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Sirtuin 1 and Sirtuin 3 in Granulosa Cell Tumors
Sirtuins (SIRTs) are NAD(+)-dependent deacetylases that regulate proliferation and cell death. In the human ovary, granulosa cells express sirtuin 1 (SIRT1), which has also been detected in human tumors derived from granulosa cells, i.e., granulosa cell tumors (GCTs), and in KGN cells. KGN cells are...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7923107/ https://www.ncbi.nlm.nih.gov/pubmed/33669567 http://dx.doi.org/10.3390/ijms22042047 |
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author | Schmid, Nina Dietrich, Kim-Gwendolyn Forne, Ignasi Burges, Alexander Szymanska, Magdalena Meidan, Rina Mayr, Doris Mayerhofer, Artur |
author_facet | Schmid, Nina Dietrich, Kim-Gwendolyn Forne, Ignasi Burges, Alexander Szymanska, Magdalena Meidan, Rina Mayr, Doris Mayerhofer, Artur |
author_sort | Schmid, Nina |
collection | PubMed |
description | Sirtuins (SIRTs) are NAD(+)-dependent deacetylases that regulate proliferation and cell death. In the human ovary, granulosa cells express sirtuin 1 (SIRT1), which has also been detected in human tumors derived from granulosa cells, i.e., granulosa cell tumors (GCTs), and in KGN cells. KGN cells are an established cellular model for the majority of GCTs and were used to explore the role of SIRT1. The SIRT1 activator SRT2104 increased cell proliferation. By contrast, the inhibitor EX527 reduced cell numbers, without inducing apoptosis. These results were supported by the outcome of siRNA-mediated silencing studies. A tissue microarray containing 92 GCTs revealed nuclear and/or cytoplasmic SIRT1 staining in the majority of the samples, and also, SIRT2-7 were detected in most samples. The expression of SIRT1–7 was not correlated with the survival of the patients; however, SIRT3 and SIRT7 expression was significantly correlated with the proliferation marker Ki-67, implying roles in tumor cell proliferation. SIRT3 was identified by a proteomic analysis as the most abundant SIRT in KGN. The results of the siRNA-silencing experiments indicate involvement of SIRT3 in proliferation. Thus, several SIRTs are expressed by GCTs, and SIRT1 and SIRT3 are involved in the growth regulation of KGN. If transferable to GCTs, these SIRTs may represent novel drug targets. |
format | Online Article Text |
id | pubmed-7923107 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-79231072021-03-03 Sirtuin 1 and Sirtuin 3 in Granulosa Cell Tumors Schmid, Nina Dietrich, Kim-Gwendolyn Forne, Ignasi Burges, Alexander Szymanska, Magdalena Meidan, Rina Mayr, Doris Mayerhofer, Artur Int J Mol Sci Article Sirtuins (SIRTs) are NAD(+)-dependent deacetylases that regulate proliferation and cell death. In the human ovary, granulosa cells express sirtuin 1 (SIRT1), which has also been detected in human tumors derived from granulosa cells, i.e., granulosa cell tumors (GCTs), and in KGN cells. KGN cells are an established cellular model for the majority of GCTs and were used to explore the role of SIRT1. The SIRT1 activator SRT2104 increased cell proliferation. By contrast, the inhibitor EX527 reduced cell numbers, without inducing apoptosis. These results were supported by the outcome of siRNA-mediated silencing studies. A tissue microarray containing 92 GCTs revealed nuclear and/or cytoplasmic SIRT1 staining in the majority of the samples, and also, SIRT2-7 were detected in most samples. The expression of SIRT1–7 was not correlated with the survival of the patients; however, SIRT3 and SIRT7 expression was significantly correlated with the proliferation marker Ki-67, implying roles in tumor cell proliferation. SIRT3 was identified by a proteomic analysis as the most abundant SIRT in KGN. The results of the siRNA-silencing experiments indicate involvement of SIRT3 in proliferation. Thus, several SIRTs are expressed by GCTs, and SIRT1 and SIRT3 are involved in the growth regulation of KGN. If transferable to GCTs, these SIRTs may represent novel drug targets. MDPI 2021-02-19 /pmc/articles/PMC7923107/ /pubmed/33669567 http://dx.doi.org/10.3390/ijms22042047 Text en © 2021 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 Schmid, Nina Dietrich, Kim-Gwendolyn Forne, Ignasi Burges, Alexander Szymanska, Magdalena Meidan, Rina Mayr, Doris Mayerhofer, Artur Sirtuin 1 and Sirtuin 3 in Granulosa Cell Tumors |
title | Sirtuin 1 and Sirtuin 3 in Granulosa Cell Tumors |
title_full | Sirtuin 1 and Sirtuin 3 in Granulosa Cell Tumors |
title_fullStr | Sirtuin 1 and Sirtuin 3 in Granulosa Cell Tumors |
title_full_unstemmed | Sirtuin 1 and Sirtuin 3 in Granulosa Cell Tumors |
title_short | Sirtuin 1 and Sirtuin 3 in Granulosa Cell Tumors |
title_sort | sirtuin 1 and sirtuin 3 in granulosa cell tumors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7923107/ https://www.ncbi.nlm.nih.gov/pubmed/33669567 http://dx.doi.org/10.3390/ijms22042047 |
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