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Tamoxifen Protects from Vesicular Stomatitis Virus Infection

Background: Tamoxifen (TAM) is an estrogen-receptor antagonist, widely used in the adjuvant treatment of early stage estrogen-sensitive breast cancer. Several studies have revealed new biological targets of TAM that mediate the estrogen receptor independent activities of the drug. Recently, the anti...

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Autores principales: Cham, Lamin B., Friedrich, Sarah-Kim, Adomati, Tom, Bhat, Hilal, Schiller, Maximilian, Bergerhausen, Michael, Hamdan, Thamer, Li, Fanghui, Machlah, Yara Maria, Ali, Murtaza, Duhan, Vikas, Lang, Karl Sebastian, Friebus-Kardash, Justa, Lang, Judith
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6958322/
https://www.ncbi.nlm.nih.gov/pubmed/31547012
http://dx.doi.org/10.3390/ph12040142
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author Cham, Lamin B.
Friedrich, Sarah-Kim
Adomati, Tom
Bhat, Hilal
Schiller, Maximilian
Bergerhausen, Michael
Hamdan, Thamer
Li, Fanghui
Machlah, Yara Maria
Ali, Murtaza
Duhan, Vikas
Lang, Karl Sebastian
Friebus-Kardash, Justa
Lang, Judith
author_facet Cham, Lamin B.
Friedrich, Sarah-Kim
Adomati, Tom
Bhat, Hilal
Schiller, Maximilian
Bergerhausen, Michael
Hamdan, Thamer
Li, Fanghui
Machlah, Yara Maria
Ali, Murtaza
Duhan, Vikas
Lang, Karl Sebastian
Friebus-Kardash, Justa
Lang, Judith
author_sort Cham, Lamin B.
collection PubMed
description Background: Tamoxifen (TAM) is an estrogen-receptor antagonist, widely used in the adjuvant treatment of early stage estrogen-sensitive breast cancer. Several studies have revealed new biological targets of TAM that mediate the estrogen receptor independent activities of the drug. Recently, the antiviral activity of TAM on replication of human immunodeficiency virus (HIV), hepatitis C virus (HCV) and Herpes simplex virus (HSV-1) in vitro was described. In the current study, we aimed to investigate the effect of TAM on infection with vesicular stomatitis virus (VSV). Methods: Vero cells were treated with different concentrations of TAM for 24 h and then infected with VSV. Additionally, C57BL/6 mice were pretreated with 4 mg TAM, one day and three days before infection with VSV. Results: Treatment of Vero cells with TAM suppressed the viral replication of VSV in vitro and in vivo. The inhibitory effect of TAM on VSV replication correlated with an enhanced interferon-I response and stimulation of macrophages. Conclusions: TAM was identified as being capable to protect from VSV infection in vitro and in vivo. Consequently, this antiviral function (as an advantageous side-effect of TAM) might give rise to new clinical applications, such as treatment of resistant virus infections, or serve as an add-on to standard antiviral therapy.
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spelling pubmed-69583222020-01-23 Tamoxifen Protects from Vesicular Stomatitis Virus Infection Cham, Lamin B. Friedrich, Sarah-Kim Adomati, Tom Bhat, Hilal Schiller, Maximilian Bergerhausen, Michael Hamdan, Thamer Li, Fanghui Machlah, Yara Maria Ali, Murtaza Duhan, Vikas Lang, Karl Sebastian Friebus-Kardash, Justa Lang, Judith Pharmaceuticals (Basel) Article Background: Tamoxifen (TAM) is an estrogen-receptor antagonist, widely used in the adjuvant treatment of early stage estrogen-sensitive breast cancer. Several studies have revealed new biological targets of TAM that mediate the estrogen receptor independent activities of the drug. Recently, the antiviral activity of TAM on replication of human immunodeficiency virus (HIV), hepatitis C virus (HCV) and Herpes simplex virus (HSV-1) in vitro was described. In the current study, we aimed to investigate the effect of TAM on infection with vesicular stomatitis virus (VSV). Methods: Vero cells were treated with different concentrations of TAM for 24 h and then infected with VSV. Additionally, C57BL/6 mice were pretreated with 4 mg TAM, one day and three days before infection with VSV. Results: Treatment of Vero cells with TAM suppressed the viral replication of VSV in vitro and in vivo. The inhibitory effect of TAM on VSV replication correlated with an enhanced interferon-I response and stimulation of macrophages. Conclusions: TAM was identified as being capable to protect from VSV infection in vitro and in vivo. Consequently, this antiviral function (as an advantageous side-effect of TAM) might give rise to new clinical applications, such as treatment of resistant virus infections, or serve as an add-on to standard antiviral therapy. MDPI 2019-09-20 /pmc/articles/PMC6958322/ /pubmed/31547012 http://dx.doi.org/10.3390/ph12040142 Text en © 2019 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
Cham, Lamin B.
Friedrich, Sarah-Kim
Adomati, Tom
Bhat, Hilal
Schiller, Maximilian
Bergerhausen, Michael
Hamdan, Thamer
Li, Fanghui
Machlah, Yara Maria
Ali, Murtaza
Duhan, Vikas
Lang, Karl Sebastian
Friebus-Kardash, Justa
Lang, Judith
Tamoxifen Protects from Vesicular Stomatitis Virus Infection
title Tamoxifen Protects from Vesicular Stomatitis Virus Infection
title_full Tamoxifen Protects from Vesicular Stomatitis Virus Infection
title_fullStr Tamoxifen Protects from Vesicular Stomatitis Virus Infection
title_full_unstemmed Tamoxifen Protects from Vesicular Stomatitis Virus Infection
title_short Tamoxifen Protects from Vesicular Stomatitis Virus Infection
title_sort tamoxifen protects from vesicular stomatitis virus infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6958322/
https://www.ncbi.nlm.nih.gov/pubmed/31547012
http://dx.doi.org/10.3390/ph12040142
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