Evidence map›Paper›PMID 37098880›Full record

ArticleEuropean journal of histochemistry : EJH2023

Clinicopathological assessment of PD-1/PD-L1 immune checkpoint expression in desmoid tumors.

Kazuhiko Hashimoto, Shunji Nishimura, Yu Shinyashiki, Tomohiko Ito, Ryosuke Kakinoki, Masao Akagi

Open access · goldAbstract read
In one paragraph

Article in European journal of histochemistry : EJH, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

10 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
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  5. Jingzhi Niuhuangjiedu Tablet Ameliorates Oral MucositisCombinatorial chemistry & high throughput screening · 2025
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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

6 authors at 1 institution in 1 country.

Kazuhiko HashimotoDepartment of Orthopedic Surgery, Kushimoto Municipality Hospital, Wakayama; Department of Orthopedic Surgery, Kindai University Hospital, Osaka-Sayama City, Osaka. hazzhiko@med.kindai.ac.jp.
Shunji NishimuraDepartment of Orthopedic Surgery, Kindai University Hospital, Osaka-Sayama City, Osaka. shunnisi@med.kindai.ac.jp.
Yu ShinyashikiDepartment of Orthopedic Surgery, Kushimoto Municipality Hospital, Wakayama; Department of Orthopedic Surgery, Kindai University Hospital, Osaka-Sayama City, Osaka. shinyashiki@med.kindai.ac.jp.
Tomohiko ItoDepartment of Orthopedic Surgery, Kindai University Hospital, Osaka-Sayama City, Osaka. tomo0251118zooo@gmail.com.
Ryosuke KakinokiDepartment of Orthopedic Surgery, Kindai University Hospital, Osaka-Sayama City, Osaka. rkakinoki@med.kindai.ac.jp.
Masao AkagiDepartment of Orthopedic Surgery, Kindai University Hospital, Osaka-Sayama City, Osaka. makagi@med.kindai.ac.jp.
Kindai University Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The details of immune molecules' expression in desmoid tumors (DTs) remain unclear. This study aimed to determine the expression status of the programmed death-1/programmed death ligand 1 (PD1/PD-L1) immune checkpoint mechanism in DTs. The study included patients with DTs (n=9) treated at our institution between April 2006 and December 2012. Immunostaining for CD4, CD8, PD-1, PD-L1, interleukin-2 (IL-2), and interferon-gamma (IFN-γ) was performed on pathological specimens harvested during the biopsy. The positivity rate of each immune component was calculated as the number of positive cells/total cells. The positivity rate was quantified and correlations between the positivity rates of each immune molecule were also investigated. Immune molecules other than PD-1 were stained in tumor cells and intra-tumor infiltrating lymphocytes. The mean ± SD expression rates of β-catenin, CD4, CD8, PD-1, PD-L1, IL-2, and IFN-ɤ were 43.9±18.9, 14.6±6.80, 0.75±4.70, 0±0, 5.1±6.73, 8.75±6.38, and 7.03±12.1, respectively. The correlation between β-catenin and CD4 was positively moderate (r=0.49); β-catenin and PD-L1, positively weak (r=0.25); CD4 and PD-L1, positively medium (r=0.36); CD8 and IL-2, positively medium (r=0.38); CD8 and IFN-ɤ, positively weak (r=0.28); and IL-2 and IFN-ɤ, positively medium (r=0.36). Our findings suggest that PD-L1-centered immune checkpoint mechanisms may be involved in the tumor microenvironment of DTs.

Indexed as

B7-H1 AntigenDesmoid Tumorsbeta CateninHumansInterleukin-2Programmed Cell Death 1 ReceptorTumor MicroenvironmentB7-H1 Antigenbeta CateninCD274 protein, humanInterleukin-2Programmed Cell Death 1 Receptor

Identifiers

PMID37098880
PMCPMC10184173
OpenAlexW4367047534

What OpenQuestion holds

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LicenceCC BY-NC
Read underepoch 390

Registered trials

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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.