RT Journal Article
SR Electronic
T1 Pan- and Isoform-specific Inhibition of the Bromodomain and Extra-terminal Proteins and Evaluation of Synergistic Potential With Entospletinib in Canine Lymphoma
JF Anticancer Research
JO Anticancer Res
FD International Institute of Anticancer Research
SP 3781
OP 3792
DO 10.21873/anticanres.14367
VO 40
IS 7
A1 WEIBO KONG
A1 SINA SENDER
A1 SIMON VILLA PEREZ
A1 ANETT SEKORA
A1 BARBARA RUETGEN
A1 CHRISTIAN JUNGHANSS
A1 INGO NOLTE
A1 HUGO MURUA ESCOBAR
YR 2020
UL http://ar.iiarjournals.org/content/40/7/3781.abstract
AB Background/Aim: Canine B-cell lymphoma represents a useful in vivo model for human diffuse large B-cell lymphoma (DLBCL). Pan-Bromodomain and extra-terminal (BET) inhibition targeting BRD2/3/4 and selective inhibition of BRD4, as well as spleen tyrosine kinase (SYK) inhibition, are currently evaluated as haematologic cancer therapy. Herein, we characterized the differences in the biologic response of isoform-specific or pan-BET inhibition alone or in combination with SYK inhibition. Materials and Methods: I-BET151 (pan-inhibitor) and AZD5153 (BRD4 inhibitor) were combined with Entospletinib (SYK inhibitor) and comparatively analysed in the canine DLBCL cell line CLBL-1. Dose- and time-dependent cellular responses were analysed by cell number, metabolic activity, apoptosis/necrosis, and cell morphology. The synergistic potential was evaluated through the Bliss independence model. Results: I-BET151 and AZD5153 showed significant dose- and time-dependent inhibitory effects. Adding Entospletinib to I-BET151 or AZD5153 had no additional synergistic effects. Conclusion: Entospletinib did not enhance the inhibitory effects of the pan- or isoform-specific BET.