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...

Descripción completa

Detalles Bibliográficos
Autores principales: Chen, Cheng-Cheung, Hsieh, Dar-Shih, Huang, Kao-Jean, Chan, Yi-Lin, Hong, Po-Da, Yeh, Ming-Kung, Wu, Chang-Jer
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