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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...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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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. |
format | Online Article Text |
id | pubmed-6958322 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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