Evidence map›Paper›PMID 35879949›Full record

ArticleJournal of immunology research2022

CXCR2 Is Essential for Radiation-Induced Intestinal Injury by Initiating Neutrophil Infiltration.

Jing Hu, Qian Ji, Fei Chen, Xiaoqin Gong, Chuansheng Chen, Kaijun Zhang, Ye Hua, Jinlei Wang, Rongkun Li, Xu Wang and 2 more

Open access · goldAbstract read
In one paragraph

Article in Journal of immunology research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.5field-weighted citation impact, top 16% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

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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

12 authors at 2 institutions in 1 country.

Jing HuDepartment of Radiation Oncology, The Second Affiliated Hospital of Soochow University, Suzhou 215000, China.ORCID https://orcid.org/0000-0002-1184-3236
Qian JiDepartment of Radiation Oncology, Affiliated Hospital of Jiangsu University, Zhenjiang 212000, China.
Fei ChenDepartment of Radiation Oncology, Affiliated Hospital of Jiangsu University, Zhenjiang 212000, China.
Xiaoqin GongDepartment of Radiation Oncology, Affiliated Hospital of Jiangsu University, Zhenjiang 212000, China.
Chuansheng ChenDepartment of Radiation Oncology, Affiliated Hospital of Jiangsu University, Zhenjiang 212000, China.
Kaijun ZhangDepartment of Radiation Oncology, Affiliated Hospital of Jiangsu University, Zhenjiang 212000, China.
Ye HuaDepartment of Radiation Oncology, Affiliated Hospital of Jiangsu University, Zhenjiang 212000, China.
Jinlei WangDepartment of Radiation Oncology, Affiliated Hospital of Jiangsu University, Zhenjiang 212000, China.
Rongkun LiDepartment of Radiation Oncology, Affiliated Hospital of Jiangsu University, Zhenjiang 212000, China.
Xu WangDepartment of Radiation Oncology, Affiliated Hospital of Jiangsu University, Zhenjiang 212000, China.ORCID https://orcid.org/0000-0002-3768-777X
Chunhua DaiDepartment of Radiation Oncology, Affiliated Hospital of Jiangsu University, Zhenjiang 212000, China.ORCID https://orcid.org/0000-0003-0377-1735
Ye TianDepartment of Radiation Oncology, The Second Affiliated Hospital of Soochow University, Suzhou 215000, China.ORCID https://orcid.org/0000-0001-5295-2263
Jiangsu University · CNSoochow University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neutrophils, known as an important part of the immune system, are the most abundant leukocyte population in peripheral blood, but excessive recruitment will lead to tissue/organ injury. RNA sequencing showed that ionizing radiation significantly increased the expression of characteristic genes of neutrophils in intestinal tissues compared with liver and lung tissues. By clearing neutrophils with an anti-Ly6G antibody, we found that neutrophil infiltration is critical for irradiation-induced intestinal injury. CXCR2 is a G-protein-coupled receptor that mediates the migration of neutrophils by combining with its ligands. Compared with observations in liver and lung tissues, we found that CXCR2 and its ligands, including CXCL1, CXCL2, CXCL3, and CXCL5, were all significantly upregulated in irradiated intestinal tissues. Further studies showed that SB225002, an inhibitor of CXCR2, could effectively inhibit the chemotaxis of neutrophils and tissue damage mediated by the CXCL-CXCR2 signalling pathway.

Indexed as

NeutrophilsReceptors, Interleukin-8BLiverNeutrophil InfiltrationReceptors, Interleukin-8B

Identifiers

PMID35879949
PMCPMC9308512
OpenAlexW4285677575

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.