Evidence map›Paper›PMID 30209121›Full record

ArticleBlood2018

B-cell receptor-mediated NFATc1 activation induces IL-10/STAT3/PD-L1 signaling in diffuse large B-cell lymphoma.

Li Li, Jun Zhang, Juan Chen, Zijun Y Xu-Monette, Yi Miao, Min Xiao, Ken H Young, Sa Wang, L Jeffrey Medeiros, Michael Wang and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
7.8field-weighted citation impact, top 2% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

57 citing papers in PubMed, 94 citations in OpenAlex.

  1. Review
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  18. Recent advances in CD5Annals of hematology · 2024
    Review
  19. Review
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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

12 authors at 1 institution in 2 countries.

Li LiDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX.
Jun ZhangDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX.
Juan ChenDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX.
Zijun Y Xu-MonetteDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX.
Yi MiaoDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX.
Min XiaoDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX.
Ken H YoungDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX.
Sa WangDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX.
L Jeffrey MedeirosDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX.
Michael WangDepartment of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX.
Richard J FordDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX.
Lan V PhamDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX.
The University of Texas MD Anderson Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

Knowledge of programmed death ligand 1 (PD-L1) expression and its regulation in B-cell lymphoma cells is limited. Investigating mechanisms that control PD-L1 expression in B-cell lymphoma cells might identify biomarkers that predict the efficacy of immunotherapy with anti-programmed death-1/PD-L1 antibodies. In addition, identification of mechanisms that regulate PD-L1 may identify molecules that can be targeted to improve the clinical efficacy of immune checkpoint inhibitors. In this study, we used proteomic approaches and patient-derived B-cell lymphoma cell lines to investigate mechanisms that regulate PD-L1 expression. We found that PD-L1 expression, particularly in nongerminal center B cell-derived diffuse large B-cell lymphoma (DLBCL), is controlled and regulated by several interactive signaling pathways, including the B-cell receptor (BCR) and JAK2/STAT3 signaling pathways. We found that that BCR-mediated NFATc1 activation upregulates IL-10 chemokine expression in PD-L1

Indexed as

B7-H1 AntigenGene Expression Regulation, LeukemicHumansInterleukin-10Lymphoma, Large B-Cell, DiffuseNFATC Transcription FactorsReceptors, Antigen, B-CellSignal TransductionSTAT3 Transcription FactorB7-H1 AntigenCD274 protein, humanIL10 protein, humanInterleukin-10NFATC1 protein, humanNFATC Transcription FactorsReceptors, Antigen, B-CellSTAT3 protein, humanSTAT3 Transcription Factor

Identifiers

PMID30209121
PMCPMC6634963
OpenAlexW2890493276

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 Socratic graph.