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Bruton's tyrosine kinase (Btk) inhibitor ibrutinib suppresses stem-like traits in ovarian cancer
According to a Prognoscan database, upregulation of Bruton's tyrosine kinase (Btk) is associated with low overall survival in ovarian cancer patients. We found that spheroids-forming ovarian cancer cell, which highly expressed cancer stem-like cell (CSC) markers and Btk, were cisplatin resistan...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4537012/ https://www.ncbi.nlm.nih.gov/pubmed/26036311 |
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author | Zucha, Muhammad Ary Wu, Alexander T.H. Lee, Wei-Hwa Wang, Liang-Shun Lin, Wan-Wan Yuan, Chiou-Chung Yeh, Chi-Tai |
author_facet | Zucha, Muhammad Ary Wu, Alexander T.H. Lee, Wei-Hwa Wang, Liang-Shun Lin, Wan-Wan Yuan, Chiou-Chung Yeh, Chi-Tai |
author_sort | Zucha, Muhammad Ary |
collection | PubMed |
description | According to a Prognoscan database, upregulation of Bruton's tyrosine kinase (Btk) is associated with low overall survival in ovarian cancer patients. We found that spheroids-forming ovarian cancer cell, which highly expressed cancer stem-like cell (CSC) markers and Btk, were cisplatin resistant. We next treated CSCs and non-CSCs by a combination of ibrutinib and cisplatin. We found that chemoresistance was dependent on Btk and JAK2/STAT3, which maintained CSC by inducing Sox-2 and prosurvival genes. We suggest that addition of ibrutinib to cisplatin may improve treatment outcome in ovarian cancer. |
format | Online Article Text |
id | pubmed-4537012 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-45370122015-08-26 Bruton's tyrosine kinase (Btk) inhibitor ibrutinib suppresses stem-like traits in ovarian cancer Zucha, Muhammad Ary Wu, Alexander T.H. Lee, Wei-Hwa Wang, Liang-Shun Lin, Wan-Wan Yuan, Chiou-Chung Yeh, Chi-Tai Oncotarget Research Paper According to a Prognoscan database, upregulation of Bruton's tyrosine kinase (Btk) is associated with low overall survival in ovarian cancer patients. We found that spheroids-forming ovarian cancer cell, which highly expressed cancer stem-like cell (CSC) markers and Btk, were cisplatin resistant. We next treated CSCs and non-CSCs by a combination of ibrutinib and cisplatin. We found that chemoresistance was dependent on Btk and JAK2/STAT3, which maintained CSC by inducing Sox-2 and prosurvival genes. We suggest that addition of ibrutinib to cisplatin may improve treatment outcome in ovarian cancer. Impact Journals LLC 2015-03-26 /pmc/articles/PMC4537012/ /pubmed/26036311 Text en Copyright: © 2015 Zucha et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Zucha, Muhammad Ary Wu, Alexander T.H. Lee, Wei-Hwa Wang, Liang-Shun Lin, Wan-Wan Yuan, Chiou-Chung Yeh, Chi-Tai Bruton's tyrosine kinase (Btk) inhibitor ibrutinib suppresses stem-like traits in ovarian cancer |
title | Bruton's tyrosine kinase (Btk) inhibitor ibrutinib suppresses stem-like traits in ovarian cancer |
title_full | Bruton's tyrosine kinase (Btk) inhibitor ibrutinib suppresses stem-like traits in ovarian cancer |
title_fullStr | Bruton's tyrosine kinase (Btk) inhibitor ibrutinib suppresses stem-like traits in ovarian cancer |
title_full_unstemmed | Bruton's tyrosine kinase (Btk) inhibitor ibrutinib suppresses stem-like traits in ovarian cancer |
title_short | Bruton's tyrosine kinase (Btk) inhibitor ibrutinib suppresses stem-like traits in ovarian cancer |
title_sort | bruton's tyrosine kinase (btk) inhibitor ibrutinib suppresses stem-like traits in ovarian cancer |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4537012/ https://www.ncbi.nlm.nih.gov/pubmed/26036311 |
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