Evidence map›Paper›PMID 29769142›Full record

ArticleJournal of hematology & oncology2018

Myeloma-derived macrophage inhibitory factor regulates bone marrow stromal cell-derived IL-6 via c-MYC.

Rachel E Piddock, Christopher R Marlein, Amina Abdul-Aziz, Manar S Shafat, Martin J Auger, Kristian M Bowles, Stuart A Rushworth

Open access · goldAbstract readLetter
In one paragraph

Article in Journal of hematology & oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

19 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
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  8. Article
  9. Lessons in aging from Myc knockout mouse models.Frontiers in cell and developmental biology · 2023
    Review
  10. Review
  11. A 3D-Bioprinted Multiple Myeloma Model.Advanced healthcare materials · 2022
    Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Pathogenic Mechanisms of Myeloma Bone Disease and Possible Roles for NRF2.International journal of molecular sciences · 2020
    Review
  18. Review
  19. Review
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

7 authors at 3 institutions in 1 country.

Rachel E PiddockDepartment of Molecular Haematology, Norwich Medical School, The University of East Anglia, Norwich Research Park, Norwich, NR4 7TJ, UK.
Christopher R MarleinDepartment of Molecular Haematology, Norwich Medical School, The University of East Anglia, Norwich Research Park, Norwich, NR4 7TJ, UK.
Amina Abdul-AzizDepartment of Molecular Haematology, Norwich Medical School, The University of East Anglia, Norwich Research Park, Norwich, NR4 7TJ, UK.
Manar S ShafatDepartment of Molecular Haematology, Norwich Medical School, The University of East Anglia, Norwich Research Park, Norwich, NR4 7TJ, UK.
Martin J AugerDepartment of Haematology, Norfolk and Norwich University Hospitals NHS Trust, Colney Lane, Norwich, NR4 7UY, UK.
Kristian M BowlesDepartment of Molecular Haematology, Norwich Medical School, The University of East Anglia, Norwich Research Park, Norwich, NR4 7TJ, UK. kristian.bowles@nnuh.nhs.uk.
Stuart A RushworthDepartment of Molecular Haematology, Norwich Medical School, The University of East Anglia, Norwich Research Park, Norwich, NR4 7TJ, UK. s.rushworth@uea.ac.uk.
Norwich Research Park · GBUniversity of East Anglia · GBNorfolk and Norwich University Hospitals NHS Foundation Trust · GB

Funding

Biotechnology and Biological Sciences Research Council
6 · The paper itself

Abstract

Multiple myeloma (MM) remains an incurable malignancy despite the recent advancements in its treatment. The protective effects of the niche in which it develops has been well documented; however, little has been done to investigate the MM cell's ability to 're-program' cells within its environment to benefit disease progression. Here, we show that MM-derived macrophage migratory inhibitory factor (MIF) stimulates bone marrow stromal cells to produce the disease critical cytokines IL-6 and IL-8, prior to any cell-cell contact. Furthermore, we provide evidence that this IL-6/8 production is mediated by the transcription factor cMYC. Pharmacological inhibition of cMYC in vivo using JQ1 led to significantly decreased levels of serum IL-6-a highly positive prognostic marker in MM patients.

conclusionsOur presented findings show that MM-derived MIF causes BMSC secretion of IL-6 and IL-8 via BMSC cMYC. Furthermore, we show that the cMYC inhibitor JQ1 can reduce BMSC secreted IL-6 in vivo, irrespective of tumor burden. These data provide evidence for the clinical evaluation of both MIF and cMYC inhibitors in the treatment of MM.

Indexed as

Bone Marrow CellsHumansInterleukin-6Interleukin-8Intramolecular OxidoreductasesMacrophage Migration-Inhibitory FactorsMultiple MyelomaProto-Oncogene Proteins c-mycStromal CellsCXCL8 protein, humanIL6 protein, humanInterleukin-6Interleukin-8Intramolecular OxidoreductasesMacrophage Migration-Inhibitory FactorsMIF protein, humanMYC protein, humanProto-Oncogene Proteins c-mycBMSCBone marrowcMYCIL-6IL-8MIFMyelomaStromal

Identifiers

PMID29769142
PMCPMC5956761
OpenAlexW2803644392

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.