Evidence map›Paper›PMID 39377122›Full record

ReviewCancer science2024

CX3CR1

Jiajin Ma, Yue Wu, Shaoxian Wu, Zhang Fang, Lujun Chen, Jingting Jiang, Xiao Zheng

Abstract readReview
In one paragraph

Review in Cancer science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–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

12 citing papers in PubMed.

  1. Trial
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Inflammatory factors collaboratively linkFrontiers in immunology · 2025
    Review
  11. Review
  12. CX3CR1Cancer science · 2024
    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

7 authors.

Jiajin MaDepartment of Tumor Biological Treatment, The Third Affiliated Hospital of Soochow University, Changzhou, China.ORCID https://orcid.org/0009-0001-1742-4964
Yue WuDepartment of Tumor Biological Treatment, The Third Affiliated Hospital of Soochow University, Changzhou, China.
Shaoxian WuDepartment of Tumor Biological Treatment, The Third Affiliated Hospital of Soochow University, Changzhou, China.
Zhang FangDepartment of Tumor Biological Treatment, The Third Affiliated Hospital of Soochow University, Changzhou, China.
Lujun ChenDepartment of Tumor Biological Treatment, The Third Affiliated Hospital of Soochow University, Changzhou, China.
Jingting JiangDepartment of Tumor Biological Treatment, The Third Affiliated Hospital of Soochow University, Changzhou, China.ORCID https://orcid.org/0000-0002-3128-9762
Xiao ZhengDepartment of Tumor Biological Treatment, The Third Affiliated Hospital of Soochow University, Changzhou, China.

Funding

Changzhou International Cooperation Project CZ20210035Changzhou Medical Center of Nanjing Medical University CZKYCMCC202202Changzhou Medical Center of Nanjing Medical University CZKYCMCC202301National Natural Science Foundation of China 32270955National Natural Science Foundation of China 82172689the Jiangsu Provincial Medical Key Discipline YXZDXK202236the Key Project of Jiangsu Provincial Health Commission K2023069the Key R&D Project of Jiangsu Province BE2022721the Science and Technology Support Plan (Social Development) Project of Changzhou CE20235058
6 · The paper itself

Abstract

CX3CR1 functions as the specific receptor for the chemokine CX3CL1, demonstrating expression across a broad spectrum of immune cells. This underscores its pivotal role in communication and response mechanisms within the immune system. Upon engagement with CX3CL1, CX3CR1 initiates a cascade of downstream signaling pathways that regulate various biological functions. In the context of tumor progression, the intricate and inhibitory nature of the tumor microenvironment presents a significant challenge to current clinical treatment techniques. This review aims to comprehensively explore the tumor-destructive potential shown by CX3CR1

Indexed as

CD8-Positive T-LymphocytesCX3C Chemokine Receptor 1ImmunotherapyNeoplasmsTumor MicroenvironmentAnimalsChemokine CX3CL1HumansSignal TransductionChemokine CX3CL1CX3C Chemokine Receptor 1CX3CL1 protein, humanCX3CR1 protein, humanCD8+ T cellCX3CR1immunotherapytumor microenvironment

Identifiers

PMID39377122
PMCPMC11611776

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.