Evidence map›Paper›PMID 28915615›Full record

ArticleOncotarget2017

Expression of CD38 in myeloma bone niche: A rational basis for the use of anti-CD38 immunotherapy to inhibit osteoclast formation.

Federica Costa, Denise Toscani, Antonella Chillemi, Valeria Quarona, Marina Bolzoni, Valentina Marchica, Rosanna Vescovini, Cristina Mancini, Eugenia Martella, Nicoletta Campanini and 7 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
6.7field-weighted citation impact, top 3% 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

42 citing papers in PubMed, 67 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. CD38 as theranostic target in oncology.Journal of translational medicine · 2024
    Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Review
  20. 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

17 authors at 3 institutions in 1 country.

Federica Costa *Department of Medicine and Surgery, University of Parma, Parma, Italy.
Denise Toscani *Department of Medicine and Surgery, University of Parma, Parma, Italy.
Antonella ChillemiLaboratory of Immunogenetics, Department of Medical Sciences and CeRMS, University of Torino, Torino, Italy.
Valeria QuaronaLaboratory of Immunogenetics, Department of Medical Sciences and CeRMS, University of Torino, Torino, Italy.
Marina BolzoniDepartment of Medicine and Surgery, University of Parma, Parma, Italy.
Valentina MarchicaDepartment of Medicine and Surgery, University of Parma, Parma, Italy.
Rosanna VescoviniClinical Medicine Unit, Department of Medicine and Surgery, University of Parma, Parma, Italy.
Cristina ManciniPathology, "Azienda Ospedaliero-Universitaria di Parma", Parma, Italy.
Eugenia MartellaPathology, "Azienda Ospedaliero-Universitaria di Parma", Parma, Italy.
Nicoletta CampaniniPathology, "Azienda Ospedaliero-Universitaria di Parma", Parma, Italy.
Chiara SchifanoHematology and BMT Center, "Azienda Ospedaliero-Universitaria di Parma", Parma, Italy.
Sabrina BonominiHematology and BMT Center, "Azienda Ospedaliero-Universitaria di Parma", Parma, Italy.
Fabrizio AccardiDepartment of Medicine and Surgery, University of Parma, Parma, Italy.
Alberto L HorensteinLaboratory of Immunogenetics, Department of Medical Sciences and CeRMS, University of Torino, Torino, Italy.
Franco AversaDepartment of Medicine and Surgery, University of Parma, Parma, Italy.
Fabio MalavasiLaboratory of Immunogenetics, Department of Medical Sciences and CeRMS, University of Torino, Torino, Italy.
Nicola GiulianiDepartment of Medicine and Surgery, University of Parma, Parma, Italy.
Ospedale di Parma · ITUniversity of Parma · ITUniversity of Turin · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is known that multiple myeloma (MM) cells express CD38 and that a recently developed human anti-CD38 monoclonal antibody Daratumumab mediates myeloma killing. However, the expression of CD38 and other functionally related ectoenzymes within the MM bone niche and the potential effects of Daratumumab on bone cells are still unknown. This study firstly defines by flow cytometry and immunohistochemistry the expression of CD38 by bone marrow cells in a cohort of patients with MM and indolent monoclonal gammopathies. Results indicate that only plasma cells expressed CD38 at high level within the bone niche. In addition, the flow cytometry analysis shows that CD38 was also expressed by monocytes and early osteoclast progenitors but not by osteoblasts and mature osteoclasts. Indeed, CD38 was lost during

Indexed as

bone diseaseCD38immunotherapymultiple myelomaosteoclast

Identifiers

PMID28915615
PMCPMC5593586
OpenAlexW2614932266

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.