-test was used to determine whether the Ankaferd hemostat would have any significant inhibitory impact on cell growth. RESULTS: We demonstrated in this study that cells treated with Ankaferd hemostat showed a significant decrease in cell viability compared to control groups. The cells showed different resistances against Ankaferd hemostat which depended on the dosage applied and the time treated cells had been incubated. We also demonstrated an inverse relationship between the concentration of the drug and the incubation time on one hand and the viability of the cells on the other hand, that is, increasing the concentration of the drug and the incubation time had a negative impact on cell viability. CONCLUSION: The findings in our study contribute to our knowledge about the anticancer impact of Ankaferd hemostat on different melanoma cells. SAGE Publications 2017-02-10 /pmc/articles/PMC5336193/ /pubmed/28293423 http://dx.doi.org/10.1177/2050312116689519 Text en © The Author(s) 2017 http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License (http://www.creativecommons.org/licenses/by-nc/3.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page(https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Article
Turk, Seyhan
Malkan, Umit Yavuz
Ghasemi, Mehdi
Hocaoglu, Helin
Mutlu, Duygu
Gunes, Gursel
Aksu, Salih
Haznedaroglu, Ibrahim Celalettin
Growth inhibitory activity of Ankaferd hemostat on primary melanoma cells and cell lines
title Growth inhibitory activity of Ankaferd hemostat on primary melanoma cells and cell lines
title_full Growth inhibitory activity of Ankaferd hemostat on primary melanoma cells and cell lines
title_fullStr Growth inhibitory activity of Ankaferd hemostat on primary melanoma cells and cell lines
title_full_unstemmed Growth inhibitory activity of Ankaferd hemostat on primary melanoma cells and cell lines
title_short Growth inhibitory activity of Ankaferd hemostat on primary melanoma cells and cell lines
title_sort growth inhibitory activity of ankaferd hemostat on primary melanoma cells and cell lines
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5336193/
https://www.ncbi.nlm.nih.gov/pubmed/28293423
http://dx.doi.org/10.1177/2050312116689519
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