scholarly journals HSP110 sustains chronic NF-κB signaling in activated B-cell diffuse large B-cell lymphoma through MyD88 stabilization

Blood ◽  
2018 ◽  
Vol 132 (5) ◽  
pp. 510-520 ◽  
Author(s):  
Christophe Boudesco ◽  
Els Verhoeyen ◽  
Laurent Martin ◽  
Catherine Chassagne-Clement ◽  
Leila Salmi ◽  
...  

Key Points HSP110 sustains chronic NF-κB signaling in ABC-DLBCL through MyD88 stability. HSP110 is highly expressed in cells of patients with ABC-DLBCL and correlates with MyD88 expression.

Blood ◽  
2016 ◽  
Vol 127 (22) ◽  
pp. 2732-2741 ◽  
Author(s):  
Gero Knittel ◽  
Paul Liedgens ◽  
Darya Korovkina ◽  
Jens M. Seeger ◽  
Yussor Al-Baldawi ◽  
...  

Key Points B-cell–specific expression of Myd88p.L252P leads to the development of DLBCL in mice. The Myd88p.L252P mutation cooperates with BCL2 amplifications in ABC-DLBCL lymphomagenesis in vivo.


Blood ◽  
2016 ◽  
Vol 128 (2) ◽  
pp. 239-248 ◽  
Author(s):  
Julie Marie Matthews ◽  
Shruti Bhatt ◽  
Matthew P. Patricelli ◽  
Tyzoon K. Nomanbhoy ◽  
Xiaoyu Jiang ◽  
...  

Key Points GCK signaling is activated in DLBCL, and this signaling is important to DLBCL proliferation and survival. Therapeutic targeting of GCK is feasible and may advance efforts to cure DLBCL patients.


Blood ◽  
2013 ◽  
Vol 122 (19) ◽  
pp. 3251-3262 ◽  
Author(s):  
Stefan K. Barta ◽  
Xiaonan Xue ◽  
Dan Wang ◽  
Roni Tamari ◽  
Jeannette Y. Lee ◽  
...  

Key Points Rituximab use is associated with significant improvement in all outcomes for patients with HIV-associated CD20-positive lymphomas. Infusional EPOCH chemotherapy is associated with better overall survival in patients with AIDS-related diffuse large B-cell lymphoma (DLBCL).


Blood ◽  
2016 ◽  
Vol 127 (12) ◽  
pp. 1564-1574 ◽  
Author(s):  
Tibor Bedekovics ◽  
Sajjad Hussain ◽  
Andrew L. Feldman ◽  
Paul J. Galardy

Key Points The neuronal marker UCH-L1 is induced in, and specifically augments the oncogene-induced transformation of, GCB cells. High levels of UCHL1 identify patients with GC DLBCL with an increased risk for poor outcomes.


Blood ◽  
2014 ◽  
Vol 123 (13) ◽  
pp. 2062-2065 ◽  
Author(s):  
David D. W. Twa ◽  
Fong Chun Chan ◽  
Susana Ben-Neriah ◽  
Bruce W. Woolcock ◽  
Anja Mottok ◽  
...  

Key Points Programmed death ligands 1 and 2 are rearranged at a frequency of 20% in PMBCL.


Blood ◽  
2019 ◽  
Vol 134 (12) ◽  
pp. 946-950 ◽  
Author(s):  
Suraya Elfrink ◽  
Charlotte M. de Winde ◽  
Michiel van den Brand ◽  
Madeleine Berendsen ◽  
Margaretha G. M. Roemer ◽  
...  

Key Points Loss-of-function mutations in CD37 occur predominantly in diffuse large B-cell lymphoma at immune-privileged sites. CD37-mutated lymphoma B cells show impaired CD37 cell-surface localization, which may have implications for anti-CD37 therapies.


Blood ◽  
2013 ◽  
Vol 121 (18) ◽  
pp. 3666-3674 ◽  
Author(s):  
Diane L. Trinh ◽  
David W. Scott ◽  
Ryan D. Morin ◽  
Maria Mendez-Lago ◽  
Jianghong An ◽  
...  

Key Points Recurrent mutations in FOXO1 affect the DNA binding domain and the T24 phosphorylation site, which disrupt interactions with 14-3-3. Presence of FOXO1 mutations is associated with decreased OS, particularly in DLBCL patients of the low-risk R-IPI categories.


Blood ◽  
2018 ◽  
Vol 131 (2) ◽  
pp. 174-181 ◽  
Author(s):  
Thierry Lamy ◽  
Gandhi Damaj ◽  
Pierre Soubeyran ◽  
Emmanuel Gyan ◽  
Guillaume Cartron ◽  
...  

Key Points For early-stage DLBCL, R-CHOP alone is not inferior to R-CHOP followed by RT.


Blood ◽  
2014 ◽  
Vol 123 (23) ◽  
pp. 3553-3562 ◽  
Author(s):  
Li Tao ◽  
James M. Foran ◽  
Christina A. Clarke ◽  
Scarlett L. Gomez ◽  
Theresa H. M. Keegan

Key Points Patients living in low SES neighborhoods had worse survival after DLBCL. Disparity was most striking in younger (non-Medicare) patients and after the introduction of rituximab.


Blood ◽  
2017 ◽  
Vol 129 (14) ◽  
pp. 1947-1957 ◽  
Author(s):  
Davide Rossi ◽  
Fary Diop ◽  
Elisa Spaccarotella ◽  
Sara Monti ◽  
Manuela Zanni ◽  
...  

Key Points Plasma cfDNA genotyping is as accurate as genotyping of the diagnostic biopsy in detecting clonal somatic mutations in DLBCL. Plasma cfDNA genotyping is a real-time, noninvasive tool that can be used to track clonal evolution in DLBCL.


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