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The membrane-associated form of cyclin D1 enhances cellular invasion
The essential G(1)-cyclin, CCND1, is a collaborative nuclear oncogene that is frequently overexpressed in cancer. D-type cyclins bind and activate CDK4 and CDK6 thereby contributing to G(1)–S cell-cycle progression. In addition to the nucleus, herein cyclin D1 was also located in the cytoplasmic mem...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7501870/ https://www.ncbi.nlm.nih.gov/pubmed/32948740 http://dx.doi.org/10.1038/s41389-020-00266-y |
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author | Chen, Ke Jiao, Xuanmao Ashton, Anthony Di Rocco, Agnese Pestell, Timothy G. Sun, Yunguang Zhao, Jun Casimiro, Mathew C. Li, Zhiping Lisanti, Michael P. McCue, Peter A. Shen, Duanwen Achilefu, Samuel Rui, Hallgeir Pestell, Richard G. |
author_facet | Chen, Ke Jiao, Xuanmao Ashton, Anthony Di Rocco, Agnese Pestell, Timothy G. Sun, Yunguang Zhao, Jun Casimiro, Mathew C. Li, Zhiping Lisanti, Michael P. McCue, Peter A. Shen, Duanwen Achilefu, Samuel Rui, Hallgeir Pestell, Richard G. |
author_sort | Chen, Ke |
collection | PubMed |
description | The essential G(1)-cyclin, CCND1, is a collaborative nuclear oncogene that is frequently overexpressed in cancer. D-type cyclins bind and activate CDK4 and CDK6 thereby contributing to G(1)–S cell-cycle progression. In addition to the nucleus, herein cyclin D1 was also located in the cytoplasmic membrane. In contrast with the nuclear-localized form of cyclin D1 (cyclin D1(NL)), the cytoplasmic membrane-localized form of cyclin D1 (cyclin D1(MEM)) induced transwell migration and the velocity of cellular migration. The cyclin D1(MEM) was sufficient to induce G(1)–S cell-cycle progression, cellular proliferation, and colony formation. The cyclin D1(MEM) was sufficient to induce phosphorylation of the serine threonine kinase Akt (Ser473) and augmented extranuclear localized 17β-estradiol dendrimer conjugate (EDC)-mediated phosphorylation of Akt (Ser473). These studies suggest distinct subcellular compartments of cell cycle proteins may convey distinct functions. |
format | Online Article Text |
id | pubmed-7501870 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75018702020-10-05 The membrane-associated form of cyclin D1 enhances cellular invasion Chen, Ke Jiao, Xuanmao Ashton, Anthony Di Rocco, Agnese Pestell, Timothy G. Sun, Yunguang Zhao, Jun Casimiro, Mathew C. Li, Zhiping Lisanti, Michael P. McCue, Peter A. Shen, Duanwen Achilefu, Samuel Rui, Hallgeir Pestell, Richard G. Oncogenesis Article The essential G(1)-cyclin, CCND1, is a collaborative nuclear oncogene that is frequently overexpressed in cancer. D-type cyclins bind and activate CDK4 and CDK6 thereby contributing to G(1)–S cell-cycle progression. In addition to the nucleus, herein cyclin D1 was also located in the cytoplasmic membrane. In contrast with the nuclear-localized form of cyclin D1 (cyclin D1(NL)), the cytoplasmic membrane-localized form of cyclin D1 (cyclin D1(MEM)) induced transwell migration and the velocity of cellular migration. The cyclin D1(MEM) was sufficient to induce G(1)–S cell-cycle progression, cellular proliferation, and colony formation. The cyclin D1(MEM) was sufficient to induce phosphorylation of the serine threonine kinase Akt (Ser473) and augmented extranuclear localized 17β-estradiol dendrimer conjugate (EDC)-mediated phosphorylation of Akt (Ser473). These studies suggest distinct subcellular compartments of cell cycle proteins may convey distinct functions. Nature Publishing Group UK 2020-09-18 /pmc/articles/PMC7501870/ /pubmed/32948740 http://dx.doi.org/10.1038/s41389-020-00266-y Text en © The Author(s) 2020 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 Chen, Ke Jiao, Xuanmao Ashton, Anthony Di Rocco, Agnese Pestell, Timothy G. Sun, Yunguang Zhao, Jun Casimiro, Mathew C. Li, Zhiping Lisanti, Michael P. McCue, Peter A. Shen, Duanwen Achilefu, Samuel Rui, Hallgeir Pestell, Richard G. The membrane-associated form of cyclin D1 enhances cellular invasion |
title | The membrane-associated form of cyclin D1 enhances cellular invasion |
title_full | The membrane-associated form of cyclin D1 enhances cellular invasion |
title_fullStr | The membrane-associated form of cyclin D1 enhances cellular invasion |
title_full_unstemmed | The membrane-associated form of cyclin D1 enhances cellular invasion |
title_short | The membrane-associated form of cyclin D1 enhances cellular invasion |
title_sort | membrane-associated form of cyclin d1 enhances cellular invasion |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7501870/ https://www.ncbi.nlm.nih.gov/pubmed/32948740 http://dx.doi.org/10.1038/s41389-020-00266-y |
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