Author

Konstantinos Stamatiou

Brunel University of LondonORCID 0000-0002-5650-078XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Organism:human· 3 Assay:proteomics· 2 Research Focus:cancer & tumor microenvironment· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Assay:ChIP-seq· 1 Research Focus:chromatin & epigenetic regulation· 1

Frequent Co-Authors

Paola VagnarelliiD· 3 shared Amirhossein SakhtemaniD· 1 shared Antje GabrieliD· 1 shared Antonia Tsavou· 1 shared Arturo SalaiD· 1 shared Bernhard KüsteriD· 1 shared Christina LudwigiD· 1 shared Christos SpanosiD· 1 shared

Activity by Year

2025-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 19 mutual co-author links

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3 shared papersCell Biology

Paola VagnarelliORCID

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3 papers

Recent·Most cited

Cell BiologyDevelopmental CellPeer-reviewedMar 17, 2026

Multi-omic analyses reveal a differential contribution of chromatin-associated PP1 holoenzymes to mitotic exit and G1 re-establishment.

Konstantinos Stamatiou, Florentin Huguet, Marta Izabela Budzinska…·Paola Vagnarelli

The paper investigates the role of three chromatin-associated PP1 targeting subunits in mitotic exit and G1 re-establishment using multi-omic analyses.

2 citations

humanChIP-seq

Cell BiologyOpen BiologyPeer-reviewedMar 11, 2026

A CDCA2 - MYC positive feedback loop controls cancer cells survival

Konstantinos Stamatiou, Lorena Ligammari, Malki Bothota…·Paola Vagnarelli

The paper identifies a CDCA2-MYC positive feedback loop that promotes cancer cell survival in multiple cancer types.

DOI 10.1098/rsob.250075

humanexperimental assay

Cell BiologyScience SignalingPeer-reviewedJul 29, 2025

Illuminating oncogenic KRAS signaling by multi-dimensional chemical proteomics

Nicole Kabella, Florian P Bayer, Konstantinos Stamatiou…·Bernhard Küster

The paper uses chemical proteomics to analyze KRAS inhibitor effects on signaling networks in cancer cells, revealing cell-specific responses and phosphorylation changes.

8 citations

humanproteomics