Identification of biological pathways and processes regulated by NEK5 in breast epithelial cells via an integrated proteomic approach.

Autor: de Castro Ferezin C; Cancer Program, Biomedicine Discovery Institute, Monash University, Melbourne, VIC, 3800, Australia.; Department of Biochemistry and Molecular Biology, Monash University, Melbourne, VIC, 3800, Australia.; Faculty of Pharmaceutical Sciences, State University of Campinas, São Paulo, Brazil., Lim Kam Sian TCC; Cancer Program, Biomedicine Discovery Institute, Monash University, Melbourne, VIC, 3800, Australia.; Department of Biochemistry and Molecular Biology, Monash University, Melbourne, VIC, 3800, Australia., Wu Y; Cancer Program, Biomedicine Discovery Institute, Monash University, Melbourne, VIC, 3800, Australia.; Department of Biochemistry and Molecular Biology, Monash University, Melbourne, VIC, 3800, Australia., Ma X; Cancer Program, Biomedicine Discovery Institute, Monash University, Melbourne, VIC, 3800, Australia.; Department of Biochemistry and Molecular Biology, Monash University, Melbourne, VIC, 3800, Australia., Chüeh AC; Cancer Program, Biomedicine Discovery Institute, Monash University, Melbourne, VIC, 3800, Australia.; Department of Biochemistry and Molecular Biology, Monash University, Melbourne, VIC, 3800, Australia., Huang C; Department of Biochemistry and Molecular Biology, Monash University, Melbourne, VIC, 3800, Australia.; Monash Proteomics and Metabolomics Facility, Monash University, Melbourne, VIC, 3800, Australia., Schittenhelm RB; Department of Biochemistry and Molecular Biology, Monash University, Melbourne, VIC, 3800, Australia.; Monash Proteomics and Metabolomics Facility, Monash University, Melbourne, VIC, 3800, Australia., Kobarg J; Faculty of Pharmaceutical Sciences, State University of Campinas, São Paulo, Brazil., Daly RJ; Cancer Program, Biomedicine Discovery Institute, Monash University, Melbourne, VIC, 3800, Australia. roger.daly@monash.edu.; Department of Biochemistry and Molecular Biology, Monash University, Melbourne, VIC, 3800, Australia. roger.daly@monash.edu.
Jazyk: angličtina
Zdroj: Cell communication and signaling : CCS [Cell Commun Signal] 2022 Dec 22; Vol. 20 (1), pp. 197. Date of Electronic Publication: 2022 Dec 22.
DOI: 10.1186/s12964-022-01006-y
Abstrakt: Specific members of the Nima-Related Kinase (NEK) family have been linked to cancer development and progression, and a role for NEK5, one of the least studied members, in breast cancer has recently been proposed. However, while NEK5 is known to regulate centrosome separation and mitotic spindle assembly, NEK5 signalling mechanisms and function in this malignancy require further characterization. To this end, we established a model system featuring overexpression of NEK5 in the immortalized breast epithelial cell line MCF-10A. MCF-10A cells overexpressing NEK5 exhibited an increase in clonogenicity under monolayer conditions and enhanced acinar size and abnormal morphology in 3D Matrigel culture. Interestingly, they also exhibited a marked reduction in Src activation and downstream signalling. To interrogate NEK5 signalling and function in an unbiased manner, we applied a variety of MS-based proteomic approaches. Determination of the NEK5 interactome by Bio-ID identified a variety of protein classes including the kinesins KIF2C and KIF22, the mitochondrial proteins TFAM, TFB2M and MFN2, RhoH effectors and the negative regulator of Src, CSK. Characterization of proteins and phosphosites modulated upon NEK5 overexpression by global MS-based (phospho)proteomic profiling revealed impact on the cell cycle, DNA synthesis and repair, Rho GTPase signalling, the microtubule cytoskeleton and hemidesmosome assembly. Overall, the study indicates that NEK5 impacts diverse pathways and processes in breast epithelial cells, and likely plays a multifaceted role in breast cancer development and progression. Video Abstract.
(© 2022. The Author(s).)
Databáze: MEDLINE
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