Evidence map›Paper›PMID 38596253›Full record

ArticleClinical & translational immunology2024

CD177 drives the transendothelial migration of Treg cells enriched in human colorectal cancer.

Shouyu Ke, Yi Lei, Yixian Guo, Feng Xie, Yimeng Yu, Haigang Geng, Yiqing Zhong, Danhua Xu, Xu Liu, Fengrong Yu and 6 more

Open access · goldAbstract read
In one paragraph

Article in Clinical & translational immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

16 authors at 1 institution in 2 countries.

Shouyu KeDepartment of Gastrointestinal Surgery, Ren Ji Hospital Shanghai Jiao Tong University School of Medicine Shanghai China.
Yi LeiCenter for Immune-Related Diseases at Shanghai Institute of Immunology, Department of Respiratory and Critical Care Medicine of Ruijin Hospital, Department of Thoracic Surgery of Ruijin Hospital, Department of Immunology and Microbiology Shanghai Jiao Tong University School of Medicine Shanghai China.
Yixian GuoDepartment of Gastrointestinal Surgery, Ren Ji Hospital Shanghai Jiao Tong University School of Medicine Shanghai China.
Feng XieCenter for Immune-Related Diseases at Shanghai Institute of Immunology, Department of Respiratory and Critical Care Medicine of Ruijin Hospital, Department of Thoracic Surgery of Ruijin Hospital, Department of Immunology and Microbiology Shanghai Jiao Tong University School of Medicine Shanghai China.
Yimeng YuCenter for Immune-Related Diseases at Shanghai Institute of Immunology, Department of Respiratory and Critical Care Medicine of Ruijin Hospital, Department of Thoracic Surgery of Ruijin Hospital, Department of Immunology and Microbiology Shanghai Jiao Tong University School of Medicine Shanghai China.
Haigang GengDepartment of Gastrointestinal Surgery, Ren Ji Hospital Shanghai Jiao Tong University School of Medicine Shanghai China.
Yiqing ZhongDepartment of Gastrointestinal Surgery, Ren Ji Hospital Shanghai Jiao Tong University School of Medicine Shanghai China.
Danhua XuDepartment of Gastrointestinal Surgery, Ren Ji Hospital Shanghai Jiao Tong University School of Medicine Shanghai China.
Xu LiuDepartment of Gastrointestinal Surgery, Ren Ji Hospital Shanghai Jiao Tong University School of Medicine Shanghai China.
Fengrong YuDepartment of Gastrointestinal Surgery, Ren Ji Hospital Shanghai Jiao Tong University School of Medicine Shanghai China.
Xiang XiaDepartment of Gastrointestinal Surgery, Ren Ji Hospital Shanghai Jiao Tong University School of Medicine Shanghai China.
Zizhen ZhangDepartment of Gastrointestinal Surgery, Ren Ji Hospital Shanghai Jiao Tong University School of Medicine Shanghai China.
Chunchao ZhuDepartment of Gastrointestinal Surgery, Ren Ji Hospital Shanghai Jiao Tong University School of Medicine Shanghai China.
Wei LingDepartment of Gastrointestinal Surgery, Ren Ji Hospital Shanghai Jiao Tong University School of Medicine Shanghai China.
Bin LiCenter for Immune-Related Diseases at Shanghai Institute of Immunology, Department of Respiratory and Critical Care Medicine of Ruijin Hospital, Department of Thoracic Surgery of Ruijin Hospital, Department of Immunology and Microbiology Shanghai Jiao Tong University School of Medicine Shanghai China.
Wenyi ZhaoDepartment of Gastrointestinal Surgery, Ren Ji Hospital Shanghai Jiao Tong University School of Medicine Shanghai China.ORCID https://orcid.org/0009-0004-2054-9700
Shanghai Jiao Tong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Regulatory T (Treg) cells regulate immunity in autoimmune diseases and cancers. However, immunotherapies that target tumor-infiltrating Treg cells often induce unwanted immune responses and tissue inflammation. Our research focussed on exploring the expression pattern of CD177 in tumor-infiltrating Treg cells with the aim of identifying a potential target that can enhance immunotherapy effectiveness. Methods: Single-cell RNA sequencing (scRNA-seq) data and survival data were obtained from public databases. Twenty-one colorectal cancer patient samples, including fresh tumor tissues, peritumoral tissues and peripheral blood mononuclear cells (PBMCs), were analysed using flow cytometry. The transendothelial activity of CD177 Results: ScRNA-seq and flow cytometry results indicated that CD177 was exclusively expressed in intratumoral Treg cells. CD177 Conclusions: These results demonstrated that Treg cells with higher CD177 levels exhibited an enhanced activation status and transendothelial migration capacity. Our findings suggest that CD177 may serve as an immunotherapeutic target and that overexpression of CD177 may improve the efficacy of chimeric antigen receptor T (CAR-T) cell therapy.

Indexed as

CD177migrationregulatory T cellstumor microenvironment

Identifiers

PMID38596253
PMCPMC11003710
OpenAlexW4394627485

What OpenQuestion holds

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Registered trials

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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.