Evidence map›Paper›PMID 33175182›Full record

ArticleCancer immunology, immunotherapy : CII2021

The M1/M2 spectrum and plasticity of malignant pleural effusion-macrophage in advanced lung cancer.

Ming-Fang Wu, Chih-An Lin, Tzu-Hang Yuan, Hsiang-Yuan Yeh, Sheng-Fang Su, Chin-Lin Guo, Gee-Chen Chang, Ker-Chau Li, Chao-Chi Ho, Huei-Wen Chen

Open access · hybridAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 11% 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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 46 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. CXCL2/CXCR2 pathway regulates CD169Frontiers in medicine · 2026
    Article
  6. Review
  7. Periplosides Extract fromCurrent issues in molecular biology · 2024
    Article
  8. Article
  9. Article
  10. Article
  11. Complement C1q is a key player in tumor-associated macrophage-mediated CD8International journal of biological sciences · 2024
    Article
  12. C1qJournal for immunotherapy of cancer · 2023
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. 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

10 authors at 6 institutions in 2 countries.

Ming-Fang Wu *Graduate Institute of Toxicology, College of Medicine, National Taiwan University, No.1, Section 4, Ren-Ai Rd, Taipei, 100, Taiwan.
Chih-An Lin *Department of Internal Medicine, National Taiwan University Hospital and National Taiwan University College of Medicine, No. 7 Chung-Shan South Road, Taipei, 100, Taiwan.
Tzu-Hang YuanGraduate Institute of Toxicology, College of Medicine, National Taiwan University, No.1, Section 4, Ren-Ai Rd, Taipei, 100, Taiwan.
Hsiang-Yuan YehSchool of Big Data Management, Soochow University, Taipei, Taiwan.
Sheng-Fang SuGraduate Institute of Oncology, National Taiwan University College of Medicine, Taipei, Taiwan.
Chin-Lin GuoInstitute of Physics, Academia Sinica, Taipei, Taiwan.
Gee-Chen ChangDivision of Chest Medicine, Department of Internal Medicine, Taichung Veterans General Hospital, Taichung, Taiwan.
Ker-Chau LiInstitute of Statistical Sciences, Academia Sinica, Taipei, Taiwan.
Chao-Chi HoDepartment of Internal Medicine, National Taiwan University Hospital and National Taiwan University College of Medicine, No. 7 Chung-Shan South Road, Taipei, 100, Taiwan. ccho1203@ntu.edu.tw.
Huei-Wen ChenGraduate Institute of Toxicology, College of Medicine, National Taiwan University, No.1, Section 4, Ren-Ai Rd, Taipei, 100, Taiwan. shwchen@ntu.edu.tw.ORCID http://orcid.org/0000-0001-5051-9896
National Taiwan University · TWNational Taiwan University Hospital · TWInstitute of Physics, Academia Sinica · TWNational Yang Ming Chiao Tung University · TWSoochow University · TWUniversity of California, Los Angeles · US

Funding

Academia Sinica AS-SUMMIT-108Ministry of Science and Technology, Taiwan 107-2314-B-002-244-MY3Ministry of Science and Technology, Taiwan 107-2627-M-002-001-Ministry of Science and Technology, Taiwan 108-2321-B-038-003Ministry of Science and Technology, Taiwan 108-3114-Y-001-002
6 · The paper itself

Abstract

backgroundMalignant pleural effusion (MPE)-macrophage (Mφ) of lung cancer patients within unique M1/M2 spectrum showed plasticity in M1-M2 transition. The M1/M2 features of MPE-Mφ and their significance to patient outcomes need to be clarified; furthermore, whether M1-repolarization could benefit treatment remains unclear.

methodsTotal 147 stage-IV lung adenocarcinoma patients undergoing MPE drainage were enrolled for profiling and validation of their M1/M2 spectrum. In addition, the MPE-Mφ signature on overall patient survival was analyzed. The impact of the M1-polarization strategy of patient-derived MPE-Mφ on anti-cancer activity was examined.

resultsWe found that MPE-Mφ expressed both traditional M1 (HLA-DRA) and M2 (CD163) markers and showed a wide range of M1/M2 spectrum. Most of the MPE-Mφ displayed diverse PD-L1 expression patterns, while the low PD-L1 expression group was correlated with higher levels of IL-10. Among these markers, we identified a novel two-gene MPE-Mφ signature, IL-1β and TGF-β1, representing the M1/M2 tendency, which showed a strong predictive power in patient outcomes in our MPE-Mφ patient cohort (N = 60, p = 0.013) and The Cancer Genome Atlas Lung Adenocarcinoma dataset (N = 478, p < 0.0001). Significantly, β-glucan worked synergistically with IFN-γ to reverse the risk signature by repolarizing the MPE-Mφ toward the M1 pattern, enhancing anti-cancer activity.

conclusionsWe identified MPE-Mφ on the M1/M2 spectrum and plasticity and described a two-gene M1/M2 signature that could predict the outcome of late-stage lung cancer patients. In addition, we found that "re-education" of these MPE-Mφ toward anti-cancer M1 macrophages using clinically applicable strategies may overcome tumor immune escape and benefit anti-cancer therapies.

Indexed as

Biomarkers, TumorCell DifferentiationCell PlasticityCells, CulturedGene Expression Regulation, NeoplasticHumansInterleukin-1betaLung NeoplasmsMacrophagesNeoplasm StagingPleural Effusion, MalignantTh1 CellsTh2 CellsTranscriptomeTransforming Growth Factor beta1Biomarkers, TumorInterleukin-1betaTransforming Growth Factor beta1Lung cancerMacrophagesMalignant pleural effusion

Identifiers

PMID33175182
PMCPMC8053174
OpenAlexW3105687100

What OpenQuestion 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 OpenQuestion graph.