Cargando…
pH-Dependence Cytotoxicity Evaluation of Artepillin C against Tumor Cells
Brazilian green propolis is a well-known product that is consumed globally. Its major component, Artepillin C, showed potential as an antitumor product. This study explored the impact of Artepillin C on fibroblast and glioblastoma cell lines, used as healthy and very aggressive tumor cell lines, res...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10672498/ https://www.ncbi.nlm.nih.gov/pubmed/38004326 http://dx.doi.org/10.3390/life13112186 |
_version_ | 1785140405284634624 |
---|---|
author | Pazin, Wallance M. Miranda, Renata R. Toledo, Karina A. Kjeldsen, Frank Constantino, Carlos J. L. Brewer, Jonathan R. |
author_facet | Pazin, Wallance M. Miranda, Renata R. Toledo, Karina A. Kjeldsen, Frank Constantino, Carlos J. L. Brewer, Jonathan R. |
author_sort | Pazin, Wallance M. |
collection | PubMed |
description | Brazilian green propolis is a well-known product that is consumed globally. Its major component, Artepillin C, showed potential as an antitumor product. This study explored the impact of Artepillin C on fibroblast and glioblastoma cell lines, used as healthy and very aggressive tumor cell lines, respectively. The focus of the study was to evaluate the pH-dependence of Artepillin C cytotoxicity, since tumor cells are known to have a more acidic extracellular microenvironment compared to healthy cells, and Artepillin C was shown to become more lipophilic at lower pH values. Investigations into the pH-dependency of Artepillin C (6.0–7.4), through viability assays and live cell imaging, revealed compelling insights. At pH 6.0, MTT assays showed the pronounced cytotoxic effects of Artepillin C, yielding a notable reduction in cell viability to less than 12% among glioblastoma cells following a 24 h exposure to 100 µM of Artepillin C. Concurrently, LDH assays indicated significant membrane damage, affecting approximately 50% of the total cells under the same conditions. Our Laurdan GP analysis suggests that Artepillin C induces autophagy, and notably, provokes a lipid membrane packing effect, contributing to cell death. These combined results affirm the selective cytotoxicity of Artepillin C within the acidic tumor microenvironment, emphasizing its potential as an effective antitumor agent. Furthermore, our findings suggest that Artepillin C holds promise for potential applications in the realm of anticancer therapies given its pH-dependence cytotoxicity. |
format | Online Article Text |
id | pubmed-10672498 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-106724982023-11-09 pH-Dependence Cytotoxicity Evaluation of Artepillin C against Tumor Cells Pazin, Wallance M. Miranda, Renata R. Toledo, Karina A. Kjeldsen, Frank Constantino, Carlos J. L. Brewer, Jonathan R. Life (Basel) Article Brazilian green propolis is a well-known product that is consumed globally. Its major component, Artepillin C, showed potential as an antitumor product. This study explored the impact of Artepillin C on fibroblast and glioblastoma cell lines, used as healthy and very aggressive tumor cell lines, respectively. The focus of the study was to evaluate the pH-dependence of Artepillin C cytotoxicity, since tumor cells are known to have a more acidic extracellular microenvironment compared to healthy cells, and Artepillin C was shown to become more lipophilic at lower pH values. Investigations into the pH-dependency of Artepillin C (6.0–7.4), through viability assays and live cell imaging, revealed compelling insights. At pH 6.0, MTT assays showed the pronounced cytotoxic effects of Artepillin C, yielding a notable reduction in cell viability to less than 12% among glioblastoma cells following a 24 h exposure to 100 µM of Artepillin C. Concurrently, LDH assays indicated significant membrane damage, affecting approximately 50% of the total cells under the same conditions. Our Laurdan GP analysis suggests that Artepillin C induces autophagy, and notably, provokes a lipid membrane packing effect, contributing to cell death. These combined results affirm the selective cytotoxicity of Artepillin C within the acidic tumor microenvironment, emphasizing its potential as an effective antitumor agent. Furthermore, our findings suggest that Artepillin C holds promise for potential applications in the realm of anticancer therapies given its pH-dependence cytotoxicity. MDPI 2023-11-09 /pmc/articles/PMC10672498/ /pubmed/38004326 http://dx.doi.org/10.3390/life13112186 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Pazin, Wallance M. Miranda, Renata R. Toledo, Karina A. Kjeldsen, Frank Constantino, Carlos J. L. Brewer, Jonathan R. pH-Dependence Cytotoxicity Evaluation of Artepillin C against Tumor Cells |
title | pH-Dependence Cytotoxicity Evaluation of Artepillin C against Tumor Cells |
title_full | pH-Dependence Cytotoxicity Evaluation of Artepillin C against Tumor Cells |
title_fullStr | pH-Dependence Cytotoxicity Evaluation of Artepillin C against Tumor Cells |
title_full_unstemmed | pH-Dependence Cytotoxicity Evaluation of Artepillin C against Tumor Cells |
title_short | pH-Dependence Cytotoxicity Evaluation of Artepillin C against Tumor Cells |
title_sort | ph-dependence cytotoxicity evaluation of artepillin c against tumor cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10672498/ https://www.ncbi.nlm.nih.gov/pubmed/38004326 http://dx.doi.org/10.3390/life13112186 |
work_keys_str_mv | AT pazinwallancem phdependencecytotoxicityevaluationofartepillincagainsttumorcells AT mirandarenatar phdependencecytotoxicityevaluationofartepillincagainsttumorcells AT toledokarinaa phdependencecytotoxicityevaluationofartepillincagainsttumorcells AT kjeldsenfrank phdependencecytotoxicityevaluationofartepillincagainsttumorcells AT constantinocarlosjl phdependencecytotoxicityevaluationofartepillincagainsttumorcells AT brewerjonathanr phdependencecytotoxicityevaluationofartepillincagainsttumorcells |