Evidence map›Paper›PMID 41184283›Full record

ReviewCell death & disease2025

Oncogenic KRAS mutations drive immune suppression through immune-related regulatory network and metabolic reprogramming.

Lin Tian, Hui Li, Heran Cui, Chenchen Tang, Peiyan Zhao, Xinyue Wang, Ying Cheng

Abstract readReview
In one paragraph

Review in Cell death & disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. RAS-targeted therapies for pancreatic cancer.ESMO gastrointestinal oncology · 2026
    Review
  2. Review
  3. Review
  4. Targeted therapeutic strategies forTranslational lung cancer research · 2026
    Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. UnlockingCurrent oncology (Toronto, Ont.) · 2026
    Review
  11. Review
  12. Article
  13. Review
  14. Review
  15. Divergent CD45Frontiers in immunology · 2026
    Article
  16. Review
  17. 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.

Lin TianMedical Oncology Translational Research Lab, Jilin Cancer Hospital, Changchun, China.
Hui LiMedical Oncology Translational Research Lab, Jilin Cancer Hospital, Changchun, China.
Heran CuiBiobank, Jilin Cancer Hospital, Changchun, China.
Chenchen TangBiobank, Jilin Cancer Hospital, Changchun, China.
Peiyan ZhaoMedical Oncology Translational Research Lab, Jilin Cancer Hospital, Changchun, China.
Xinyue WangPostdoctoral Research Workstation, Jilin Cancer Hospital, Changchun, China.
Ying ChengMedical Oncology Translational Research Lab, Jilin Cancer Hospital, Changchun, China. chengying@csco.org.cn.ORCID http://orcid.org/0000-0001-9908-597X

Funding

Jilin Department of Health (Department of Health, Jilin Province) 2023JC60Natural Science Foundation of Jilin Province (Natural Science Foundation of Jilin Province of China) YDZJ202201ZYTS146
6 · The paper itself

Abstract

The KRAS mutation represents the most prevalent oncogenic alteration observed in human cancers. Its primary role involves directly driving malignant tumor development and growth through the activation of downstream signaling pathways. Increasing evidence suggests that KRAS significantly affects the immune response of KRAS-mutant tumors by modulating immune-related signaling and inflammatory pathways. In addition to broadly regulating the KRAS-associated immune signaling, KRAS influences immune cell phenotype and function by triggering tumor metabolic pathways. Here, we reviewed the KRAS mutation-associated immune microenvironment features and discussed how KRAS remodels the immune microenvironment by regulating immune-related molecules, inflammatory factors, and multiple metabolic pathways, offering insights that could be useful for developing effective immune-responsive therapies for KRAS-mutant tumors.

Indexed as

MutationNeoplasmsProto-Oncogene Proteins p21(ras)AnimalsHumansMetabolic ReprogrammingSignal TransductionTumor MicroenvironmentKRAS protein, humanProto-Oncogene Proteins p21(ras)

Identifiers

PMID41184283
PMCPMC12583504

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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.