Evidence map›Paper›PMID 25733167›Full record

ArticleLeukemia2015

IL10 receptor is a novel therapeutic target in DLBCLs.

W Béguelin, S Sawh, N Chambwe, F C Chan, Y Jiang, J-W Choo, D W Scott, A Chalmers, H Geng, L Tsikitas and 4 more

Registry-linked trialAbstract read
PubMed Publisher
In one paragraph

Article in Leukemia, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06847529 (Systemic Inflammatory Markers As a Prognostic Index for B-cell Neoplasm , Single Center Experience .), which is not on this map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
5.3field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT06847529 not yet recruitingnot on this mapstarted 2025, after this paper: background citation

Systemic Inflammatory Markers As a Prognostic Index for B-cell Neoplasm , Single Center Experience .

TypeobservationalSponsorAssiut UniversityRan2025 to 2025Enrolled70ConditionsB-cell Neoplasm
3 · Its place in the literature

Who cites it

51 citing papers in PubMed, 71 citations in OpenAlex.

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  12. TRAF3 loss-of-function reveals the noncanonical NF-κB pathway as a therapeutic target in diffuse large B cell lymphoma.Proceedings of the National Academy of Sciences of the United States of America · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 4 institutions in 2 countries.

W BéguelinDepartment of Medicine, Division of Hematology and Oncology, Weill Cornell Medical College, New York, NY, USA.
S SawhDepartment of Medicine, Division of Hematology and Oncology, Weill Cornell Medical College, New York, NY, USA.
N Chambwe1] The HRH Prince Alwaleed Bin Talal Bin Abdulaziz Alsaud Institute for Computational Biomedicine, Weill Cornell Medical College, New York, NY, USA [2] Department of Physiology and Biophysics, Weill Cornell Medical College, New York, NY, USA [3] Tri-Instituitional Training Program in Computational Biology and Medicine, Weill Cornell Medical College, New York, NY, USA.
F C ChanCentre for Lymphoid Cancer, British Columbia Cancer Agency, Vancouver, BC, Canada.
Y JiangDepartment of Medicine, Division of Hematology and Oncology, Weill Cornell Medical College, New York, NY, USA.
J-W ChooDepartment of Medicine, Division of Hematology and Oncology, Weill Cornell Medical College, New York, NY, USA.
D W ScottCentre for Lymphoid Cancer, British Columbia Cancer Agency, Vancouver, BC, Canada.
A ChalmersDepartment of Medicine, Division of Hematology and Oncology, Weill Cornell Medical College, New York, NY, USA.
H GengDepartment of Laboratory Medicine, University of California San Francisco, San Francisco, CA, USA.
L TsikitasDepartment of Medicine, Division of Hematology and Oncology, Weill Cornell Medical College, New York, NY, USA.
W TamDepartment of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, NY, USA.
G BhagatDepartment of Pathology and Cell Biology, Columbia University Medical Center, New York, NY, USA.ORCID 000000016250048X
R D Gascoyne1] Centre for Lymphoid Cancer, British Columbia Cancer Agency, Vancouver, BC, Canada [2] Department of Pathology, University of British Columbia, Vancouver, BC, Canada.
R Shaknovich1] Department of Medicine, Division of Hematology and Oncology, Weill Cornell Medical College, New York, NY, USA [2] Department of Pathology and Cell Biology, Columbia University Medical Center, New York, NY, USA.
Cornell University · USBC Cancer Agency · CAColumbia University Irving Medical Center · USUniversity of California, San Francisco · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diffuse large B-cell lymphoma (DLBCL) is a biologically and clinically heterogeneous disease with marked genomic instability and variable response to conventional R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone) chemotherapy. More clinically aggressive cases of DLBCLs have high level of circulating interleukin 10 (IL10) cytokine and evidence of activated intracellular STAT3 (signal transducer and activator of transcription 3) signaling. We investigated the role of IL10 and its surface receptor in supporting the neoplastic phenotype of DLBCLs. We determined that IL10RA gene is amplified in 21% and IL10RB gene in 10% of primary DLBCLs. Gene expression of IL10, IL10RA and IL10RB was markedly elevated in DLBCLs. We hypothesized that DLBCLs depend for their proliferation and survival on IL10-STAT3 signaling and that blocking the IL10 receptor (IL10R) would induce cell death. We used anti-IL10R blocking antibody, which resulted in a dose-dependent cell death in all tested activated B-cell-like subtype of DLBCL cell lines and primary DLBCLs. Response of germinal center B-cell-like subtype of DLBCL cell lines to anti-IL10R antibody varied from sensitive to resistant. Cells underwent cell cycle arrest, followed by induction of apoptosis. Cell death depended on inhibition of STAT3 and, to a lesser extent, STAT1 signaling. Anti-IL10R treatment resulted in interruption of IL10-IL10R autostimulatory loop. We thus propose that IL10R is a novel therapeutic target in DLBCLs.

Indexed as

ApoptosisBiomarkers, TumorBlotting, WesternCell CycleCell ProliferationHigh-Throughput Nucleotide SequencingHumansImmunoenzyme TechniquesInterleukin-10Lymphoma, Large B-Cell, DiffuseNeoplasm StagingPrognosisReal-Time Polymerase Chain ReactionReceptors, Interleukin-10Reverse Transcriptase Polymerase Chain ReactionRNA, MessengerBiomarkers, TumorInterleukin-10Receptors, Interleukin-10RNA, Messenger

Identifiers

PMID25733167
OpenAlexW1965807814

What OpenQuestion holds

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Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.