PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 25565020-0 2015 Ibrutinib inhibits BTK-driven NF-kappaB p65 activity to overcome bortezomib-resistance in multiple myeloma. Bortezomib 65-75 Bruton tyrosine kinase Homo sapiens 19-22 25565020-4 2015 We identified enhanced Bruton"s tyrosine kinase (BTK) activity in bortezomib-resistant MM cells and found that inhibition of BTK, either pharmacologically with ibrutinib (0.5 muM) or via lenti-viral miRNA-targeted BTK interference, re-sensitized previously bortezomib-resistant MM cells to further bortezomib therapy at a physiologically relevant concentration (5 nM). Bortezomib 66-76 Bruton tyrosine kinase Homo sapiens 23-47 25565020-4 2015 We identified enhanced Bruton"s tyrosine kinase (BTK) activity in bortezomib-resistant MM cells and found that inhibition of BTK, either pharmacologically with ibrutinib (0.5 muM) or via lenti-viral miRNA-targeted BTK interference, re-sensitized previously bortezomib-resistant MM cells to further bortezomib therapy at a physiologically relevant concentration (5 nM). Bortezomib 66-76 Bruton tyrosine kinase Homo sapiens 49-52 25565020-4 2015 We identified enhanced Bruton"s tyrosine kinase (BTK) activity in bortezomib-resistant MM cells and found that inhibition of BTK, either pharmacologically with ibrutinib (0.5 muM) or via lenti-viral miRNA-targeted BTK interference, re-sensitized previously bortezomib-resistant MM cells to further bortezomib therapy at a physiologically relevant concentration (5 nM). Bortezomib 257-267 Bruton tyrosine kinase Homo sapiens 23-47 25565020-4 2015 We identified enhanced Bruton"s tyrosine kinase (BTK) activity in bortezomib-resistant MM cells and found that inhibition of BTK, either pharmacologically with ibrutinib (0.5 muM) or via lenti-viral miRNA-targeted BTK interference, re-sensitized previously bortezomib-resistant MM cells to further bortezomib therapy at a physiologically relevant concentration (5 nM). Bortezomib 257-267 Bruton tyrosine kinase Homo sapiens 23-47 22975686-0 2013 BTK inhibitor ibrutinib is cytotoxic to myeloma and potently enhances bortezomib and lenalidomide activities through NF-kappaB. Bortezomib 70-80 Bruton tyrosine kinase Homo sapiens 0-3 34508613-0 2021 Bortezomib enhances the anti-cancer effect of the novel Bruton"s tyrosine kinase inhibitor (BGB-3111) in mantle cell lymphoma expressing BTK. Bortezomib 0-10 Bruton tyrosine kinase Homo sapiens 56-80 34508613-0 2021 Bortezomib enhances the anti-cancer effect of the novel Bruton"s tyrosine kinase inhibitor (BGB-3111) in mantle cell lymphoma expressing BTK. Bortezomib 0-10 Bruton tyrosine kinase Homo sapiens 137-140 34508613-2 2021 This study aimed to investigate the anti-cancer effects of BGB-3111 combined with bortezomib (BTZ) against the BTK-expressing MCL. Bortezomib 82-92 Bruton tyrosine kinase Homo sapiens 111-114 34508613-2 2021 This study aimed to investigate the anti-cancer effects of BGB-3111 combined with bortezomib (BTZ) against the BTK-expressing MCL. Bortezomib 94-97 Bruton tyrosine kinase Homo sapiens 111-114 24156429-6 2013 It is concluded that PCI-32765 and bortezomib can synergistically inhibit the proliferation and induce apoptosis of Raji and Ramos cells, the mechanism may be associated with inhibition of Btk and NFkappaB activity, down-regulation of anti-apoptotic proteins expression, such as Bcl-xl and c-IAP1, and increase of caspase-3 expression. Bortezomib 35-45 Bruton tyrosine kinase Homo sapiens 189-192 23360303-0 2013 The Bruton tyrosine kinase (BTK) inhibitor PCI-32765 synergistically increases proteasome inhibitor activity in diffuse large-B cell lymphoma (DLBCL) and mantle cell lymphoma (MCL) cells sensitive or resistant to bortezomib. Bortezomib 213-223 Bruton tyrosine kinase Homo sapiens 4-26 23360303-0 2013 The Bruton tyrosine kinase (BTK) inhibitor PCI-32765 synergistically increases proteasome inhibitor activity in diffuse large-B cell lymphoma (DLBCL) and mantle cell lymphoma (MCL) cells sensitive or resistant to bortezomib. Bortezomib 213-223 Bruton tyrosine kinase Homo sapiens 28-31