Evidence map›Paper›PMID 39636298›Full record

ArticleThe Journal of experimental medicine2025

Tumor-associated neutrophils attenuate the immunosensitivity of hepatocellular carcinoma.

Jia Ming Nickolas Teo, Zhulin Chen, Weixin Chen, Rachael Julia Yuenyinn Tan, Qi Cao, Yingming Chu, Delin Ma, Liting Chen, Huajian Yu, Ka-Hei Lam and 8 more

Abstract read
In one paragraph

Article in The Journal of experimental medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Article
  2. Review
  3. Neutrophils in cancer.Nature reviews. Cancer · 2026
    Review
  4. Article
  5. Review
  6. Article
  7. Reinvigorating COTL1Nature cell biology · 2026
    Article
  8. Review
  9. FAPαAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. Review
  17. Review
  18. Respiratory viral infections prime accelerated lung cancer growth.bioRxiv : the preprint server for biology · 2025
    Article
  19. Beyond the Limit: MYC Mediates Tumor Immune Escape.Pharmaceuticals (Basel, Switzerland) · 2025
    Review
  20. Article
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

18 authors.

Jia Ming Nickolas TeoSchool of Biomedical Sciences, Li Ka Shing Faculty of Medicine, The University of Hong Kong , Hong Kong, China.ORCID 0000-0003-3831-5860
Zhulin ChenSchool of Biomedical Sciences, Li Ka Shing Faculty of Medicine, The University of Hong Kong , Hong Kong, China.ORCID 0009-0005-8687-7181
Weixin ChenSchool of Biomedical Sciences, Li Ka Shing Faculty of Medicine, The University of Hong Kong , Hong Kong, China.ORCID 0000-0001-7633-5489
Rachael Julia Yuenyinn TanSchool of Biomedical Sciences, Li Ka Shing Faculty of Medicine, The University of Hong Kong , Hong Kong, China.ORCID 0009-0003-9001-179X
Qi CaoYunnan Baiyao International Medical Research Center, Peking University , Beijing, China.ORCID 0000-0001-6571-0095
Yingming ChuYunnan Baiyao International Medical Research Center, Peking University , Beijing, China.ORCID 0000-0003-2074-5651
Delin MaDepartment of Hepatobiliary Surgery, Peking University People's Hospital, Beijing Key Surgical Basic Research Laboratory of Liver Cirrhosis and Liver Cancer, Beijing, China.ORCID 0000-0001-6886-9886
Liting ChenYunnan Baiyao International Medical Research Center, Peking University , Beijing, China.ORCID 0009-0009-4298-702X
Huajian YuSchool of Biomedical Sciences, Li Ka Shing Faculty of Medicine, The University of Hong Kong , Hong Kong, China.ORCID 0000-0002-2337-2443
Ka-Hei LamSchool of Biomedical Sciences, Li Ka Shing Faculty of Medicine, The University of Hong Kong , Hong Kong, China.ORCID 0000-0003-2103-9396
Terence Kin Wah LeeDepartment of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hong Kong, China.ORCID 0000-0003-0682-322X
Svetoslav ChakarovShanghai Institute of Immunology, Shanghai Jiao Tong University School of Medicine , Shanghai, China.ORCID 0000-0002-0665-5417
Burkhard BecherInstitue of Experimental Immunology, University of Zurich , Zurich, Switzerland.ORCID 0000-0002-1541-7867
Ning ZhangYunnan Baiyao International Medical Research Center, Peking University , Beijing, China.ORCID 0000-0001-7182-0100
Zhao LiDepartment of Hepatobiliary Surgery, Peking University People's Hospital, Beijing Key Surgical Basic Research Laboratory of Liver Cirrhosis and Liver Cancer, Beijing, China.ORCID 0000-0003-0512-2835
Stephanie MaSchool of Biomedical Sciences, Li Ka Shing Faculty of Medicine, The University of Hong Kong , Hong Kong, China.ORCID 0000-0002-2029-7943
Ruidong XueYunnan Baiyao International Medical Research Center, Peking University , Beijing, China.ORCID 0000-0002-5743-805X
Guang Sheng LingSchool of Biomedical Sciences, Li Ka Shing Faculty of Medicine, The University of Hong Kong , Hong Kong, China.ORCID 0000-0002-6347-0005

Funding

Beijing Municipal Natural Science Foundation Z240016Beijing Nova Program 20230434854Croucher FoundationGeneral Research Fund 17116622Innovation and Technology CommissionNational Key Research and Development Project of China 2022YFC3400902National Natural Science Foundation of China 82322047Peking University PKU2024LCXQ002Research Grants Council RFS2122-7S05Research Grants Council of Hong Kong 27118520Research Grants Council Research Impact Fund R7022-20RGC Theme-based research scheme T12-705/24-R
6 · The paper itself

Abstract

Tumor-associated neutrophils (TANs) are heterogeneous; thus, their roles in tumor development could vary depending on the cancer type. Here, we showed that TANs affect metabolic dysfunction-associated steatohepatitis hepatocellular carcinoma (MASH-related HCC) more than viral-associated HCC. We attributed this difference to the predominance of SiglecFhi TANs in MASH-related HCC tumors. Linoleic acid and GM-CSF, which are commonly elevated in the MASH-related HCC microenvironment, fostered the development of this c-Myc-driven TAN subset. Through TGFβ secretion, SiglecFhi TANs promoted HCC stemness, proliferation, and migration. Importantly, SiglecFhi TANs supported immune evasion by directly suppressing the antigen presentation machinery of tumor cells. SiglecFhi TAN removal increased the immunogenicity of a MASH-related HCC model and sensitized it to immunotherapy. Likewise, a high SiglecFhi TAN signature was associated with poor prognosis and immunotherapy resistance in HCC patients. Overall, our study highlights the importance of understanding TAN heterogeneity in cancer to improve therapeutic development.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsNeutrophilsTumor MicroenvironmentAnimalsCell Line, TumorCell ProliferationGranulocyte-Macrophage Colony-Stimulating FactorHumansImmunotherapyLinoleic AcidMaleMiceMice, Inbred C57BLTransforming Growth Factor betaGranulocyte-Macrophage Colony-Stimulating FactorLinoleic AcidTransforming Growth Factor beta

Identifiers

PMID39636298
PMCPMC11619716

What OpenQuestion holds

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LicenceCC BY-NC-SA
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.