Evidence map›Paper›PMID 31881770›Full record

ArticleInternational journal of molecular sciences2019

Single Cell Mass Cytometry Revealed the Immunomodulatory Effect of Cisplatin Via Downregulation of Splenic CD44+, IL-17A+ MDSCs and Promotion of Circulating IFN-γ+ Myeloid Cells in the 4T1 Metastatic Breast Cancer Model.

József Á Balog, László Hackler, Anita K Kovács, Patrícia Neuperger, Róbert Alföldi, Lajos I Nagy, László G Puskás, Gábor J Szebeni

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

30 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Application of mass cytometry in the immune microenvironment of breast cancer.Medical oncology (Northwood, London, England) · 2025
    Review
  6. Article
  7. Article
  8. Article
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  10. Polysaccharide isolated fromInternational journal of biological sciences · 2024
    Article
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  16. AnHeliyon · 2022
    Article
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  18. Review
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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 2 institutions in 1 country.

József Á BalogLaboratory of Functional Genomics, Biological Research Centre, Temesvári krt. 62, H6726 Szeged, Hungary.
László HacklerAstridBio Technologies Ltd., Also kikötő sor 11/D, H6726 Szeged, Hungary.
Anita K KovácsAvidin Ltd., Also kikötő sor 11/D, H6726 Szeged, Hungary.
Patrícia NeupergerLaboratory of Functional Genomics, Biological Research Centre, Temesvári krt. 62, H6726 Szeged, Hungary.
Róbert AlföldiPhD School in Biology, University of Szeged, H6726 Szeged, Hungary.
Lajos I NagyAvidin Ltd., Also kikötő sor 11/D, H6726 Szeged, Hungary.
László G PuskásLaboratory of Functional Genomics, Biological Research Centre, Temesvári krt. 62, H6726 Szeged, Hungary.
Gábor J SzebeniLaboratory of Functional Genomics, Biological Research Centre, Temesvári krt. 62, H6726 Szeged, Hungary.
University of Szeged · HUHUN-REN Szegedi Biológiai Kutatóközpont · HU

Funding

EUREKA Network Program H2020 E12655 MITOMEJános Bolyai Research Scholarship of the Hungarian Academy of Sciences BO/00139/17/8National Research, Development and Innovation Office GINOP-2.3.2-15-2016-00001New National Excellence Program of the Ministry for Innovation and Technology UNKP-19-4-SZTE-3
6 · The paper itself

Abstract

The treatment of metastatic breast cancer remained a challenge despite the recent breakthrough in the immunotherapy regimens. Here, we addressed the multidimensional immunophenotyping of 4T1 metastatic breast cancer by the state-of-the-art single cell mass cytometry (CyTOF). We determined the dose and time dependent cytotoxicity of cisplatin on 4T1 cells by the xCelligence real-time electronic sensing assay. Cisplatin treatment reduced tumor growth, number of lung metastasis, and the splenomegaly of 4T1 tumor bearing mice. We showed that cisplatin inhibited the tumor stroma formation, the polarization of carcinoma-associated fibroblasts by the diminished proteolytic activity of fibroblast activating protein. The CyTOF analysis revealed the emergence of CD11b+/Gr-1+/CD44+ or CD11b+/Gr-1+/IL-17A+ myeloid-derived suppressor cells (MDSCs) and the absence of B220+ or CD62L+ B-cells, the CD62L+/CD4+ and CD62L+/CD8+ T-cells in the spleen of advanced cancer. We could show the immunomodulatory effect of cisplatin via the suppression of splenic MDSCs and via the promotion of peripheral IFN-γ+ myeloid cells. Our data could support the use of low dose chemotherapy with cisplatin as an immunomodulatory agent for metastatic triple negative breast cancer.

Indexed as

AnimalsBreast NeoplasmsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell Line, TumorCell SurvivalCisplatinDown-RegulationEndopeptidasesFemaleFibroblast Activation Protein AlphaGelatinasesHumansHyaluronan ReceptorsImmunophenotypingInterferon-gammaCD44 protein, humanCisplatinEndopeptidasesFibroblast Activation Protein AlphaGelatinasesHyaluronan ReceptorsInterferon-gammaInterleukin-17Membrane ProteinsSerine Endopeptidasesimmunophenotypingmetastatic breast cancermyeloid-derived suppressor cellssingle cell mass cytometry

Identifiers

PMID31881770
PMCPMC6982301
OpenAlexW2998699399

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.