Evidence map›Paper›PMID 27095576›Full record

ReviewOncotarget2016

GARP: a surface molecule of regulatory T cells that is involved in the regulatory function and TGF-β releasing.

Liping Sun, Hao Jin, Hui Li

Open access · diamondAbstract readReview
In one paragraph

Review in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

41 citing papers in PubMed, 65 citations in OpenAlex.

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  14. CD4Frontiers in immunology · 2023
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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

3 authors at 2 institutions in 1 country.

Liping SunDepartment of Immunology, Tianjin Medical University Cancer Institute and Hospital, Tianjin, China.
Hao JinDepartment of Immunology, Tianjin Medical University Cancer Institute and Hospital, Tianjin, China.
Hui LiDepartment of Gastrointestinal Cancer Biology, Tianjin Medical University Cancer Institute and Hospital, Tianjin, China.
Tianjin Medical University Cancer Institute and Hospital · CNNational Clinical Research Center for Digestive Diseases · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There are many molecules that define regulatory T cells (Tregs) phenotypically and functionally. Glycoprotein A repetitions predominant (GARP) is a transmembrane protein containing leucine rich repeats. Recently, GARP is found to express highly on the surface of activated Tregs. The combination of GARP and other surface molecules isolates Tregs with higher purity. Besides, GARP is a cell surface molecule of Tregs that maintains their regulatory function and homeosatsis. GARP has also been proved to promote the activation and secretion of transforming growth factor β (TGF-β). Moreover, its potential value in cancer immunotherapy is also discussed in this work.

Indexed as

AnimalsCD4-Positive T-LymphocytesCell MembraneForkhead Transcription FactorsGene Expression ProfilingGene Expression RegulationGlycoproteinsHomeostasisHumansImmunotherapyLymphocyte ActivationMembrane ProteinsMiceNeoplasmsT-Lymphocytes, RegulatoryTransforming Growth Factor betaForkhead Transcription FactorsGlycoproteinsLRRC32 protein, humanMembrane ProteinsTransforming Growth Factor betaTransforming Growth Factor beta1glycoprotein A repetitions predominantregulatory T cellstransforming growth factor β

Identifiers

PMID27095576
PMCPMC5173174
OpenAlexW2341575884

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.