Evidence map›Paper›PMID 34933280›Full record

ArticleGut and liver2022

CD40 Agonists Alter the Pancreatic Cancer Microenvironment by Shifting the Macrophage Phenotype toward M1 and Suppress Human Pancreatic Cancer in Organotypic Slice Cultures.

Chae Yoon Lim, Jae Hyuck Chang, Won Sun Lee, Jeana Kim, Il Young Park

Open access · diamondAbstract read
In one paragraph

Article in Gut and liver, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.7field-weighted citation impact, top 7% 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

30 citing papers in PubMed, 45 citations in OpenAlex.

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  12. Macrophages at the Crossroads of Chronic Stress and Cancer.International journal of molecular sciences · 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

5 authors at 1 institution in 1 country.

Chae Yoon LimInstitute of Clinical Medicine Research, The Catholic University of Korea, Seoul, Korea.ORCID 0000-0001-9645-1030
Jae Hyuck ChangDepartment of Internal Medicine, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID 0000-0003-1180-2693
Won Sun LeeInstitute of Clinical Medicine Research, The Catholic University of Korea, Seoul, Korea.ORCID 0000-0003-3043-0071
Jeana KimDepartment of Hospital Pathology, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID 0000-0003-1021-0290
Il Young ParkDepartment of Surgery, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID 0000-0003-4590-2297
Catholic University of Korea · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background/Aims: CD40 agonists are thought to generate antitumor effects on pancreatic cancer via macrophages and T cells. We aimed to investigate the role of CD40 agonists in the differentiation of macrophages and treatment of human pancreatic adenocarcinoma. Methods: Immunohistochemistry was performed on paraffin-embedded surgical blocks from patients with pancreatic cancers to evaluate macrophage phenotypes and their relationship with survival. The effects of CD40 agonists on macrophage phenotypes and human pancreatic cancer were evaluated utilizing cell cocultures and organotypic slice cultures. Results: CD163 Conclusions: CD163 is related to advanced human pancreatic cancer stages and shorter overall survival. CD40 agonists alter macrophage phenotype polarization to favor the M1 phenotype and suppress human pancreatic cancer.

Indexed as

AdenocarcinomaPancreatic NeoplasmsHumansMacrophagesPhenotypeTumor MicroenvironmentCD163 antigenCD40 immunoglobulinMacrophagesPancreatic neoplasmTumor microenvironment

Identifiers

PMID34933280
PMCPMC9289829
OpenAlexW4200089385

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.