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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 |
Sumario: | 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. |
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