Evidence map›Paper›PMID 36660648›Full record

ArticleAnnals of translational medicine2022

M2-TAMs promote immunoresistance in lung adenocarcinoma by enhancing

Lige Wu, Daoan Cheng, Xin Yang, Weiqing Zhao, Cheng Fang, Rui Chen, Mei Ji

Open access · diamondAbstract read
In one paragraph

Article in Annals of translational medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
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  5. Article
  6. Review
  7. The therapeutic potential of RNA m(6)A in lung cancer.Cell communication and signaling : CCS · 2024
    Review
  8. Review
  9. Review
  10. The RNA mFrontiers in immunology · 2024
    Review
  11. Article
  12. Review
  13. mFrontiers in immunology · 2023
    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 at 1 institution in 1 country.

Lige WuDepartment of Oncology, The Third Affiliated Hospital of Soochow University, Changzhou, China.
Daoan ChengDepartment of Oncology, The Third Affiliated Hospital of Soochow University, Changzhou, China.
Xin YangDepartment of Oncology, The Third Affiliated Hospital of Soochow University, Changzhou, China.
Weiqing ZhaoDepartment of Oncology, The Third Affiliated Hospital of Soochow University, Changzhou, China.
Cheng FangDepartment of Oncology, The Third Affiliated Hospital of Soochow University, Changzhou, China.
Rui ChenDepartment of Oncology, The Third Affiliated Hospital of Soochow University, Changzhou, China.
Mei JiDepartment of Oncology, The Third Affiliated Hospital of Soochow University, Changzhou, China.
Soochow University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Immunotherapy has become the first-line treatment for advanced non-small-cell lung cancer (NSCLC), but most patients still fail to benefit or have disease progression following treatment. M2 phenotype tumor-associated macrophages (M2-TAMs) are important cellular components in the immunosuppressive microenvironment of NSCLC, but how they contribute to immunoresistance remains unclear. This study was conducted to investigate the role and mechanism of M2-TAMs in NSCLC immunoresistance. Methods: We collected postoperative tumor samples for detection of M2-TAMs and other immune cells infiltration by immunofluorescence detection and flow cytometry. We then constructed a non-contact cell co-culture system using Transwell chambers. CCK-8, colony formation, wound healing and invasion assays were performed to evaluated the effect of M2-TAMs on the proliferation, migration and invasion abilities of lung adenocarcinoma (LUAD) cells Results: M2-TAMs were greatly increased in the tumor tissue of patients with immunoresistant LUAD. They could significantly promote the proliferation, invasion, and migration of LUAD cells, and improve their resistance to cytotoxic T lymphocytes (CTL) cytotoxicity. Further research showed M2-TAMs could considerably enhance the expression of Conclusions: In conclusion, M2-TAMs could promote LUAD immunoresistance by enhancing

Indexed as

immunoresistanceM2 phenotype tumor-associated macrophages (M2-TAMs)METTL3non-small cell lung cancer (NSCLC)

Identifiers

PMID36660648
PMCPMC9843413
OpenAlexW4313363844

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.