Evidence map›Paper›PMID 36482884›Full record

ArticleBreast cancer (Dove Medical Press)2022

Metformin Inducing the Change of Functional and Exhausted Phenotypic Tumor-Infiltrated Lymphocytes and the Correlation with JNK Signal Pathway in Triple-Negative Breast Cancer.

Ruibin Wang, Yuchen Li, Yanjie Zhao, Feng Shi, Quan Zhou, Jiangping Wu, Shuzhen Lyu, Qingkun Song

Open access · goldAbstract read
In one paragraph

Article in Breast cancer (Dove Medical Press), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

11 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. [Metformin suppresses hypoxia-inducible factor-1Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2024
    Article
  8. Article
  9. Article
  10. Review
  11. 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

8 authors at 3 institutions in 2 countries.

Ruibin WangDepartment of Emergency, Beijing Shijitan Hospital, Capital Medical University, Beijing, People's Republic of China.ORCID 0000-0001-9592-1539
Yuchen LiCell and Molecular Biology, Sid Faithfull Brain Cancer Laboratory, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.ORCID 0000-0001-7091-3073
Yanjie ZhaoDepartment of Medical Oncology, Beijing Shijitan Hospital, Capital Medical University, Beijing, People's Republic of China.ORCID 0000-0003-0831-6395
Feng ShiDepartment of Pathology, Beijing Shijitan Hospital, Capital Medical University, Beijing, People's Republic of China.ORCID 0000-0002-1850-7796
Quan ZhouDepartment of Pathology, Cancer Hospital, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing, People's Republic of China.
Jiangping WuDepartment of Cancer Research, Beijing Shijitan Hospital, Capital Medical University, Beijing, People's Republic of China.
Shuzhen LyuDepartment of Breast Surgery, Beijing Shijitan Hospital, Capital Medical University, Beijing, People's Republic of China.
Qingkun SongDepartment of Clinical Epidemiology, Beijing Youan Hospital, Capital Medical University, Beijing, People's Republic of China.ORCID 0000-0002-1159-257X
Capital Medical University · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNQIMR Berghofer Medical Research Institute · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Triple-negative breast cancer (TNBC) is an aggressive subtype of breast cancer. Metformin has been shown to have the potential to inhibit the proliferation of malignant cells. This study aimed to investigate the regulatory effect of metformin on phenotypic tumor-infiltrated lymphocytes (TILs) and mechanisms in TNBC. Methods: Microarray analysis was performed on 4T1 cells post metformin treatment. BALB/c mice were inoculated with 4T1 cells with knockdown/overexpression of C-Jun N-terminal kinase (JNK), and administered with metformin. Phenotypic TILs in the tumor microenvironment (TME) were visualized by immunofluorescence staining. Results: Metformin inhibited 4T1 cell proliferation and increased expression of JNK by 21% in vitro. In vivo, Metformin increased cell counts of CD4 Conclusion: Our study demonstrated that metformin increased the functional phenotype of TILs and associated with JNK pathway, and suppressed the exhausted phenotype of TILs independently to JNK pathway in TNBC microenvironment. Further studies are needed to explore the basic mechanism of action of the drug. Metformin has potentially enhanced efficacy when used in combination with immunotherapy against TNBC.

Indexed as

C-Jun N-terminal kinasemetforminphenotypic tumor-infiltrated lymphocytestriple-negative breast cancer

Identifiers

PMID36482884
PMCPMC9725923
OpenAlexW4311020922

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.