Evidence map›Paper›PMID 38501542›Full record

ArticleImmunity, inflammation and disease2024

Obesity correlates with the immunosuppressive ILC2s-MDSCs axis in advanced breast cancer.

Wei Liu, Bingyu Li, Dan Liu, Bing Zhao, Gang Sun, Jianbing Ding

Open access · goldAbstract read
In one paragraph

Article in Immunity, inflammation and disease, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Review
  3. Mechanisms by which obesity regulates inflammation and anti-tumor immunity in cancer.Biochemical and biophysical research communications · 2024
    Review
  4. 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

6 authors at 1 institution in 1 country.

Wei LiuSchool of Public Health, Xinjiang Medical University, Urumqi, People's Republic of China.
Bingyu LiDepartment of Mammary Medicine, Affiliated Tumor Hospital of Xinjiang Medical University, Urumqi, People's Republic of China.
Dan LiuDepartment of Mammary Medicine, Affiliated Tumor Hospital of Xinjiang Medical University, Urumqi, People's Republic of China.
Bing ZhaoDepartment of Mammary Medicine, Affiliated Tumor Hospital of Xinjiang Medical University, Urumqi, People's Republic of China.
Gang SunXinjiang Uygur Autonomous Region Cancer Center/Xinjiang Key Laboratory of Oncology, Urumqi, People's Republic of China.
Jianbing DingXinjiang Key Laboratory of Molecular Biology for Endemic Diseases, Urumqi, Xinjiang, People's Republic of China.ORCID 0000-0001-5506-7665
Xinjiang Medical University · CN

Funding

Key Laboratory of Oncology of Xinjiang Uyghur Autonomous Region, the Affiliated Tumor Hospital of Xinjiang Medical UniversityRegional Project of the Natural Science Foundation of China 82060520
6 · The paper itself

Abstract

aimWe investigated the relationship between the group 2 innate lymphoid cells (ILC2s)-myeloid-derived suppressor cells (MDSCs) axis and obesity-related breast cancer.

methodsFifty-eight patients with breast cancer who had first relapse and metastasis between January 2019 and August 2021 were enrolled. The proportions of ILC2s and MDSCs in blood and the levels of cytokines in serum were detected with flow cytometry. Correlation analysis among clinical characteristics (such as body mass index [BMI]), cytokines, ILC2s, and MDSCs was conducted.

resultsThere was a significant difference in the proportions of ILC2s and MDSCs between the high BMI group and the normal BMI group (p < .05). In the triple-negative breast cancer (TNBC) patients, the proportions of ILC2s and MDSCs in the obese group were significantly higher than those in the nonobese group (p < .05). In all breast cancer patients, there was a positive correlation between BMI and the ILC2s-MDSCs axis (p < .05). However, there was no correlation observed between the number of metastases, progression-free survival, and the ILC2s-MDSCs axis (p > .05). Additionally, ILC2s showed positive correlations with MDSCs, interleukin-5 (IL-5), IL-10, IL-17A, (PD-L1), programmed cell death 2 ligand 2 (PD-L2), and molecular typing (p < .05). Similarly, MDSCs exhibited positive correlations with IL-5, IL-8, IL-9, IL-17A, PD-L1, and PD-L2 (p < .05). In patients with TNBC, there was a positive correlation between BMI and IL-5 (p < .05).

conclusionConclusively, obesity may enhance the immunosuppressive effect of the ILC2-MDSC axis in advanced breast cancer. IL-5 may play a vital role in the ILC2-MDSC axis and obesity in TNBC.

Indexed as

Myeloid-Derived Suppressor CellsTriple Negative Breast NeoplasmsB7-H1 AntigenCytokinesHumansImmunity, InnateInterleukin-17Interleukin-5LymphocytesB7-H1 AntigenCytokinesInterleukin-17Interleukin-5advanced breast cancergroup 2 innate lymphoid cellsinflammatory factorsinterleukinmyeloid-derived suppressor cellsobesity

Identifiers

PMID38501542
PMCPMC10949396
OpenAlexW4392956366

What OpenQuestion holds

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LicenceCC BY
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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.