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PDLIM7 and CDH18 regulate the turnover of MDM2 during CDK4/6 inhibitor therapy-induced senescence
CDK4/6 inhibitors are being used to treat a variety of human malignancies. In well-differentiated and dedifferentiated liposarcoma their clinical promise is associated with their ability to downregulate the MDM2 protein. The downregulation of MDM2 following treatment with CDK4/6 inhibitors also indu...
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/PMC6137027/ https://www.ncbi.nlm.nih.gov/pubmed/29789718 http://dx.doi.org/10.1038/s41388-018-0332-y |
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author | Klein, Mary E. Dickson, Mark A. Antonescu, Cristina Qin, Li-Xuan Dooley, Scott J. Barlas, Afsar Manova, Katia Schwartz, Gary K. Crago, Aimee M. Singer, Samuel Koff, Andrew Tap, William D. |
author_facet | Klein, Mary E. Dickson, Mark A. Antonescu, Cristina Qin, Li-Xuan Dooley, Scott J. Barlas, Afsar Manova, Katia Schwartz, Gary K. Crago, Aimee M. Singer, Samuel Koff, Andrew Tap, William D. |
author_sort | Klein, Mary E. |
collection | PubMed |
description | CDK4/6 inhibitors are being used to treat a variety of human malignancies. In well-differentiated and dedifferentiated liposarcoma their clinical promise is associated with their ability to downregulate the MDM2 protein. The downregulation of MDM2 following treatment with CDK4/6 inhibitors also induces many cultured tumor cell lines derived from different types of malignancies to progress from quiescence into senescence. Here we used cultured human cell lines and defined a role for PDLIM7 and CDH18, regulating MDM2 protein in CDK4/6 inhibitor-treated cells. Materials from our previous phase II trials with palbociclib were then used to demonstrate that expression of CDH18 protein was associated with response, measured as both progression-free survival and overall survival. This supports the hypothesis that the biologic transition from quiescence to senescence has clinical relevance for this class of drugs. |
format | Online Article Text |
id | pubmed-6137027 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61370272018-09-17 PDLIM7 and CDH18 regulate the turnover of MDM2 during CDK4/6 inhibitor therapy-induced senescence Klein, Mary E. Dickson, Mark A. Antonescu, Cristina Qin, Li-Xuan Dooley, Scott J. Barlas, Afsar Manova, Katia Schwartz, Gary K. Crago, Aimee M. Singer, Samuel Koff, Andrew Tap, William D. Oncogene Article CDK4/6 inhibitors are being used to treat a variety of human malignancies. In well-differentiated and dedifferentiated liposarcoma their clinical promise is associated with their ability to downregulate the MDM2 protein. The downregulation of MDM2 following treatment with CDK4/6 inhibitors also induces many cultured tumor cell lines derived from different types of malignancies to progress from quiescence into senescence. Here we used cultured human cell lines and defined a role for PDLIM7 and CDH18, regulating MDM2 protein in CDK4/6 inhibitor-treated cells. Materials from our previous phase II trials with palbociclib were then used to demonstrate that expression of CDH18 protein was associated with response, measured as both progression-free survival and overall survival. This supports the hypothesis that the biologic transition from quiescence to senescence has clinical relevance for this class of drugs. Nature Publishing Group UK 2018-05-23 2018 /pmc/articles/PMC6137027/ /pubmed/29789718 http://dx.doi.org/10.1038/s41388-018-0332-y 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 Klein, Mary E. Dickson, Mark A. Antonescu, Cristina Qin, Li-Xuan Dooley, Scott J. Barlas, Afsar Manova, Katia Schwartz, Gary K. Crago, Aimee M. Singer, Samuel Koff, Andrew Tap, William D. PDLIM7 and CDH18 regulate the turnover of MDM2 during CDK4/6 inhibitor therapy-induced senescence |
title | PDLIM7 and CDH18 regulate the turnover of MDM2 during CDK4/6 inhibitor therapy-induced senescence |
title_full | PDLIM7 and CDH18 regulate the turnover of MDM2 during CDK4/6 inhibitor therapy-induced senescence |
title_fullStr | PDLIM7 and CDH18 regulate the turnover of MDM2 during CDK4/6 inhibitor therapy-induced senescence |
title_full_unstemmed | PDLIM7 and CDH18 regulate the turnover of MDM2 during CDK4/6 inhibitor therapy-induced senescence |
title_short | PDLIM7 and CDH18 regulate the turnover of MDM2 during CDK4/6 inhibitor therapy-induced senescence |
title_sort | pdlim7 and cdh18 regulate the turnover of mdm2 during cdk4/6 inhibitor therapy-induced senescence |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6137027/ https://www.ncbi.nlm.nih.gov/pubmed/29789718 http://dx.doi.org/10.1038/s41388-018-0332-y |
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