Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
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
Descripción
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.