Cargando…
Improving anticancer efficacy of (–)-epigallocatechin-3-gallate gold nanoparticles in murine B16F10 melanoma cells
(–)-Epigallocatechin-3-gallate (EGCG), the major bioactive constituent in green tea, has been reported to effectively inhibit the formation and development of tumors. To maximize the effectiveness of EGCG, we attached it to nanogold particles (EGCG-pNG) in various ratios to examine in vitro cytotoxi...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4020885/ https://www.ncbi.nlm.nih.gov/pubmed/24855338 http://dx.doi.org/10.2147/DDDT.S58414 |
_version_ | 1782316145420795904 |
---|---|
author | Chen, Cheng-Cheung Hsieh, Dar-Shih Huang, Kao-Jean Chan, Yi-Lin Hong, Po-Da Yeh, Ming-Kung Wu, Chang-Jer |
author_facet | Chen, Cheng-Cheung Hsieh, Dar-Shih Huang, Kao-Jean Chan, Yi-Lin Hong, Po-Da Yeh, Ming-Kung Wu, Chang-Jer |
author_sort | Chen, Cheng-Cheung |
collection | PubMed |
description | (–)-Epigallocatechin-3-gallate (EGCG), the major bioactive constituent in green tea, has been reported to effectively inhibit the formation and development of tumors. To maximize the effectiveness of EGCG, we attached it to nanogold particles (EGCG-pNG) in various ratios to examine in vitro cytotoxicity and in vivo anti-cancer activity. EGCG-pNG showed improved anti-cancer efficacy in B16F10 murine melanoma cells; the cytotoxic effect in the melanoma cells treated with EGCG-pNG was 4.91 times higher than those treated with EGCG. The enhancement is achieved through mitochondrial pathway-mediated apoptosis as determined by annexin V assay, JC-10 staining, and caspase-3, -8, -9 activity assay. Moreover, EGCG-pNG was 1.66 times more potent than EGCG for inhibition of tumor growth in a murine melanoma model. In the hemolysis assay, the pNG surface conjugated with EGCG is most likely the key factor that contributes to the decreased release of hemoglobin from human red blood cells. |
format | Online Article Text |
id | pubmed-4020885 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-40208852014-05-22 Improving anticancer efficacy of (–)-epigallocatechin-3-gallate gold nanoparticles in murine B16F10 melanoma cells Chen, Cheng-Cheung Hsieh, Dar-Shih Huang, Kao-Jean Chan, Yi-Lin Hong, Po-Da Yeh, Ming-Kung Wu, Chang-Jer Drug Des Devel Ther Original Research (–)-Epigallocatechin-3-gallate (EGCG), the major bioactive constituent in green tea, has been reported to effectively inhibit the formation and development of tumors. To maximize the effectiveness of EGCG, we attached it to nanogold particles (EGCG-pNG) in various ratios to examine in vitro cytotoxicity and in vivo anti-cancer activity. EGCG-pNG showed improved anti-cancer efficacy in B16F10 murine melanoma cells; the cytotoxic effect in the melanoma cells treated with EGCG-pNG was 4.91 times higher than those treated with EGCG. The enhancement is achieved through mitochondrial pathway-mediated apoptosis as determined by annexin V assay, JC-10 staining, and caspase-3, -8, -9 activity assay. Moreover, EGCG-pNG was 1.66 times more potent than EGCG for inhibition of tumor growth in a murine melanoma model. In the hemolysis assay, the pNG surface conjugated with EGCG is most likely the key factor that contributes to the decreased release of hemoglobin from human red blood cells. Dove Medical Press 2014-05-08 /pmc/articles/PMC4020885/ /pubmed/24855338 http://dx.doi.org/10.2147/DDDT.S58414 Text en © 2014 Chen et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Chen, Cheng-Cheung Hsieh, Dar-Shih Huang, Kao-Jean Chan, Yi-Lin Hong, Po-Da Yeh, Ming-Kung Wu, Chang-Jer Improving anticancer efficacy of (–)-epigallocatechin-3-gallate gold nanoparticles in murine B16F10 melanoma cells |
title | Improving anticancer efficacy of (–)-epigallocatechin-3-gallate gold nanoparticles in murine B16F10 melanoma cells |
title_full | Improving anticancer efficacy of (–)-epigallocatechin-3-gallate gold nanoparticles in murine B16F10 melanoma cells |
title_fullStr | Improving anticancer efficacy of (–)-epigallocatechin-3-gallate gold nanoparticles in murine B16F10 melanoma cells |
title_full_unstemmed | Improving anticancer efficacy of (–)-epigallocatechin-3-gallate gold nanoparticles in murine B16F10 melanoma cells |
title_short | Improving anticancer efficacy of (–)-epigallocatechin-3-gallate gold nanoparticles in murine B16F10 melanoma cells |
title_sort | improving anticancer efficacy of (–)-epigallocatechin-3-gallate gold nanoparticles in murine b16f10 melanoma cells |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4020885/ https://www.ncbi.nlm.nih.gov/pubmed/24855338 http://dx.doi.org/10.2147/DDDT.S58414 |
work_keys_str_mv | AT chenchengcheung improvinganticancerefficacyofepigallocatechin3gallategoldnanoparticlesinmurineb16f10melanomacells AT hsiehdarshih improvinganticancerefficacyofepigallocatechin3gallategoldnanoparticlesinmurineb16f10melanomacells AT huangkaojean improvinganticancerefficacyofepigallocatechin3gallategoldnanoparticlesinmurineb16f10melanomacells AT chanyilin improvinganticancerefficacyofepigallocatechin3gallategoldnanoparticlesinmurineb16f10melanomacells AT hongpoda improvinganticancerefficacyofepigallocatechin3gallategoldnanoparticlesinmurineb16f10melanomacells AT yehmingkung improvinganticancerefficacyofepigallocatechin3gallategoldnanoparticlesinmurineb16f10melanomacells AT wuchangjer improvinganticancerefficacyofepigallocatechin3gallategoldnanoparticlesinmurineb16f10melanomacells |