Evidence map›Paper›PMID 41257391›Full record

ArticleInternational journal of cancer2026

C-X-C chemokine receptor CXCR4 mediates diurnal changes in the aggregation and dispersion of CD8

Akito Tsuruta, Marina Fujimoto, Yasuha Hiraoka, Aoi Taniguchi, Yuki Shiiba, Takuto Inoki, Tomoaki Yamauchi, Yuya Yoshida, Naoya Matsunaga, Shigehiro Ohdo and 1 more

Abstract read
In one paragraph

Article in International journal of cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Review
  5. 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

11 authors.

Akito TsurutaDepartment of Pharmaceutics, Faculty of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.ORCID https://orcid.org/0000-0003-0588-0302
Marina FujimotoDepartment of Pharmaceutics, Faculty of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.
Yasuha HiraokaDepartment of Pharmaceutics, Faculty of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.
Aoi TaniguchiDepartment of Pharmaceutics, Faculty of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.
Yuki ShiibaDepartment of Pharmaceutics, Faculty of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.
Takuto InokiDepartment of Pharmaceutics, Faculty of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.
Tomoaki YamauchiDepartment of Pharmaceutics, Faculty of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.ORCID https://orcid.org/0009-0001-2598-4566
Yuya YoshidaDepartment of Clinical Pharmacokinetics, Faculty of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.ORCID https://orcid.org/0000-0003-2394-9748
Naoya MatsunagaDepartment of Clinical Pharmacokinetics, Faculty of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.ORCID https://orcid.org/0000-0002-0004-4535
Shigehiro OhdoDepartment of Clinical Pharmacokinetics, Faculty of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.
Satoru KoyanagiDepartment of Pharmaceutics, Faculty of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.ORCID https://orcid.org/0000-0003-4849-2377

Funding

Japan Agency for Medical Research and Development JP24am121031Japan Society for the Promotion of Science 20K16306Japan Society for the Promotion of Science 21K18249Japan Society for the Promotion of Science 22H00442Japan Society for the Promotion of Science 22K18375Japan Society for the Promotion of Science 23K14569Japan Society for the Promotion of Science 25K02425Japan Society for the Promotion of Science 25K10469
6 · The paper itself

Abstract

Immune checkpoint inhibitors (ICIs) are widely used to treat various types of cancer; however, their effectiveness varies, with some patients exhibiting resistance. Recent studies have shown that the efficacy of ICIs depends on the localization of immune cells, particularly T cells, within the tumor microenvironment (TME). Although the circadian clock is known to regulate immune cell migration into tumors, its role in orchestrating spatially precise intratumoral localization remains unclear. Here, we found that the distribution of CD8

Indexed as

CD8-Positive T-LymphocytesCircadian RhythmLung NeoplasmsReceptors, CXCR4Tumor MicroenvironmentAnimalsCancer-Associated FibroblastsCell Line, TumorCell MovementChemokine CXCL12FemaleGene Expression Regulation, NeoplasticHumansImmune Checkpoint InhibitorsLymphocytes, Tumor-InfiltratingMiceChemokine CXCL12CXCR4 protein, humanImmune Checkpoint InhibitorsReceptors, CXCR4Transforming Growth Factor betacircadian rhythmimmune checkpoint inhibitortumor microenvironment

Identifiers

PMID41257391
PMCPMC12811207

What OpenQuestion holds

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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.