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Methylsulfonylmethane sensitizes endometrial cancer cells to doxorubicin
BACKGROUND: Methylsulfonylmethane (MSM) is a commonly used diet supplement believed to decrease the inflammation in joints and fastens recovery in osteoarthritis, gastric mucosal injury, or obesity-related disorders. It was also suggested that MSM might play a beneficial role in cancer treatment. PU...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8012311/ https://www.ncbi.nlm.nih.gov/pubmed/32562081 http://dx.doi.org/10.1007/s10565-020-09542-4 |
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author | Kowalska, Karolina Habrowska-Górczyńska, Dominika Ewa Kurczewska, Dominika Domińska, Kamila Urbanek, Kinga Anna Piastowska-Ciesielska, Agnieszka Wanda |
author_facet | Kowalska, Karolina Habrowska-Górczyńska, Dominika Ewa Kurczewska, Dominika Domińska, Kamila Urbanek, Kinga Anna Piastowska-Ciesielska, Agnieszka Wanda |
author_sort | Kowalska, Karolina |
collection | PubMed |
description | BACKGROUND: Methylsulfonylmethane (MSM) is a commonly used diet supplement believed to decrease the inflammation in joints and fastens recovery in osteoarthritis, gastric mucosal injury, or obesity-related disorders. It was also suggested that MSM might play a beneficial role in cancer treatment. PURPOSE: So far, the MSM might have a potentially beneficial effect in endometrial cancer (EC) treatment. STUDY DESIGN: This study evaluated the effect and usefulness of MSM in combinatory therapy with known drug doxorubicin (DOX). METHODS: The effect of combinational treatment of MSM and DOX on the induction of apoptosis was evaluated in EC cell lines (ISHIKAWA, MFE-296, MFE-280). RESULTS: We observed that MSM itself induces apoptosis in EC cell lines, and pre-treatment with MSM for 24 h increases the sensitivity of EC cells to DOX-induced apoptosis and DNA damage and that effect might be regulated by p42/44 (Erk1/2) MAPK and Akt (protein kinase B). CONCLUSION: These results for the first time show that MSM might act as a sensitizer of EC cells to known drugs, for which EC cells quickly acquire resistance. [Figure: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10565-020-09542-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-8012311 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-80123112021-04-16 Methylsulfonylmethane sensitizes endometrial cancer cells to doxorubicin Kowalska, Karolina Habrowska-Górczyńska, Dominika Ewa Kurczewska, Dominika Domińska, Kamila Urbanek, Kinga Anna Piastowska-Ciesielska, Agnieszka Wanda Cell Biol Toxicol Original Article BACKGROUND: Methylsulfonylmethane (MSM) is a commonly used diet supplement believed to decrease the inflammation in joints and fastens recovery in osteoarthritis, gastric mucosal injury, or obesity-related disorders. It was also suggested that MSM might play a beneficial role in cancer treatment. PURPOSE: So far, the MSM might have a potentially beneficial effect in endometrial cancer (EC) treatment. STUDY DESIGN: This study evaluated the effect and usefulness of MSM in combinatory therapy with known drug doxorubicin (DOX). METHODS: The effect of combinational treatment of MSM and DOX on the induction of apoptosis was evaluated in EC cell lines (ISHIKAWA, MFE-296, MFE-280). RESULTS: We observed that MSM itself induces apoptosis in EC cell lines, and pre-treatment with MSM for 24 h increases the sensitivity of EC cells to DOX-induced apoptosis and DNA damage and that effect might be regulated by p42/44 (Erk1/2) MAPK and Akt (protein kinase B). CONCLUSION: These results for the first time show that MSM might act as a sensitizer of EC cells to known drugs, for which EC cells quickly acquire resistance. [Figure: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10565-020-09542-4) contains supplementary material, which is available to authorized users. Springer Netherlands 2020-06-20 2021 /pmc/articles/PMC8012311/ /pubmed/32562081 http://dx.doi.org/10.1007/s10565-020-09542-4 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Original Article Kowalska, Karolina Habrowska-Górczyńska, Dominika Ewa Kurczewska, Dominika Domińska, Kamila Urbanek, Kinga Anna Piastowska-Ciesielska, Agnieszka Wanda Methylsulfonylmethane sensitizes endometrial cancer cells to doxorubicin |
title | Methylsulfonylmethane sensitizes endometrial cancer cells to doxorubicin |
title_full | Methylsulfonylmethane sensitizes endometrial cancer cells to doxorubicin |
title_fullStr | Methylsulfonylmethane sensitizes endometrial cancer cells to doxorubicin |
title_full_unstemmed | Methylsulfonylmethane sensitizes endometrial cancer cells to doxorubicin |
title_short | Methylsulfonylmethane sensitizes endometrial cancer cells to doxorubicin |
title_sort | methylsulfonylmethane sensitizes endometrial cancer cells to doxorubicin |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8012311/ https://www.ncbi.nlm.nih.gov/pubmed/32562081 http://dx.doi.org/10.1007/s10565-020-09542-4 |
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