Evidence map›Paper›PMID 38919615›Full record

ReviewFrontiers in immunology2024

Advances in Foxp3+ regulatory T cells (Foxp3+ Treg) and key factors in digestive malignancies.

Wanyao Wang, Minglu Ding, Qiuhong Wang, Yidan Song, Keyuan Huo, Xiaojie Chen, Zihan Xiang, Lantao Liu

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

9 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. 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

8 authors.

Wanyao WangSchool of Basic Medicine, Mudanjiang Medical University, Mudanjiang, Heilongjiang, China.
Minglu DingMudanjiang Medical University, Mudanjiang, Heilongjiang, China.
Qiuhong WangMudanjiang Hospital for Cardiovascular Diseases, Department of Anesthesiology, Mudanjiang, Heilongjiang, China.
Yidan SongSchool of Basic Medicine, Mudanjiang Medical University, Mudanjiang, Heilongjiang, China.
Keyuan HuoSchool of Basic Medicine, Mudanjiang Medical University, Mudanjiang, Heilongjiang, China.
Xiaojie ChenSchool of Basic Medicine, Mudanjiang Medical University, Mudanjiang, Heilongjiang, China.
Zihan XiangSchool of Basic Medicine, Mudanjiang Medical University, Mudanjiang, Heilongjiang, China.
Lantao LiuSchool of Basic Medicine, Mudanjiang Medical University, Mudanjiang, Heilongjiang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Foxp3+ regulatory T cells (Foxp3+ Treg) play a role in regulating various types of tumors, but uncertainty still exists regarding the exact mechanism underlying Foxp3+ Treg activation in gastrointestinal malignancies. As of now, research has shown that Foxp3+ Treg expression, altered glucose metabolism, or a hypoxic tumor microenvironment all affect Foxp3+ Treg function in the bodies of tumor patients. Furthermore, it has been demonstrated that post-translational modifications are essential for mature Foxp3 to function properly. Additionally, a considerable number of non-coding RNAs (ncRNAs) have been implicated in the activation of the Foxp3 signaling pathway. These mechanisms regulating Foxp3 may one day serve as potential therapeutic targets for gastrointestinal malignancies. This review primarily focuses on the properties and capabilities of Foxp3 and Foxp3+Treg. It emphasizes the advancement of research on the regulatory mechanisms of Foxp3 in different malignant tumors of the digestive system, providing new insights for the exploration of anticancer treatments.

Indexed as

Forkhead Transcription FactorsT-Lymphocytes, RegulatoryTumor MicroenvironmentAnimalsDigestive System NeoplasmsGastrointestinal NeoplasmsHumansSignal TransductionForkhead Transcription FactorsFOXP3 protein, humandigestive system malignanciesFoxp3FOXP3+ regulatory T cellsFoxp3 transcriptional and post-translational modificationsimmunotherapy targeting Foxp3+Treg

Identifiers

PMID38919615
PMCPMC11196412

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.