Cargando…

A Novel Combination of Withaferin A and Sulforaphane Inhibits Epigenetic Machinery, Cellular Viability and Induces Apoptosis of Breast Cancer Cells

With cancer often classified as a disease that has an important epigenetic component, natural compounds that have the ability to regulate the epigenome become ideal candidates for study. Humans have a complex diet, which illustrates the need to elucidate the mechanisms of interaction between these b...

Descripción completa

Detalles Bibliográficos
Autores principales: Royston, Kendra J., Udayakumar, Neha, Lewis, Kayla, Tollefsbol, Trygve O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5455001/
https://www.ncbi.nlm.nih.gov/pubmed/28534825
http://dx.doi.org/10.3390/ijms18051092
_version_ 1783240958223056896
author Royston, Kendra J.
Udayakumar, Neha
Lewis, Kayla
Tollefsbol, Trygve O.
author_facet Royston, Kendra J.
Udayakumar, Neha
Lewis, Kayla
Tollefsbol, Trygve O.
author_sort Royston, Kendra J.
collection PubMed
description With cancer often classified as a disease that has an important epigenetic component, natural compounds that have the ability to regulate the epigenome become ideal candidates for study. Humans have a complex diet, which illustrates the need to elucidate the mechanisms of interaction between these bioactive compounds in combination. The natural compounds withaferin A (WA), from the Indian winter cherry, and sulforaphane (SFN), from cruciferous vegetables, have numerous anti-cancer effects and some report their ability to regulate epigenetic processes. Our study is the first to investigate the combinatorial effects of low physiologically achievable concentrations of WA and SFN on breast cancer cell proliferation, histone deacetylase1 (HDAC1) and DNA methyltransferases (DNMTs). No adverse effects were observed on control cells at optimal concentrations. There was synergistic inhibition of cellular viability in MCF-7 cells and a greater induction of apoptosis with the combinatorial approach than with either compound administered alone in both MDA-MB-231 and MCF-7 cells. HDAC expression was down-regulated at multiple levels. Lastly, we determined the combined effects of these bioactive compounds on the pro-apoptotic BAX and anti-apoptotic BCL-2 and found decreases in BCL-2 and increases in BAX. Taken together, our findings demonstrate the ability of low concentrations of combinatorial WA and SFN to promote cancer cell death and regulate key epigenetic modifiers in human breast cancer cells.
format Online
Article
Text
id pubmed-5455001
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-54550012017-06-08 A Novel Combination of Withaferin A and Sulforaphane Inhibits Epigenetic Machinery, Cellular Viability and Induces Apoptosis of Breast Cancer Cells Royston, Kendra J. Udayakumar, Neha Lewis, Kayla Tollefsbol, Trygve O. Int J Mol Sci Article With cancer often classified as a disease that has an important epigenetic component, natural compounds that have the ability to regulate the epigenome become ideal candidates for study. Humans have a complex diet, which illustrates the need to elucidate the mechanisms of interaction between these bioactive compounds in combination. The natural compounds withaferin A (WA), from the Indian winter cherry, and sulforaphane (SFN), from cruciferous vegetables, have numerous anti-cancer effects and some report their ability to regulate epigenetic processes. Our study is the first to investigate the combinatorial effects of low physiologically achievable concentrations of WA and SFN on breast cancer cell proliferation, histone deacetylase1 (HDAC1) and DNA methyltransferases (DNMTs). No adverse effects were observed on control cells at optimal concentrations. There was synergistic inhibition of cellular viability in MCF-7 cells and a greater induction of apoptosis with the combinatorial approach than with either compound administered alone in both MDA-MB-231 and MCF-7 cells. HDAC expression was down-regulated at multiple levels. Lastly, we determined the combined effects of these bioactive compounds on the pro-apoptotic BAX and anti-apoptotic BCL-2 and found decreases in BCL-2 and increases in BAX. Taken together, our findings demonstrate the ability of low concentrations of combinatorial WA and SFN to promote cancer cell death and regulate key epigenetic modifiers in human breast cancer cells. MDPI 2017-05-19 /pmc/articles/PMC5455001/ /pubmed/28534825 http://dx.doi.org/10.3390/ijms18051092 Text en © 2017 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Royston, Kendra J.
Udayakumar, Neha
Lewis, Kayla
Tollefsbol, Trygve O.
A Novel Combination of Withaferin A and Sulforaphane Inhibits Epigenetic Machinery, Cellular Viability and Induces Apoptosis of Breast Cancer Cells
title A Novel Combination of Withaferin A and Sulforaphane Inhibits Epigenetic Machinery, Cellular Viability and Induces Apoptosis of Breast Cancer Cells
title_full A Novel Combination of Withaferin A and Sulforaphane Inhibits Epigenetic Machinery, Cellular Viability and Induces Apoptosis of Breast Cancer Cells
title_fullStr A Novel Combination of Withaferin A and Sulforaphane Inhibits Epigenetic Machinery, Cellular Viability and Induces Apoptosis of Breast Cancer Cells
title_full_unstemmed A Novel Combination of Withaferin A and Sulforaphane Inhibits Epigenetic Machinery, Cellular Viability and Induces Apoptosis of Breast Cancer Cells
title_short A Novel Combination of Withaferin A and Sulforaphane Inhibits Epigenetic Machinery, Cellular Viability and Induces Apoptosis of Breast Cancer Cells
title_sort novel combination of withaferin a and sulforaphane inhibits epigenetic machinery, cellular viability and induces apoptosis of breast cancer cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5455001/
https://www.ncbi.nlm.nih.gov/pubmed/28534825
http://dx.doi.org/10.3390/ijms18051092
work_keys_str_mv AT roystonkendraj anovelcombinationofwithaferinaandsulforaphaneinhibitsepigeneticmachinerycellularviabilityandinducesapoptosisofbreastcancercells
AT udayakumarneha anovelcombinationofwithaferinaandsulforaphaneinhibitsepigeneticmachinerycellularviabilityandinducesapoptosisofbreastcancercells
AT lewiskayla anovelcombinationofwithaferinaandsulforaphaneinhibitsepigeneticmachinerycellularviabilityandinducesapoptosisofbreastcancercells
AT tollefsboltrygveo anovelcombinationofwithaferinaandsulforaphaneinhibitsepigeneticmachinerycellularviabilityandinducesapoptosisofbreastcancercells
AT roystonkendraj novelcombinationofwithaferinaandsulforaphaneinhibitsepigeneticmachinerycellularviabilityandinducesapoptosisofbreastcancercells
AT udayakumarneha novelcombinationofwithaferinaandsulforaphaneinhibitsepigeneticmachinerycellularviabilityandinducesapoptosisofbreastcancercells
AT lewiskayla novelcombinationofwithaferinaandsulforaphaneinhibitsepigeneticmachinerycellularviabilityandinducesapoptosisofbreastcancercells
AT tollefsboltrygveo novelcombinationofwithaferinaandsulforaphaneinhibitsepigeneticmachinerycellularviabilityandinducesapoptosisofbreastcancercells