Major clinical response in a patient with leukemia cutis treated with the bromodomain inhibitor PLX51107 and azacitidine
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AUTHORS
Kim, et al
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Programs
OPN-51107
https://doi.org/10.1016/j.leukres.2022.106884
Inhibition of Bromodomain and Extra Terminal (BET) Domain Activity Modulates the IL-23R/IL-17 Axis and Suppresses Acute Graft- Versus-Host Disease
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AUTHORS
Snyder, et al
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Programs
OPN-2853, OPN-51107
https://doi.org/10.3389/fonc.2021.760789
A novel combination regimen of BET and FLT3 inhibition for FLT3-ITD acute myeloid leukemia
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AUTHORS
Lee, et al
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Programs
OPN-51107
https://doi.org/10.3324/haematol.2020.247346
BET inhibitors synergize with venetoclax to induce apoptosis in MYC-driven lymphomas with high BCL-2 expression
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AUTHORS
Cummin, et al
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Programs
OPN-2853, OPN-51107
https://doi.org/10.1182/bloodadvances.2020002231
Targeting BRD/BET proteins inhibits adaptive kinome upregulation and enhances the effects of BRAF/MEK inhibitors in melanoma
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AUTHORS
Tiago, et al
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Programs
OPN-51107
https://doi.org/10.1038/s41416-019-0724-y
PLX3397 inhibits the accumulation of intra-tumoral macrophages and improves bromodomain and extra-terminal inhibitor efficacy in melanoma
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AUTHORS
Erkes, et al
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Programs
OPN-51107
https://doi.org/10.1111/pcmr.12845
Potentiated anti-tumor effects of BETi by MEKi in anaplastic thyroid cancer
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AUTHORS
Zhu, et al
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Programs
OPN-51107
https://doi.org/10.1530/ERC-19-0107
The next-generation BET inhibitor, PLX51107, delays melanoma growth in a CD8-mediated manner
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AUTHORS
Erkes, et al
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Programs
OPN-51107
https://doi.org/10.1111/pcmr.12788
Inhibition of NF-κB-Dependent Signaling Enhances Sensitivity and Overcomes Resistance to BET Inhibition in Uveal Melanoma
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AUTHORS
Ambrosini, et al
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Programs
OPN-51107
https://doi.org/10.1158/0008-5472.CAN-18-3177
Stromal fibroblast growth factor 2 reduces the efficacy of bromodomain inhibitors in uveal melanoma
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AUTHORS
Chua, et al
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Programs
OPN-51107
https://doi.org/10.15252/emmm.201809081