Evidence map›Paper›PMID 28496056›Full record

ArticleJournal of clinical and experimental hematopathology : JCEH2017

Stat3 inhibitor abrogates the expression of PD-1 ligands on lymphoma cell lines.

Chaoya Ma, Hasita Horlad, Cheng Pan, Hiromu Yano, Koji Ohnishi, Yukio Fujiwara, Masao Matsuoka, Aeju Lee, Takuro Niidome, Ryuya Yamanaka and 2 more

Abstract read
In one paragraph

Article in Journal of clinical and experimental hematopathology : JCEH, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

16 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  15. Potential anti-lymphoma effect of M-CSFR inhibitor in adult T-cell leukemia/lymphoma.Journal of clinical and experimental hematopathology : JCEH · 2018
    Article
  16. SARS-CoV-2-related immune dysregulation and biologically plausible pathways to lymphomagenesis: a PRISMA-ScR-based scoping review.Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie
    Article
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.

Chaoya MaDepartment of Cell Pathology, Graduate School of Medical Sciences, Kumamoto University.
Hasita HorladDepartment of Cell Pathology, Graduate School of Medical Sciences, Kumamoto University.
Cheng PanDepartment of Cell Pathology, Graduate School of Medical Sciences, Kumamoto University.
Hiromu YanoDepartment of Cell Pathology, Graduate School of Medical Sciences, Kumamoto University.
Koji OhnishiDepartment of Cell Pathology, Graduate School of Medical Sciences, Kumamoto University.
Yukio FujiwaraDepartment of Cell Pathology, Graduate School of Medical Sciences, Kumamoto University.
Masao MatsuokaDepartment of Hematology, Graduate School of Medical Sciences, Kumamoto University.
Aeju LeeInternational Research Organization for Advanced Science and Technology (IROAST), Kumamoto University.
Takuro NiidomeFaculty of Advanced Science and Technology, Kumamoto University.
Ryuya YamanakaKyoto Prefectural University of Medicine, Graduate School for Health Care Science.
Motohiro TakeyaDepartment of Cell Pathology, Graduate School of Medical Sciences, Kumamoto University.
Yoshihiro KomoharaDepartment of Cell Pathology, Graduate School of Medical Sciences, Kumamoto University.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent studies have indicated the significance of immune checkpoint molecules including programmed death-1 (PD-1), cytotoxic T-lymphocyte associated protein 4, and T-cell immunoglobulin and mucin domain-containing molecule-3 for anti-tumor immune responses. We previously investigated PD-1 ligand 1/2 (PD-L1/2) expression in lymphoma cell lines, and found that PD-L1/2 is expressed on the adult T-cell leukemia/lymphoma (ATL-T) and B-cell lymphoma (SLVL) cell lines. In the present study, we investigated whether the Stat3 inhibitor WP1066 abrogated PD-L1/2 expression in lymphoma cell lines. Incubation with WP1066 inhibited lymphoma cell growth and induced cell apoptosis. PD-L1/2 expression in the ATL-T, SLVL, and human brain malignant lymphoma (HKBML) cell lines was significantly abrogated by WP1066 treatment. These data indicated that a Stat3 inhibitor abrogated PD-L1/2 expression in lymphoma cells. Such an inhibitor is therefore considered to be useful for additional immunotherapy in patients with advanced lymphoma.

Indexed as

ApoptosisB7-H1 AntigenCaspase 3Cell Line, TumorCell ProliferationDown-RegulationGene Expression Regulation, NeoplasticHumansLymphomaPyridinesSTAT3 Transcription FactorTyrphostinsB7-H1 AntigenCaspase 3PyridinesSTAT3 Transcription FactorTyrphostinsWP1066lymphomaPD-L1PD-L2Stat3

Identifiers

PMID28496056
PMCPMC6144272

What OpenQuestion holds

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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 OpenQuestion graph.