Evidence map›Paper›PMID 32680511›Full record

ReviewMolecular cancer2020

Regulatory T cells in tumor microenvironment: new mechanisms, potential therapeutic strategies and future prospects.

Chunxiao Li, Ping Jiang, Shuhua Wei, Xiaofei Xu, Junjie Wang

Open access · goldAbstract readReview
In one paragraph

Review in Molecular cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 635 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
635citing papers in PubMed, 2 pooled it
34.9field-weighted citation impact, top 1% 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

635 citing papers in PubMed, 2 syntheses or guidelines pooled it, 878 citations in OpenAlex.

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  18. Potentiating mild photothermal therapy via CDK12/13-mediated AKT suppression to orchestrate ferroptosis-apoptosis crosstalk for vaccine-like immunity.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
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575 more citing papers are in PubMed but not listed here.

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 2 countries.

Chunxiao LiDepartment of Radiation Oncology, Peking University Third Hospital, Beijing, 100191, China. chunxiaoli@pku.edu.cn.ORCID 0000-0002-1805-140X
Ping JiangDepartment of Radiation Oncology, Peking University Third Hospital, Beijing, 100191, China.
Shuhua WeiDepartment of Radiation Oncology, Peking University Third Hospital, Beijing, 100191, China.
Xiaofei XuCenter for Reproductive Medicine, Department of Obstetrics and Gynecology, Peking University Third Hospital, Beijing, 100191, China.
Junjie WangDepartment of Radiation Oncology, Peking University Third Hospital, Beijing, 100191, China. junjiewang_edu@sina.cn.
Peking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Regulatory T cells (Tregs) characterized by the expression of the master transcription factor forkhead box protein p3 (Foxp3) suppress anticancer immunity, thereby hindering protective immunosurveillance of tumours and hampering effective antitumour immune responses in tumour-bearing hosts, constitute a current research hotspot in the field. However, Tregs are also essential for the maintenance of the immune tolerance of the body and share many molecular signalling pathways with conventional T cells, including cytotoxic T cells, the primary mediators of tumour immunity. Hence, the inability to specifically target and neutralize Tregs in the tumour microenvironment without globally compromising self-tolerance poses a significant challenge. Here, we review recent advances in characterizing tumour-infiltrating Tregs with a focus on the functional roles of costimulatory and inhibitory receptors in Tregs, evaluate their potential as clinical targets, and systematically summarize their roles in potential treatment strategies. Also, we propose modalities to integrate our increasing knowledge on Tregs phenotype and function for the rational design of checkpoint inhibitor-based combination therapies. Finally, we propose possible treatment strategies that can be used to develop Treg-targeted therapies.

Indexed as

AnimalsDisease ManagementDisease SusceptibilityEnergy MetabolismGene Expression Regulation, NeoplasticHumansImmunomodulationImmunotherapyMolecular Targeted TherapyNeoplasmsT-Lymphocytes, RegulatoryT-Lymphocyte SubsetsTumor Microenvironment

Identifiers

PMID32680511
PMCPMC7367382
OpenAlexW3042467660

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.