Evidence map›Paper›PMID 26405609›Full record

ArticleOncoimmunology2015

Particulate β-glucan regulates the immunosuppression of granulocytic myeloid-derived suppressor cells by inhibiting NFIA expression.

Xinyu Tian, Jie Tian, Xinyi Tang, Ke Rui, Yue Zhang, Jie Ma, Yungang Wang, Huaxi Xu, Liwei Lu, Shengjun Wang

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

19 citing papers in PubMed, 30 citations in OpenAlex.

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  3. Journal of immunology research · 2024
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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

10 authors at 2 institutions in 2 countries.

Xinyu TianDepartment of Laboratory Medicine; The Affiliated People's Hospital; Jiangsu University ; Zhenjiang, China ; Institute of Laboratory Medicine; Jiangsu Key Laboratory of Laboratory Medicine; Jiangsu University ; Zhenjiang, China.
Jie TianInstitute of Laboratory Medicine; Jiangsu Key Laboratory of Laboratory Medicine; Jiangsu University ; Zhenjiang, China.
Xinyi TangInstitute of Laboratory Medicine; Jiangsu Key Laboratory of Laboratory Medicine; Jiangsu University ; Zhenjiang, China.
Ke RuiInstitute of Laboratory Medicine; Jiangsu Key Laboratory of Laboratory Medicine; Jiangsu University ; Zhenjiang, China.
Yue ZhangDepartment of Laboratory Medicine; The Affiliated People's Hospital; Jiangsu University ; Zhenjiang, China.
Jie MaInstitute of Laboratory Medicine; Jiangsu Key Laboratory of Laboratory Medicine; Jiangsu University ; Zhenjiang, China.
Yungang WangInstitute of Laboratory Medicine; Jiangsu Key Laboratory of Laboratory Medicine; Jiangsu University ; Zhenjiang, China.
Huaxi XuInstitute of Laboratory Medicine; Jiangsu Key Laboratory of Laboratory Medicine; Jiangsu University ; Zhenjiang, China.
Liwei LuDepartment of Pathology and Centre of Infection and Immunology; The University of Hong Kong ; Hong Kong, China.
Shengjun WangDepartment of Laboratory Medicine; The Affiliated People's Hospital; Jiangsu University ; Zhenjiang, China ; Institute of Laboratory Medicine; Jiangsu Key Laboratory of Laboratory Medicine; Jiangsu University ; Zhenjiang, China.
Jiangsu University · CNUniversity of Hong Kong · HK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myeloid-derived suppressor cells (MDSCs) are a heterogeneous group of cells which comprise two subsets: granulocytic MDSCs (G-MDSCs) and monocytic MDSCs (M-MDSCs). MDSCs involve in tumor-associated immune suppression by remarkably blocking effector T-cell activation and inducing expansion of regulatory T cells in the tumor microenvironment. The treatment that alters the suppression of MDSCs can effectively facilitate the antitumor immune responses. Recently, we showed that the whole β-glucan particles (WGPs) are capable of altering the suppression of MDSCs. However, the regulatory mechanism of MDSCs by WGP remains unknown. In this study, we found that the expression of nuclear factor I-A (NFIA), an integral transcriptional component of myeloid differentiation and lineage commitment, was inhibited by WGP in G-MDSCs. The effect of WGP on expression of NFIA was the c-jun molecule dependent via Dectin-1 pathway

Indexed as

myeloid-derived suppressor cellsnuclear factor I-Atumor immunologyβ-glucan

Identifiers

PMID26405609
PMCPMC4570107
OpenAlexW1536638686

What OpenQuestion 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 OpenQuestion graph.