TIMP-1 regulation of cell cycle in human breast epithelial cells via stabilization of p27KIP1 protein
| Autor: | R. Fridman, Xu Wen Liu, M. E. Taube, Hyeong Reh Choi Kim |
|---|---|
| Rok vydání: | 2006 |
| Předmět: |
Proteasome Endopeptidase Complex
Cancer Research Leupeptins Cyclin D Cyclin A Cyclin B Retinoblastoma Protein Cell Line Cell Adhesion Genetics Humans Cyclin D1 Protease Inhibitors Anoikis Breast RNA Messenger Cycloheximide Phosphorylation Molecular Biology Protein Synthesis Inhibitors Tissue Inhibitor of Metalloproteinase-1 biology Cell growth Cell Cycle Intracellular Signaling Peptides and Proteins Retinoblastoma protein Epithelial Cells Cell cycle Cell biology Gene Expression Regulation biology.protein Cancer research Female Protein Processing Post-Translational Restriction point Cyclin-Dependent Kinase Inhibitor p27 |
| Zdroj: | Oncogene. 25:3041-3048 |
| ISSN: | 1476-5594 0950-9232 |
| DOI: | 10.1038/sj.onc.1209336 |
| Popis: | Increasing evidence suggests that tissue inhibitor of metalloproteinases-1 (TIMP-1) can directly regulate cell growth and apoptosis independent of its matrix metalloproteinases (MMPs)-inhibitory activity. While TIMP-1's antiapoptotic activity has been well demonstrated, conflicting data has been reported regarding TIMP-1's role in growth regulation. Here we show that TIMP-1 reduces the growth rate of human breast epithelial (MCF10A) cells by inducing cell cycle arrest at G(1). TIMP-1-mediated cell cycle arrest is associated with its downregulation of cyclin D(1) and upregulation of p27(KIP1), resulting in inhibition of cyclin-dependent kinase activity necessary for phosphorylation of the tumor suppressor retinoblastoma protein. We further show that TIMP-1 modulation of cyclin D(1) and p27(KIP1) is achieved through TIMP-1-mediated differential regulation of protein stability independent of growth factor signaling. We also show that TIMP-1-mediated differential regulation of cyclin D(1) and p27(KIP1) is independent of cell adhesion signaling. Whereas approximately 50% of MCF10A cells with reduced TIMP-1 expression underwent cell death following loss of cell adhesion (anoikis), TIMP-1 overexpressing cells remained viable with prominent cell cycle arrest without detectable cell death. Taken together, we propose that TIMP-1-mediated cell survival independent of cell adhesion is accompanied with cell cycle arrest in human breast epithelial cells, although cell cycle regulation may not be a prerequisite for TIMP-1 regulation of apoptosis in general. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|