Evidence map›Paper›PMID 38528665›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2024

The Dual Role of the NFATc2/galectin-9 Axis in Modulating Tumor-Initiating Cell Phenotypes and Immune Suppression in Lung Adenocarcinoma.

Zhi-Jie Xiao, Si-Qi Wang, Jun-Jiang Chen, Yun Li, Yuchen Jiang, Vicky Pui-Chi Tin, Jia Liu, Huiyi Hu, Maria Pik Wong, Yihang Pan and 1 more

Open access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.9field-weighted citation impact, top 15% of its field
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

9 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Galectin-9-An Emerging Glyco-Immune Checkpoint Target for Cancer Therapy.International journal of molecular sciences · 2025
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. 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

11 authors at 3 institutions in 2 countries.

Zhi-Jie XiaoScientific Research Centre, The Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen, 518000, China.ORCID 0000-0001-6365-7278
Si-Qi WangDepartment of Pathology, School of Clinical Medicine, The University of Hong Kong, Hong Kong, 999077, Hong Kong.ORCID 0000-0002-7121-2321
Jun-Jiang ChenDepartment of Physiology, School of Medicine, Jinan University, Guangzhou, 510000, China.
Yun LiDepartment of Thoracic Surgery, The Seventh Affiliated Hospital of Sun Yat-Sen University, Shenzhen, China.
Yuchen JiangScientific Research Centre, The Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen, 518000, China.
Vicky Pui-Chi TinDepartment of Pathology, School of Clinical Medicine, The University of Hong Kong, Hong Kong, 999077, Hong Kong.
Jia LiuScientific Research Centre, The Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen, 518000, China.
Huiyi HuScientific Research Centre, The Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen, 518000, China.
Maria Pik WongDepartment of Pathology, School of Clinical Medicine, The University of Hong Kong, Hong Kong, 999077, Hong Kong.
Yihang PanScientific Research Centre, The Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen, 518000, China.
Judy Wai Ping YamDepartment of Pathology, School of Clinical Medicine, The University of Hong Kong, Hong Kong, 999077, Hong Kong.ORCID 0000-0002-5637-121X
Sun Yat-sen University · CNChinese University of Hong Kong · HKJinan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor-initiating cells (TICs) resilience and an immunosuppressive microenvironment are aggressive oncogenic phenotypes that contribute to unsatisfactory long-term outcomes in lung adenocarcinoma (LUAD) patients. The molecular mechanisms mediating the interaction between TICs and immune tolerance have not been elucidated. The role of Galectin-9 in oncogenesis and immunosuppressive microenvironment is still unknown. This study explored the potential role of galectin-9 in TIC regulation and immune modulation in LUAD. The results show that galectin-9 supports TIC properties in LUAD. Co-culture of patient-derived organoids and matched peripheral blood mononuclear cells showed that tumor-secreted galectin-9 suppressed T cell cytotoxicity and induced regulatory T cells (Tregs). Clinically, galectin-9 is upregulated in human LUAD. High expression of galectin-9 predicted poor recurrence-free survival and correlated with high levels of Treg infiltration. LGALS9, the gene encoding galectin-9, is found to be transcriptionally regulated by the nuclear factor of activated T cells 2 (NFATc2), a previously reported TIC regulator, via in silico prediction and luciferase reporter assays. Overall, the results suggest that the NFATc2/galectin-9 axis plays a dual role in TIC regulation and immune suppression.

Indexed as

Adenocarcinoma of LungGalectinsLung NeoplasmsNeoplastic Stem CellsNFATC Transcription FactorsCell Line, TumorHumansPhenotypeTumor MicroenvironmentGalectinsLGALS9 protein, humanNFATC2 protein, humanNFATC Transcription Factorsgalectin‐9immunelung adenocarcinomaNFATc2tumor‐initiating cells

Identifiers

PMID38528665
PMCPMC11132051
OpenAlexW4393197121

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.