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ETS1 phosphorylation at threonine 38 is associated with the cell of origin of diffuse large B cell lymphoma and sustains the growth of tumour cells

Articolo
Data di Pubblicazione:
2023
Citazione:
ETS1 phosphorylation at threonine 38 is associated with the cell of origin of diffuse large B cell lymphoma and sustains the growth of tumour cells / Chung, E. Y. L.; Sartori, G.; Ponzoni, M.; Cascione, L.; Priebe, V.; Xu-Monette, Z. Y.; Fang, X.; Zhang, M.; Visco, C.; Tzankov, A.; Rinaldi, A.; Sgrignani, J.; Zucca, E.; Rossi, D.; Cavalli, A.; Inghirami, G.; Scott, D. W.; Young, K. H.; Bertoni, F.. - In: BRITISH JOURNAL OF HAEMATOLOGY. - ISSN 0007-1048. - 203:2(2023), pp. 244-254. [10.1111/bjh.19018]
Abstract:
The transcriptional factor ETS1 is upregulated in 25% of diffuse large B cell lymphoma (DLBCL). Here, we studied the role of ETS1 phosphorylation at threonine 38, a marker for ETS1 activation, in DLBCL cellular models and clinical specimens. p-ETS1 was detected in activated B cell-like DLBCL (ABC), not in germinal centre B-cell-like DLBCL (GCB) cell lines and, accordingly, it was more common in ABC than GCB DLBCL diagnostic biopsies. MEK inhibition decreased both baseline and IgM stimulation-induced p-ETS1 levels. Genetic inhibition of phosphorylation of ETS1 at threonine 38 affected the growth and the BCR-mediated transcriptome program in DLBCL cell lines. Our data demonstrate that ETS1 phosphorylation at threonine 38 is important for the growth of DLBCL cells and its pharmacological inhibition could benefit lymphoma patients.
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
11q24.3 gain; diffuse large B-cell lymphoma (DLBCL); ETS1 Thr38 phosphorylation; MEK/ERK axis
Elenco autori:
Chung, E. Y. L.; Sartori, G.; Ponzoni, M.; Cascione, L.; Priebe, V.; Xu-Monette, Z. Y.; Fang, X.; Zhang, M.; Visco, C.; Tzankov, A.; Rinaldi, A.; Sgrignani, J.; Zucca, E.; Rossi, D.; Cavalli, A.; Inghirami, G.; Scott, D. W.; Young, K. H.; Bertoni, F.
Autori di Ateneo:
PONZONI MAURILIO
Link alla scheda completa:
https://iris.unisr.it/handle/20.500.11768/198260
Pubblicato in:
BRITISH JOURNAL OF HAEMATOLOGY
Journal
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