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The effect of combination treatment of vascular endothelial growth factor receptor 3 inhibitor, MAZ-51, and zingerone on melanoma cell proliferation

Dissertation (MSc (Human Physiology))--University of Pretoria, 2024.

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Other Authors: Hlophe, Yvette Nkondo
Format: Thesis
Language:English
Published: University of Pretoria 2025
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access_status_str Open Access
author2 Hlophe, Yvette Nkondo
author_browse Hlophe, Yvette Nkondo
author_facet Hlophe, Yvette Nkondo
collection Thesis
dc_rights_str_mv © 2023 University of Pretoria. All rights reserved. The copyright in this work vests in the University of Pretoria. No part of this work may be reproduced or transmitted in any form or by any means, without the prior written permission of the University of Pretoria.
description Dissertation (MSc (Human Physiology))--University of Pretoria, 2024.
format Thesis
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institution University of Pretoria (South Africa)
language English
last_indexed 2026-06-10T12:39:19.648Z
license_str Other — see source repository
provenance_str_mv Harvested via OAI-PMH from UPSpace — University of Pretoria Institutional Repository
publishDate 2025
publishDateRange 2025
publishDateSort 2025
publisher University of Pretoria
publisherStr University of Pretoria
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source_str UPSpace — University of Pretoria Institutional Repository
spelling oai:repository.up.ac.za:2263/101485 The effect of combination treatment of vascular endothelial growth factor receptor 3 inhibitor, MAZ-51, and zingerone on melanoma cell proliferation Hlophe, Yvette Nkondo u18067507@tuks.co.za Nyakudya, Trevor Tapiwa Letsoalo, Remmotile Kganya UCTD Sustainable Development Goals (SDGs) Melanoma MAZ-51 Zingerone Chemotherapeutics Phytochemicals Dissertation (MSc (Human Physiology))--University of Pretoria, 2024. Melanoma is an aggressive form of skin cancer that is characterised by the carcinogenic transformation of melanocytes. Globally approximately 132 000 new melanoma cases are recorded annually and South Africa has recorded an incidence of 2.7 per 100 000 individuals. Various treatment strategies such as chemotherapy, targeted therapy and surgical excision are currently employed to inhibit melanoma growth, survival and progression however, the use of current treatments often results in unintended side-effects and drug resistance. Therefore, to combat this negative effect alternative treatment strategies such as medicinal plants and their bioactive phytochemicals have been widely studied and accepted as an alternative treatment, suggesting that the combined use of phytochemicals and synthetic drugs may inhibit cancer growth and proliferation with limited toxicity observed to noncancerous cells. Therefore, this study aims to investigate the individual and combined effects of (3-(4-Dimethylamino-naphthelen-1-ylmethylene)-1, 3-hydroindol-2-one) (MAZ-51) and a derivative of ginger, zingerone, on melanoma cell proliferation and survival in the melanoma (B16-F10) and human keratinocyte (HaCaT) cell lines. The cytotoxic effects of MAZ-51 (0.002-0.005 mg/mL) and zingerone (0.5-2 mg/mL) at 24, 48 and 72 hours were investigated using crystal violet assay. Additionally, crystal violet analysis was used to investigate the effects of MAZ-51 and zingerone co-treated with vascular endothelial growth factor (VEGF) on cell numbers. The morphological changes induced by the compounds were investigated using polarization optical transmitted differential contrast (PlasDIC) and hematoxylin and eosin (H&E) staining. The effects of the compounds on cell cycle progression were determined using flow cytometry. The results indicate that MAZ-51 and zingerone significantly inhibited cell growth at 48 and 72 hours (p<0.05). Morphological changes included the formation of apoptotic bodies, cellular protrusions, cell swelling and cell rounding suggesting cell death. In addition, MAZ-51 and zingerone resulted in a cell cycle block. Our findings demonstrate that MAZ-51 and zingerone exhibit significant antiproliferative effects on melanoma cells, with zingerone showing potential in reducing melanoma cell viability. National Research Foundation Physiology MSc (Human Physiology) Unrestricted Faculty of Health Sciences SDG-03:Good heatlh and well-being SDG-08:Decent work and economic growth SDG-09: Industry, innovation and infrastructure 2025-03-13T13:18:54Z 2025-03-13T13:18:54Z 2025-04 2024-12 Dissertation * A2025 http://hdl.handle.net/2263/101485 DOI: https://doi.org/10.25403/UPresearchdata.28585634.v1 https://doi.org/10.25403/UPresearchdata.28585634 en © 2023 University of Pretoria. All rights reserved. The copyright in this work vests in the University of Pretoria. No part of this work may be reproduced or transmitted in any form or by any means, without the prior written permission of the University of Pretoria. application/pdf University of Pretoria
spellingShingle UCTD
Sustainable Development Goals (SDGs)
Melanoma
MAZ-51
Zingerone
Chemotherapeutics
Phytochemicals
The effect of combination treatment of vascular endothelial growth factor receptor 3 inhibitor, MAZ-51, and zingerone on melanoma cell proliferation
title The effect of combination treatment of vascular endothelial growth factor receptor 3 inhibitor, MAZ-51, and zingerone on melanoma cell proliferation
title_full The effect of combination treatment of vascular endothelial growth factor receptor 3 inhibitor, MAZ-51, and zingerone on melanoma cell proliferation
title_fullStr The effect of combination treatment of vascular endothelial growth factor receptor 3 inhibitor, MAZ-51, and zingerone on melanoma cell proliferation
title_full_unstemmed The effect of combination treatment of vascular endothelial growth factor receptor 3 inhibitor, MAZ-51, and zingerone on melanoma cell proliferation
title_short The effect of combination treatment of vascular endothelial growth factor receptor 3 inhibitor, MAZ-51, and zingerone on melanoma cell proliferation
title_sort effect of combination treatment of vascular endothelial growth factor receptor 3 inhibitor maz 51 and zingerone on melanoma cell proliferation
topic UCTD
Sustainable Development Goals (SDGs)
Melanoma
MAZ-51
Zingerone
Chemotherapeutics
Phytochemicals
url http://hdl.handle.net/2263/101485
https://doi.org/10.25403/UPresearchdata.28585634