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Endogenous c-Jun N-terminal kinase (JNK) activity marks the boundary between normal and malignant granulosa cells
Granulosa cell tumor of the ovary (GCT) is a very rare tumor, accounting for only 2% of all ovarian tumors. It originates from sex cords in the ovary and can be divided into adult (95%) and juvenile (5%) types based on histologic findings. To date, no clear etiologic process has been identified othe...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5856777/ https://www.ncbi.nlm.nih.gov/pubmed/29549247 http://dx.doi.org/10.1038/s41419-018-0459-3 |
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author | Bildik, Gamze Akin, Nazli Senbabaoglu, Filiz Esmalian, Yashar Sahin, Gizem Nur Urman, Defne Karahuseyinoglu, Sercin Ince, Umit Palaoglu, Erhan Taskiran, Cagatay Arvas, Macit Guzel, Yilmaz Yakin, Kayhan Oktem, Ozgur |
author_facet | Bildik, Gamze Akin, Nazli Senbabaoglu, Filiz Esmalian, Yashar Sahin, Gizem Nur Urman, Defne Karahuseyinoglu, Sercin Ince, Umit Palaoglu, Erhan Taskiran, Cagatay Arvas, Macit Guzel, Yilmaz Yakin, Kayhan Oktem, Ozgur |
author_sort | Bildik, Gamze |
collection | PubMed |
description | Granulosa cell tumor of the ovary (GCT) is a very rare tumor, accounting for only 2% of all ovarian tumors. It originates from sex cords in the ovary and can be divided into adult (95%) and juvenile (5%) types based on histologic findings. To date, no clear etiologic process has been identified other than a missense point mutation in the FOXL2 gene. Our previous works showed that c-Jun N-terminal kinase (JNK) pathway plays critical role in cell cycle progression and mitosis of normal and immortalized granulosa cells and follicle growth in rodent ovaries. These findings led us to investigate the role of JNK pathway in the granulosa cell tumor of the ovary. We used two different GCT cell lines (COV434 and KGN) and fresh GCT samples of adult and juvenile types obtained from the patients during surgery. We have discovered that endogenous kinase activity of JNK is markedly enhanced in the GCT samples and cell lines, whereas it was almost undetectable in mitotic non-malignant human granulosa cells. The inhibition of JNK pathway in GCT cell lines with two different pharmacologic inhibitors (SP600125 and AS601245) or siRNA resulted in a dose-dependent reduction in in vitro cell growth, increased apoptosis and diminished estradiol and AMH productions. JNK inhibition was also associated with a decrease in the number of cells positive for mitosis marker phospho-histone H3(Ser 10) in the asynchronous cells; and diminished EdU uptake during S phase and cell cycle arrest at G2/M-phase transition in the synchronized cells. Ex vivo treatment of patient-derived GCT samples with JNK inhibitors for 24 h significantly decreased their in vitro growth and estradiol and AMH productions. Furthermore, in human GCT xenograft model, in vivo tumor growth was significantly reduced and plasma AMH levels were significantly decreased in SCID mice after administration of JNK inhibitors and siRNA. These findings suggest that targeting JNK pathway may provide therapeutic benefit in the treatment of granulosa cell tumors for which currently no curative therapy exists beyond surgery. |
format | Online Article Text |
id | pubmed-5856777 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58567772018-06-04 Endogenous c-Jun N-terminal kinase (JNK) activity marks the boundary between normal and malignant granulosa cells Bildik, Gamze Akin, Nazli Senbabaoglu, Filiz Esmalian, Yashar Sahin, Gizem Nur Urman, Defne Karahuseyinoglu, Sercin Ince, Umit Palaoglu, Erhan Taskiran, Cagatay Arvas, Macit Guzel, Yilmaz Yakin, Kayhan Oktem, Ozgur Cell Death Dis Article Granulosa cell tumor of the ovary (GCT) is a very rare tumor, accounting for only 2% of all ovarian tumors. It originates from sex cords in the ovary and can be divided into adult (95%) and juvenile (5%) types based on histologic findings. To date, no clear etiologic process has been identified other than a missense point mutation in the FOXL2 gene. Our previous works showed that c-Jun N-terminal kinase (JNK) pathway plays critical role in cell cycle progression and mitosis of normal and immortalized granulosa cells and follicle growth in rodent ovaries. These findings led us to investigate the role of JNK pathway in the granulosa cell tumor of the ovary. We used two different GCT cell lines (COV434 and KGN) and fresh GCT samples of adult and juvenile types obtained from the patients during surgery. We have discovered that endogenous kinase activity of JNK is markedly enhanced in the GCT samples and cell lines, whereas it was almost undetectable in mitotic non-malignant human granulosa cells. The inhibition of JNK pathway in GCT cell lines with two different pharmacologic inhibitors (SP600125 and AS601245) or siRNA resulted in a dose-dependent reduction in in vitro cell growth, increased apoptosis and diminished estradiol and AMH productions. JNK inhibition was also associated with a decrease in the number of cells positive for mitosis marker phospho-histone H3(Ser 10) in the asynchronous cells; and diminished EdU uptake during S phase and cell cycle arrest at G2/M-phase transition in the synchronized cells. Ex vivo treatment of patient-derived GCT samples with JNK inhibitors for 24 h significantly decreased their in vitro growth and estradiol and AMH productions. Furthermore, in human GCT xenograft model, in vivo tumor growth was significantly reduced and plasma AMH levels were significantly decreased in SCID mice after administration of JNK inhibitors and siRNA. These findings suggest that targeting JNK pathway may provide therapeutic benefit in the treatment of granulosa cell tumors for which currently no curative therapy exists beyond surgery. Nature Publishing Group UK 2018-03-16 /pmc/articles/PMC5856777/ /pubmed/29549247 http://dx.doi.org/10.1038/s41419-018-0459-3 Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Bildik, Gamze Akin, Nazli Senbabaoglu, Filiz Esmalian, Yashar Sahin, Gizem Nur Urman, Defne Karahuseyinoglu, Sercin Ince, Umit Palaoglu, Erhan Taskiran, Cagatay Arvas, Macit Guzel, Yilmaz Yakin, Kayhan Oktem, Ozgur Endogenous c-Jun N-terminal kinase (JNK) activity marks the boundary between normal and malignant granulosa cells |
title | Endogenous c-Jun N-terminal kinase (JNK) activity marks the boundary between normal and malignant granulosa cells |
title_full | Endogenous c-Jun N-terminal kinase (JNK) activity marks the boundary between normal and malignant granulosa cells |
title_fullStr | Endogenous c-Jun N-terminal kinase (JNK) activity marks the boundary between normal and malignant granulosa cells |
title_full_unstemmed | Endogenous c-Jun N-terminal kinase (JNK) activity marks the boundary between normal and malignant granulosa cells |
title_short | Endogenous c-Jun N-terminal kinase (JNK) activity marks the boundary between normal and malignant granulosa cells |
title_sort | endogenous c-jun n-terminal kinase (jnk) activity marks the boundary between normal and malignant granulosa cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5856777/ https://www.ncbi.nlm.nih.gov/pubmed/29549247 http://dx.doi.org/10.1038/s41419-018-0459-3 |
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