Evidence map›Paper›PMID 25015330›Full record

ArticleOncotarget2014

Multiple myeloma dell-derived microvesicles are enriched in CD147 expression and enhance tumor cell proliferation.

Bonnie K Arendt, Denise K Walters, Xiaosheng Wu, Renee C Tschumper, Diane F Jelinek

Abstract read
In one paragraph

Article in Oncotarget, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
–field-weighted citation impact
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

46 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Soluble CD147 (BSG) as a Prognostic Marker in Multiple Myeloma.Current issues in molecular biology · 2022
    Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Long-chain polyunsaturated omega-3 fatty acids reduce multiple myeloma exosome-mediated suppression of NK cell cytotoxicity.Daru : journal of Faculty of Pharmacy, Tehran University of Medical Sciences · 2020
    Article
  18. Microvesicles in Cancer: Small Size, Large Potential.International journal of molecular sciences · 2020
    Review
  19. Article
  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

5 authors.

Bonnie K ArendtDepartment of Immunology, Division of Hematology, Mayo Clinic, College of Medicine, Rochester, MN.
Denise K WaltersDepartment of Immunology, Division of Hematology, Mayo Clinic, College of Medicine, Rochester, MN.
Xiaosheng WuDepartment of Immunology, Division of Hematology, Mayo Clinic, College of Medicine, Rochester, MN.
Renee C TschumperDepartment of Immunology, Division of Hematology, Mayo Clinic, College of Medicine, Rochester, MN.
Diane F JelinekDepartment of Immunology, Division of Hematology, Mayo Clinic, College of Medicine, Rochester, MN. Department of Medicine, Mayo Clinic, College of Medicine, Rochester, MN.

Funding

Women's Cancer ProgramP30CA015083 · NCI · MAYO CLINIC ROCHESTER · PI Felicity Enders · 1985 to 2026
$151.3M
Metabolic Reprogramming: Essential Role and Early Marker of MGUS ProgressionR21CA164204 · NCI · MAYO CLINIC ROCHESTER · PI JELINEK, DIANE F · 2012 to 2013
$368k
CD147 Biological Function and Role as a Biomarker of MGUS to Myeloma ProgressionR21CA164232 · NCI · MAYO CLINIC ROCHESTER · PI JELINEK, DIANE F · 2012 to 2013
$365k
NCI NIH HHS CA164204NCI NIH HHS CA164232NCI NIH HHS P30 CA015083NCI NIH HHS R21 CA164204NCI NIH HHS R21 CA164232
6 · The paper itself

Abstract

Multiple myeloma (MM) is characterized by the clonal expansion of malignant plasma cells within the bone marrow. There is a growing literature that tumor cells release biologically active microvesicles (MVs) that modify both local and distant microenvironments. In this study, our goals were to determine if MM cells release MVs, and if so, begin to characterize their biologic activity. Herein we present clear evidence that not only do both patient MM cells and human MM cell lines (HMCLs) release MVs, but that these MVs stimulate MM cell growth. Of interest, MM-derived MVs were enriched with the biologically active form of CD147, a transmembrane molecule previously shown by us to be crucial for MM cell proliferation. Using MVs isolated from HMCLs stably transfected with a CD147-GFP fusion construct (CD147GFP), we observed binding and internalization of MV-derived CD147 with HMCLs. Cells with greater CD147GFP internalization proliferated at a higher rate than did cells with less CD147GFP association. Lastly, MVs obtained from CD147 downregulated HMCLs were attenuated in their ability to stimulate HMCL proliferation. In summary, this study demonstrates the significance of MV shedding and MV-mediated intercellular communication on malignant plasma cell proliferation, and identifies the role of MV-enriched CD147 in this process.

Indexed as

BasiginCell Line, TumorCell MembraneCell ProliferationHumansImmunophenotypingMultiple MyelomaBasigin

Identifiers

PMID25015330
PMCPMC4170605

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Registered trials

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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.