Author

B. Soysal

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Cancer Biology· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Assay:proteomics· 2 Assay:ATAC-seq· 1 Assay:bulk RNA-seq· 1 Research Focus:cancer & tumor microenvironment· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1

Frequent Co-Authors

E. Chavdoula· 2 shared P. N. Tsichlis· 2 shared V. Anastas· 2 shared A. La Ferlita· 1 shared A. Sircar· 1 shared E.-A. Fraile· 1 shared G. Carota· 1 shared G. Nigita· 1 shared

Activity by Year

2020-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 39 mutual co-author links

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2 shared papersCancer Biology

E. Chavdoula

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2 papers

Recent·Most cited

Transcriptional regulation of amino acid metabolism by KDM2B, in the context of ncPRC1.1 and in concert with MYC and ATF4

E. Chavdoula, V. Anastas, A. La Ferlita, J. Aldana, G. Carota, M. Spampinato, B. Soysal, I. Cosentini, S. Parashar, A. Sircar, G. Nigita, L. Sehgal, M. A. Freitas, P. N. Tsichlis

This study identifies KDM2B's role in regulating amino acid metabolism through interactions with ncPRC1.1, MYC, and ATF4, revealing a metabolic network linked to poor prognosis in TNBC.

bioRxiv · Jul 7, 2023Cancer Biology

KDM2B Silencing Elicits a Paracrine Mechanism Which Destabilizes SLUG, Promoting Differentiation of Basal-Like Breast Cancer Cells.

E.-A. Fraile, B. Soysal, V. Anastas, Z. T. Soysal, O. Serebrennikova, M. D. Paraskevopoulou, E. Chavdoula, P. N. Tsichlis

This paper shows that silencing KDM2B triggers a paracrine mechanism that inactivates GSK3, leading to SLUG degradation and differentiation of basal-like breast cancer cells.

bioRxiv · May 21, 2020 · PreprintCancer Biology