Matches in SemOpenAlex for { <https://semopenalex.org/work/W2018518082> ?p ?o ?g. }
- W2018518082 endingPage "8127" @default.
- W2018518082 startingPage "8114" @default.
- W2018518082 abstract "Rituximab (chimeric anti-CD20 monoclonal antibodies) is currently being used in the treatment of B non-Hodgkin's lymphoma (NHL). We have recently reported that rituximab triggers and modifies various intracellular signaling pathways in NHL B-cell lines, resulting in reverting the chemoresistant phenotype to a sensitive phenotype. This study investigated whether rituximab also modifies intracellular signaling pathways resulting in the sensitization of NHL cells to Fas-induced apoptosis. Treatment of the Fas-resistant NHL cell lines (2F7, Ramos and Raji) with rituximab sensitized the cells to CH-11 (FasL agonist mAb)-induced apoptosis and synergy was achieved. Fas expression was upregulated by rituximab as early as 6 h post-treatment as determined by flow cytometry, reverse transcriptase–polymerase chain reaction and Western blot. Rituximab inhibited both the expression and activity of the transcription repressor Yin-Yang 1 (YY1) that negatively regulates Fas transcription. Inhibition of YY1 resulted in the upregulation of Fas expression and sensitization of the tumor cells to CH-11-induced apoptosis. The downregulation of YY1 expression was the result of rituximab-induced inhibition of both the p38 mitogen-activated protein kinase (MAPK) signaling pathway and constitutive nuclear factor κ of B cells (NF-κB) activity. The involvement of NF-κB and YY1 in the regulation of Fas expression was corroborated by the use of Ramos cells with a dominant-active inhibitor of NF-κB (Ramos IκB-estrogen receptor (ER) mutant) and by silencing YY1 with YY1 siRNA, respectively. Further, the role of rituximab-mediated inhibition of the p38 MAPK/NF-κB/YY1 pathway in the regulation of Fas and sensitization to CH-11-induced apoptosis was validated by the use of specific chemical inhibitors of this pathway and which mimicked rituximab-mediated effects. These findings provide a novel mechanism of rituximab-mediated activity by sensitizing NHL cells to Fas-induced apoptosis." @default.
- W2018518082 created "2016-06-24" @default.
- W2018518082 creator A5009014777 @default.
- W2018518082 creator A5010565662 @default.
- W2018518082 creator A5055490703 @default.
- W2018518082 creator A5078486942 @default.
- W2018518082 creator A5082889084 @default.
- W2018518082 date "2005-08-15" @default.
- W2018518082 modified "2023-10-18" @default.
- W2018518082 title "Rituximab (chimeric anti-CD20) sensitizes B-NHL cell lines to Fas-induced apoptosis" @default.
- W2018518082 cites W1938103646 @default.
- W2018518082 cites W1979419663 @default.
- W2018518082 cites W1985460392 @default.
- W2018518082 cites W2007436659 @default.
- W2018518082 cites W2013888495 @default.
- W2018518082 cites W2015788325 @default.
- W2018518082 cites W2017009058 @default.
- W2018518082 cites W2018011543 @default.
- W2018518082 cites W2028802255 @default.
- W2018518082 cites W2038258256 @default.
- W2018518082 cites W2063330398 @default.
- W2018518082 cites W2063792914 @default.
- W2018518082 cites W2068033067 @default.
- W2018518082 cites W2069524809 @default.
- W2018518082 cites W2078324381 @default.
- W2018518082 cites W2079756029 @default.
- W2018518082 cites W2080501134 @default.
- W2018518082 cites W2086769750 @default.
- W2018518082 cites W2090895449 @default.
- W2018518082 cites W2094471681 @default.
- W2018518082 cites W2098641105 @default.
- W2018518082 cites W2133003864 @default.
- W2018518082 cites W2144699392 @default.
- W2018518082 cites W2318772898 @default.
- W2018518082 cites W2399771188 @default.
- W2018518082 cites W42013536 @default.
- W2018518082 cites W60759546 @default.
- W2018518082 doi "https://doi.org/10.1038/sj.onc.1208954" @default.
- W2018518082 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/16103877" @default.
- W2018518082 hasPublicationYear "2005" @default.
- W2018518082 type Work @default.
- W2018518082 sameAs 2018518082 @default.
- W2018518082 citedByCount "94" @default.
- W2018518082 countsByYear W20185180822012 @default.
- W2018518082 countsByYear W20185180822013 @default.
- W2018518082 countsByYear W20185180822014 @default.
- W2018518082 countsByYear W20185180822015 @default.
- W2018518082 countsByYear W20185180822016 @default.
- W2018518082 countsByYear W20185180822017 @default.
- W2018518082 countsByYear W20185180822018 @default.
- W2018518082 countsByYear W20185180822019 @default.
- W2018518082 countsByYear W20185180822020 @default.
- W2018518082 countsByYear W20185180822021 @default.
- W2018518082 countsByYear W20185180822022 @default.
- W2018518082 crossrefType "journal-article" @default.
- W2018518082 hasAuthorship W2018518082A5009014777 @default.
- W2018518082 hasAuthorship W2018518082A5010565662 @default.
- W2018518082 hasAuthorship W2018518082A5055490703 @default.
- W2018518082 hasAuthorship W2018518082A5078486942 @default.
- W2018518082 hasAuthorship W2018518082A5082889084 @default.
- W2018518082 hasBestOaLocation W20185180821 @default.
- W2018518082 hasConcept C104317684 @default.
- W2018518082 hasConcept C127561419 @default.
- W2018518082 hasConcept C153911025 @default.
- W2018518082 hasConcept C190283241 @default.
- W2018518082 hasConcept C31573885 @default.
- W2018518082 hasConcept C502942594 @default.
- W2018518082 hasConcept C55493867 @default.
- W2018518082 hasConcept C57074206 @default.
- W2018518082 hasConcept C62478195 @default.
- W2018518082 hasConcept C66008609 @default.
- W2018518082 hasConcept C86803240 @default.
- W2018518082 hasConcept C95444343 @default.
- W2018518082 hasConceptScore W2018518082C104317684 @default.
- W2018518082 hasConceptScore W2018518082C127561419 @default.
- W2018518082 hasConceptScore W2018518082C153911025 @default.
- W2018518082 hasConceptScore W2018518082C190283241 @default.
- W2018518082 hasConceptScore W2018518082C31573885 @default.
- W2018518082 hasConceptScore W2018518082C502942594 @default.
- W2018518082 hasConceptScore W2018518082C55493867 @default.
- W2018518082 hasConceptScore W2018518082C57074206 @default.
- W2018518082 hasConceptScore W2018518082C62478195 @default.
- W2018518082 hasConceptScore W2018518082C66008609 @default.
- W2018518082 hasConceptScore W2018518082C86803240 @default.
- W2018518082 hasConceptScore W2018518082C95444343 @default.
- W2018518082 hasIssue "55" @default.
- W2018518082 hasLocation W20185180821 @default.
- W2018518082 hasLocation W20185180822 @default.
- W2018518082 hasOpenAccess W2018518082 @default.
- W2018518082 hasPrimaryLocation W20185180821 @default.
- W2018518082 hasRelatedWork W1985440419 @default.
- W2018518082 hasRelatedWork W1990035351 @default.
- W2018518082 hasRelatedWork W1996885323 @default.
- W2018518082 hasRelatedWork W2012209630 @default.
- W2018518082 hasRelatedWork W2032075286 @default.
- W2018518082 hasRelatedWork W2374432531 @default.
- W2018518082 hasRelatedWork W2391342691 @default.
- W2018518082 hasRelatedWork W2764177986 @default.