Evidence map›Paper›PMID 42698854›Full record

ReviewFrontiers in immunology2026

The microbiota-NK cell axis in colorectal cancer: a spatial and subset-centric framework.

Jiexia Wen, Yunhuan Gao, Meimei Xu, Muran Li, Xuetao Dong, Min Zhao, Bin Xuan, Xiangcai Meng, Li He, Weizhi Zhang and 4 more

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

14 authors.

Jiexia Wen *Department of Central Laboratory, The First Hospital of Qinhuangdao, Qinhuangdao, Hebei, China.
Yunhuan Gao *Department of Immunology, Nankai University School of Medicine, Nankai University, Tianjin, China.
Meimei XuDepartment of Gastroenterology, The First Hospital of Qinhuangdao, Qinhuangdao, Hebei, China.
Muran LiDepartment of Gastroenterology, Tianjin Union Medical Center, The First Affiliated Hospital of Nankai University, Tianjin, China.
Xuetao DongDepartment of Gastroenterology, Tianjin Union Medical Center, The First Affiliated Hospital of Nankai University, Tianjin, China.
Min ZhaoDepartment of Pathology, The First Hospital of Qinhuangdao, Qinhuangdao, Hebei, China.
Bin XuanDepartment of General Surgery, The First Hospital of Qinhuangdao, Qinhuangdao, Hebei, China.
Xiangcai MengDepartment of General Surgery, The First Hospital of Qinhuangdao, Qinhuangdao, Hebei, China.
Li HeDepartment of General Surgery, The First Hospital of Qinhuangdao, Qinhuangdao, Hebei, China.
Weizhi ZhangDepartment of General Surgery, The First Hospital of Qinhuangdao, Qinhuangdao, Hebei, China.
Rui LiDepartment of General Surgery, The First Hospital of Qinhuangdao, Qinhuangdao, Hebei, China.
Yang TaoDepartment of Central Laboratory, The First Hospital of Qinhuangdao, Qinhuangdao, Hebei, China.
Fangyizhuo ZhangDepartment of Central Laboratory, The First Hospital of Qinhuangdao, Qinhuangdao, Hebei, China.
Yimin WangDepartment of Central Laboratory, The First Hospital of Qinhuangdao, Qinhuangdao, Hebei, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The gut microbiota and natural killer (NK) cells jointly shape colorectal cancer (CRC) progression and immunotherapy response, yet existing reviews largely adopt a linear, pathogen-centric view that overlooks NK-cell heterogeneity and spatial tumor microenvironment architecture. We propose an integrated framework centered on three progressive pillars: (i) the microbiota appears to selectively shape three well-characterized NK-cell states (activated, dysfunctional, and memory-like), with a fourth regulatory-like state that remains mechanistically uncharacterized through metabolically and genetically mediated mechanisms; (ii) emerging spatial evidence suggests beneficial commensals and activated NK cells preferentially localize to perivascular niches, whereas pathogenic bacteria and dysfunctional NK cells are enriched within the tumor parenchyma, though multicenter validation is needed; and (iii) these insights support two testable patient-stratification strategies for future clinical testing, an "enrichment" approach for tumors with pre-existing activated NK signatures, and a "remodeling" approach for Fusobacterium nucleatum (

Indexed as

Colorectal NeoplasmsGastrointestinal MicrobiomeKiller Cells, NaturalAnimalsHumansTumor Microenvironmentcolorectal cancergut microbiotanatural killer cellsspatial transcriptomicstumor microenvironment

Identifiers

PMID42698854
PMCPMC13542980

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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.