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TTK promotes mesenchymal signaling via multiple mechanisms in triple negative breast cancer

Abnormal expression of TTK kinase has been associated with the initiation, progression, and therapeutic resistance of breast and other cancers, but its roles remain to be clarified. In this study, we examined the role of TTK in triple negative breast cancer (TNBC), and found that higher TTK expressi...

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Autores principales: King, Jamie L., Zhang, Baotong, Li, Yixiang, Li, Kathy P., Ni, Jianping J., Saavedra, Harold I., Dong, Jin-Tang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6133923/
https://www.ncbi.nlm.nih.gov/pubmed/30206215
http://dx.doi.org/10.1038/s41389-018-0077-z
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author King, Jamie L.
Zhang, Baotong
Li, Yixiang
Li, Kathy P.
Ni, Jianping J.
Saavedra, Harold I.
Dong, Jin-Tang
author_facet King, Jamie L.
Zhang, Baotong
Li, Yixiang
Li, Kathy P.
Ni, Jianping J.
Saavedra, Harold I.
Dong, Jin-Tang
author_sort King, Jamie L.
collection PubMed
description Abnormal expression of TTK kinase has been associated with the initiation, progression, and therapeutic resistance of breast and other cancers, but its roles remain to be clarified. In this study, we examined the role of TTK in triple negative breast cancer (TNBC), and found that higher TTK expression correlated with mesenchymal and proliferative phenotypes in TNBC cells. Pharmacologic inhibition and genomic silencing of TTK not only reversed the epithelial-to-mesenchymal transition (EMT) in TNBC cells, but also increased the expression of KLF5, an effector of TGF-β signaling and inhibitor of EMT. In addition, TTK inhibition decreased the expression of EMT-associated micro-RNA miR-21 but increased the expression of miR-200 family members and suppressed TGF-β signaling. To test if upregulation of KLF5 plays a role in TTK-induced EMT, TTK and KLF5 were silenced simultaneously, which reversed the decreased EMT caused by loss of TTK. Consistently, the decrease in miR-21 expression and increase in miR-200 expression caused by TTK silencing were rescued by loss of KLF5. Altogether, this study highlights a novel role and signaling pathway for TTK in regulating EMT of TN breast cancer cells through TGF-β and KLF5 signaling, highlighting targetable signaling pathways for TTK inhibitors in aggressive breast cancer.
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spelling pubmed-61339232018-09-13 TTK promotes mesenchymal signaling via multiple mechanisms in triple negative breast cancer King, Jamie L. Zhang, Baotong Li, Yixiang Li, Kathy P. Ni, Jianping J. Saavedra, Harold I. Dong, Jin-Tang Oncogenesis Article Abnormal expression of TTK kinase has been associated with the initiation, progression, and therapeutic resistance of breast and other cancers, but its roles remain to be clarified. In this study, we examined the role of TTK in triple negative breast cancer (TNBC), and found that higher TTK expression correlated with mesenchymal and proliferative phenotypes in TNBC cells. Pharmacologic inhibition and genomic silencing of TTK not only reversed the epithelial-to-mesenchymal transition (EMT) in TNBC cells, but also increased the expression of KLF5, an effector of TGF-β signaling and inhibitor of EMT. In addition, TTK inhibition decreased the expression of EMT-associated micro-RNA miR-21 but increased the expression of miR-200 family members and suppressed TGF-β signaling. To test if upregulation of KLF5 plays a role in TTK-induced EMT, TTK and KLF5 were silenced simultaneously, which reversed the decreased EMT caused by loss of TTK. Consistently, the decrease in miR-21 expression and increase in miR-200 expression caused by TTK silencing were rescued by loss of KLF5. Altogether, this study highlights a novel role and signaling pathway for TTK in regulating EMT of TN breast cancer cells through TGF-β and KLF5 signaling, highlighting targetable signaling pathways for TTK inhibitors in aggressive breast cancer. Nature Publishing Group UK 2018-09-12 /pmc/articles/PMC6133923/ /pubmed/30206215 http://dx.doi.org/10.1038/s41389-018-0077-z 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
King, Jamie L.
Zhang, Baotong
Li, Yixiang
Li, Kathy P.
Ni, Jianping J.
Saavedra, Harold I.
Dong, Jin-Tang
TTK promotes mesenchymal signaling via multiple mechanisms in triple negative breast cancer
title TTK promotes mesenchymal signaling via multiple mechanisms in triple negative breast cancer
title_full TTK promotes mesenchymal signaling via multiple mechanisms in triple negative breast cancer
title_fullStr TTK promotes mesenchymal signaling via multiple mechanisms in triple negative breast cancer
title_full_unstemmed TTK promotes mesenchymal signaling via multiple mechanisms in triple negative breast cancer
title_short TTK promotes mesenchymal signaling via multiple mechanisms in triple negative breast cancer
title_sort ttk promotes mesenchymal signaling via multiple mechanisms in triple negative breast cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6133923/
https://www.ncbi.nlm.nih.gov/pubmed/30206215
http://dx.doi.org/10.1038/s41389-018-0077-z
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