Evidence map›Paper›PMID 34703882›Full record

ArticleMolecular therapy oncolytics2021

Local adenoviral delivery of soluble CD200R-Ig enhances antitumor immunity by inhibiting CD200-β-catenin-driven M2 macrophage.

Seung-Phil Shin, A-Ra Goh, Ji-Min Ju, Hyeon-Gu Kang, Seok-Jun Kim, Jong-Kwang Kim, Eun-Jung Park, Yong-Soo Bae, Kyungho Choi, Yuh-Seog Jung and 1 more

Open access · goldAbstract read
In one paragraph

Article in Molecular therapy oncolytics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
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  7. Emerging Immune Checkpoint Molecules on Cancer Cells: CD24 and CD200.International journal of molecular sciences · 2023
    Review
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

11 authors at 4 institutions in 1 country.

Seung-Phil ShinDivision of Tumor Immunology, Research Institute & Hospital, National Cancer Center, Goyang, Gyeonggi-do 410-769, Republic of Korea.
A-Ra GohDivision of Tumor Immunology, Research Institute & Hospital, National Cancer Center, Goyang, Gyeonggi-do 410-769, Republic of Korea.
Ji-Min JuDivision of Tumor Immunology, Research Institute & Hospital, National Cancer Center, Goyang, Gyeonggi-do 410-769, Republic of Korea.
Hyeon-Gu KangDepartment of Biomedical Science, BK21-Plus Research Team for Bioactive Control Technology, College of Natural Sciences, Chosun University, 309 Pilmun-daero, Dong-gu, Gwangju 61452, Republic of Korea.
Seok-Jun KimDepartment of Biomedical Science, BK21-Plus Research Team for Bioactive Control Technology, College of Natural Sciences, Chosun University, 309 Pilmun-daero, Dong-gu, Gwangju 61452, Republic of Korea.
Jong-Kwang KimGenome Analysis, Team Research Core Center, Research Institute & Hospital, National Cancer Center, Goyang, Republic of Korea.
Eun-Jung ParkDivision of Tumor Immunology, Research Institute & Hospital, National Cancer Center, Goyang, Gyeonggi-do 410-769, Republic of Korea.
Yong-Soo BaeDepartment of Biological Sciences, SRC Center for Immune Research on Non-lymphoid Organs, Sungkyunkwan University, Jangan-gu, Suwon, Republic of Korea.
Kyungho ChoiDepartment of Biochemistry and Molecular Biology, Seoul National University College of Medicine, Seoul, Republic of Korea.
Yuh-Seog JungDivision of Tumor Immunology, Research Institute & Hospital, National Cancer Center, Goyang, Gyeonggi-do 410-769, Republic of Korea.
Sang-Jin LeeDivision of Tumor Immunology, Research Institute & Hospital, National Cancer Center, Goyang, Gyeonggi-do 410-769, Republic of Korea.
National Cancer Center · KRChosun University · KRSeoul National University · KRSungkyunkwan University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CD200 is known as an immune checkpoint molecule that inhibits innate immune cell activation. Using a head and neck squamous cell carcinoma (HNSCC) model, we sought to determine whether localized delivery of adenovirus-expressing sCD200R1-Ig, the soluble extracellular domain of CD200R1, enhances antitumor immunity. Mouse-derived bone marrow cells and M1/M2-like macrophages were cocultured with tumor cells and analyzed for macrophage polarization. As an

Indexed as

CD200M2-like macrophageM-CSFNF-κBPD-L1β-catenin

Identifiers

PMID34703882
PMCPMC8503857
OpenAlexW3199144694

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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 OpenQuestion graph.