Evidence map›Paper›PMID 37699574›Full record

ArticleBritish journal of haematology2023

Myeloperoxidase creates a permissive microenvironmental niche for the progression of multiple myeloma.

Connor M D Williams, Jacqueline E Noll, Alanah L Bradey, Jvaughn Duggan, Vicki J Wilczek, Makutiro G Masavuli, Branka Grubor-Bauk, Romana A Panagopoulos, Duncan R Hewett, Krzysztof M Mrozik and 3 more

Open access · hybridAbstract read
In one paragraph

Article in British journal of haematology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

7 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
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  5. MDSC: a new potential breakthrough in CAR-T therapy for solid tumors.Cell communication and signaling : CCS · 2024
    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 2 institutions in 1 country.

Connor M D WilliamsMyeloma Research Laboratory, Faculty of Health and Medical Sciences, School of Biomedicine, University of Adelaide, Adelaide, Australia.
Jacqueline E NollMyeloma Research Laboratory, Faculty of Health and Medical Sciences, School of Biomedicine, University of Adelaide, Adelaide, Australia.
Alanah L BradeyMyeloma Research Laboratory, Faculty of Health and Medical Sciences, School of Biomedicine, University of Adelaide, Adelaide, Australia.
Jvaughn DugganMyeloma Research Laboratory, Faculty of Health and Medical Sciences, School of Biomedicine, University of Adelaide, Adelaide, Australia.
Vicki J WilczekMyeloma Research Laboratory, Faculty of Health and Medical Sciences, School of Biomedicine, University of Adelaide, Adelaide, Australia.
Makutiro G MasavuliViral Immunology Group, Discipline of Surgery, Basil Hetzel Institute for Translational Health Research, University of Adelaide, Adelaide, Australia.
Branka Grubor-BaukViral Immunology Group, Discipline of Surgery, Basil Hetzel Institute for Translational Health Research, University of Adelaide, Adelaide, Australia.
Romana A PanagopoulosSolid Tumour Program, Precision Cancer Medicine Theme, South Australian Health and Medical Research Institute, Adelaide, Australia.
Duncan R HewettMyeloma Research Laboratory, Faculty of Health and Medical Sciences, School of Biomedicine, University of Adelaide, Adelaide, Australia.
Krzysztof M MrozikMyeloma Research Laboratory, Faculty of Health and Medical Sciences, School of Biomedicine, University of Adelaide, Adelaide, Australia.
Andrew C W ZannettinoMyeloma Research Laboratory, Faculty of Health and Medical Sciences, School of Biomedicine, University of Adelaide, Adelaide, Australia.ORCID 0000-0002-6646-6167
Kate VandykeMyeloma Research Laboratory, Faculty of Health and Medical Sciences, School of Biomedicine, University of Adelaide, Adelaide, Australia.ORCID 0000-0002-1033-849X
Vasilios PanagopoulosMyeloma Research Laboratory, Faculty of Health and Medical Sciences, School of Biomedicine, University of Adelaide, Adelaide, Australia.ORCID 0000-0002-6879-1262
South Australian Health and Medical Research Institute · AUBasil Hetzel Institute · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Expression of myeloperoxidase (MPO), a key inflammatory enzyme restricted to myeloid cells, is negatively associated with the development of solid tumours. Activated myeloid cell populations are increased in multiple myeloma (MM); however, the functional consequences of myeloid-derived MPO within the myeloma microenvironment are unknown. Here, the role of MPO in MM pathogenesis was investigated, and the capacity for pharmacological inhibition of MPO to impede MM progression was evaluated. In the 5TGM1-KaLwRij mouse model of myeloma, the early stages of tumour development were associated with an increase in CD11b

Indexed as

Multiple MyelomaPeroxidaseTumor MicroenvironmentAnimalsBone MarrowDisease Models, AnimalMiceMyeloid CellsPeroxidaseimmune suppressionmultiple myelomamyeloid-derived suppressor cellsmyeloperoxidase

Identifiers

PMID37699574
PMCPMC10952523
OpenAlexW4386630143

What Socratic 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 Socratic graph.