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Sulforaphane, a natural component of broccoli, inhibits vestibular schwannoma growth in vitro and in vivo

Vestibular schwannoma (VS) is an intracranial tumor that causes significant morbidity, including hearing loss, tinnitus, dizziness, and possibly even death from brainstem compression. However, FDA-approved pharmacologic treatments for VS do not exist. Sulforaphane (SFN) is a naturally occurring isot...

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Autores principales: Kim, Bo Gyung, Fujita, Takeshi, Stankovic, Konstantina M., Welling, D. Bradley, Moon, In Seok, Choi, Jae Young, Yun, Jieun, Kang, Jong Soon, Lee, Jong Dae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5090244/
https://www.ncbi.nlm.nih.gov/pubmed/27805058
http://dx.doi.org/10.1038/srep36215
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author Kim, Bo Gyung
Fujita, Takeshi
Stankovic, Konstantina M.
Welling, D. Bradley
Moon, In Seok
Choi, Jae Young
Yun, Jieun
Kang, Jong Soon
Lee, Jong Dae
author_facet Kim, Bo Gyung
Fujita, Takeshi
Stankovic, Konstantina M.
Welling, D. Bradley
Moon, In Seok
Choi, Jae Young
Yun, Jieun
Kang, Jong Soon
Lee, Jong Dae
author_sort Kim, Bo Gyung
collection PubMed
description Vestibular schwannoma (VS) is an intracranial tumor that causes significant morbidity, including hearing loss, tinnitus, dizziness, and possibly even death from brainstem compression. However, FDA-approved pharmacologic treatments for VS do not exist. Sulforaphane (SFN) is a naturally occurring isothiocyanate found in cruciferous vegetables, such as broccoli, with potent chemoprotective effects in several cell types. Our objective was to determine whether SFN is effective against VS in vitro and in vivo. Human primary VS cells, HEI-193 schwannoma cells, and SC4 Nf2(−/−) Schwann cells were used to investigate the inhibitory effects of SFN in vitro. Cell proliferation was assessed by bromodeoxyuridine (BrdU) incorporation, and cell viability and metabolic activity was calculated by MTT assay. Apoptosis was measured by flow cytometry, terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) staining, and Western blot for cleaved caspases. A mouse model with a murine schwannoma allograft was also used to examine the antitumor activity of SFN. SFN exhibited significant antiproliferative activity in schwannoma cells in vitro, via the inhibition of HDAC activity and the activation of ERK. SFN treatment induced apoptosis and cell cycle arrest at the G2/M phase. SFN also significantly inhibited schwannoma growth in vivo. Our preclinical studies motivate a future prospective clinical study of SFN for the treatment of VS.
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spelling pubmed-50902442016-11-08 Sulforaphane, a natural component of broccoli, inhibits vestibular schwannoma growth in vitro and in vivo Kim, Bo Gyung Fujita, Takeshi Stankovic, Konstantina M. Welling, D. Bradley Moon, In Seok Choi, Jae Young Yun, Jieun Kang, Jong Soon Lee, Jong Dae Sci Rep Article Vestibular schwannoma (VS) is an intracranial tumor that causes significant morbidity, including hearing loss, tinnitus, dizziness, and possibly even death from brainstem compression. However, FDA-approved pharmacologic treatments for VS do not exist. Sulforaphane (SFN) is a naturally occurring isothiocyanate found in cruciferous vegetables, such as broccoli, with potent chemoprotective effects in several cell types. Our objective was to determine whether SFN is effective against VS in vitro and in vivo. Human primary VS cells, HEI-193 schwannoma cells, and SC4 Nf2(−/−) Schwann cells were used to investigate the inhibitory effects of SFN in vitro. Cell proliferation was assessed by bromodeoxyuridine (BrdU) incorporation, and cell viability and metabolic activity was calculated by MTT assay. Apoptosis was measured by flow cytometry, terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) staining, and Western blot for cleaved caspases. A mouse model with a murine schwannoma allograft was also used to examine the antitumor activity of SFN. SFN exhibited significant antiproliferative activity in schwannoma cells in vitro, via the inhibition of HDAC activity and the activation of ERK. SFN treatment induced apoptosis and cell cycle arrest at the G2/M phase. SFN also significantly inhibited schwannoma growth in vivo. Our preclinical studies motivate a future prospective clinical study of SFN for the treatment of VS. Nature Publishing Group 2016-11-02 /pmc/articles/PMC5090244/ /pubmed/27805058 http://dx.doi.org/10.1038/srep36215 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Kim, Bo Gyung
Fujita, Takeshi
Stankovic, Konstantina M.
Welling, D. Bradley
Moon, In Seok
Choi, Jae Young
Yun, Jieun
Kang, Jong Soon
Lee, Jong Dae
Sulforaphane, a natural component of broccoli, inhibits vestibular schwannoma growth in vitro and in vivo
title Sulforaphane, a natural component of broccoli, inhibits vestibular schwannoma growth in vitro and in vivo
title_full Sulforaphane, a natural component of broccoli, inhibits vestibular schwannoma growth in vitro and in vivo
title_fullStr Sulforaphane, a natural component of broccoli, inhibits vestibular schwannoma growth in vitro and in vivo
title_full_unstemmed Sulforaphane, a natural component of broccoli, inhibits vestibular schwannoma growth in vitro and in vivo
title_short Sulforaphane, a natural component of broccoli, inhibits vestibular schwannoma growth in vitro and in vivo
title_sort sulforaphane, a natural component of broccoli, inhibits vestibular schwannoma growth in vitro and in vivo
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5090244/
https://www.ncbi.nlm.nih.gov/pubmed/27805058
http://dx.doi.org/10.1038/srep36215
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