Evidence map›Paper›PMID 31281314›Full record

ArticleFrontiers in immunology2019

SPARC Is a New Myeloid-Derived Suppressor Cell Marker Licensing Suppressive Activities.

Sabina Sangaletti, Giovanna Talarico, Claudia Chiodoni, Barbara Cappetti, Laura Botti, Paola Portararo, Alessandro Gulino, Francesca Maria Consonni, Antonio Sica, Giovanni Randon and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

39 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
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  5. Article
  6. Review
  7. MDSC: a new potential breakthrough in CAR-T therapy for solid tumors.Cell communication and signaling : CCS · 2024
    Review
  8. Article
  9. Emergency myelopoiesis in solid cancers.British journal of haematology · 2024
    Review
  10. Factors Determining Epithelial-Mesenchymal Transition in Cancer Progression.International journal of molecular sciences · 2024
    Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. 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

13 authors at 4 institutions in 1 country.

Sabina SangalettiMolecular Immunology Unit, Department of Research, Fondazione IRCCS Istituto Nazionale dei Tumori di Milano, Milan, Italy.
Giovanna TalaricoMolecular Immunology Unit, Department of Research, Fondazione IRCCS Istituto Nazionale dei Tumori di Milano, Milan, Italy.
Claudia ChiodoniMolecular Immunology Unit, Department of Research, Fondazione IRCCS Istituto Nazionale dei Tumori di Milano, Milan, Italy.
Barbara CappettiMolecular Immunology Unit, Department of Research, Fondazione IRCCS Istituto Nazionale dei Tumori di Milano, Milan, Italy.
Laura BottiMolecular Immunology Unit, Department of Research, Fondazione IRCCS Istituto Nazionale dei Tumori di Milano, Milan, Italy.
Paola PortararoMolecular Immunology Unit, Department of Research, Fondazione IRCCS Istituto Nazionale dei Tumori di Milano, Milan, Italy.
Alessandro GulinoTumor Immunology Unit, University of Palermo, Palermo, Italy.
Francesca Maria ConsonniDepartment of Inflammation and Immunology, Humanitas Clinical and Research Center, Milan, Italy.
Antonio SicaDepartment of Inflammation and Immunology, Humanitas Clinical and Research Center, Milan, Italy.
Giovanni RandonMedical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori di Milano, Milan, Italy.
Massimo Di NicolaMedical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori di Milano, Milan, Italy.
Claudio TripodoTumor Immunology Unit, University of Palermo, Palermo, Italy.
Mario P ColomboMolecular Immunology Unit, Department of Research, Fondazione IRCCS Istituto Nazionale dei Tumori di Milano, Milan, Italy.
Fondazione IRCCS Istituto Nazionale dei Tumori · ITUniversity of Palermo · ITHumanitas University · ITUniversità degli Studi del Piemonte Orientale “Amedeo Avogadro” · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myeloid-derived suppressor cells (MDSC) are well-known key negative regulators of the immune response during tumor growth, however scattered is the knowledge of their capacity to influence and adapt to the different tumor microenvironments and of the markers that identify those capacities. Here we show that the secreted protein acidic and rich in cysteine (SPARC) identifies in both human and mouse MDSC with immune suppressive capacity and pro-tumoral activities including the induction of epithelial-to-mesenchymal transition (EMT) and angiogenesis. In mice the genetic deletion of SPARC reduced MDSC immune suppression and reverted EMT.

Indexed as

AnimalsArginaseBiomarkersEpithelial-Mesenchymal TransitionExtracellular TrapsHumansMiceMice, Inbred BALB CMice, KnockoutMyeloid-Derived Suppressor CellsNF-kappa B p50 SubunitNitric Oxide Synthase Type IIOsteonectinSTAT3 Transcription FactorArg1 protein, mouseArginaseBiomarkersNF-kappa B p50 SubunitNfkb1 protein, mouseNitric Oxide Synthase Type IINos2 protein, mouseOsteonectinSPARC protein, mouseStat3 protein, mouseSTAT3 Transcription Factorbreast cancermyeloid-derived suppressor cellsneutrophilneutrophil extracellular trapsSPARC

Identifiers

PMID31281314
PMCPMC6596449
OpenAlexW2950397474

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.