Evidence map›Paper›PMID 14630803›Full record

ArticleBlood2004

Characterization of clonogenic multiple myeloma cells.

William Matsui, Carol Ann Huff, Qiuju Wang, Matthew T Malehorn, James Barber, Yvette Tanhehco, B Douglas Smith, Curt I Civin, Richard J Jones

2 registry-linked trialsOpen access · bronzeAbstract read
In one paragraph

Article in Blood, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 352 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
352citing papers in PubMed, 1 pooled it
7.6field-weighted citation impact, top 2% 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.

NCT01820546 completednot on this mapstarted 2013, after this paper: background citation

Flow Cytometric Definition and Prognostic Effects of Multiple Myeloma Cancer Stem Cells

TypeobservationalSponsorAnkara UniversityRan2013 to 2016Enrolled96ConditionsMultiple Myeloma
NCT03706547 phase1unknown statusnot on this mapstarted 2018, after this paper: background citation

Clinical Study of Anti-CD19/BCMA Bispecific Chimeric Antigen Receptors (CARs) T Cell Therapy for Relapsed and Refractory Multiple Myeloma

TypeinterventionalSponsorPeng LiuRan2018 to 2021Enrolled20ConditionsMultiple Myeloma in Relapse, Multiple Myeloma ProgressionArmsanti-CD19/BCMA CAR-T cells, Fludarabine, Cyclophosphamide
3 · Its place in the literature

Who cites it

352 citing papers in PubMed, 1 synthesis or guideline pooled it, 789 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Article
  6. Article
  7. Review
  8. SSTNSignal transduction and targeted therapy · 2026
    Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. Review
  17. Article
  18. Review
  19. Review
  20. Review

292 more citing papers are in PubMed but not listed here.

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

9 authors at 2 institutions in 1 country.

William MatsuiSidney Kimmel Comprehensive Cancer Center, John Hopkins University School of Medicine, Bunting-Blaustein Cancer Research Bldg, Rm 245, 1650 Orleans St, Baltimore, MD 21231, USA. matsuwi@jhmi.edu
Carol Ann Huff
Qiuju Wang
Matthew T Malehorn
James Barber
Yvette Tanhehco
B Douglas Smith
Curt I Civin
Richard J Jones
Johns Hopkins University · USSidney Kimmel Comprehensive Cancer Center · US

Funding

TUMOR VACCINESP01CA015396 · NCI · JOHNS HOPKINS UNIVERSITY · PI HESS, ALLAN D · 1985 to 2016
$38.1M
THERAPEUTIC USE OF STEM CELLSP01CA070970 · NCI · JOHNS HOPKINS UNIVERSITY · PI CIVIN, CURT I · 1998 to 2012
$23.7M
Cancer Stem Cell Targeting in Multiple MyelomaR01CA127574 · NCI · JOHNS HOPKINS UNIVERSITY · PI MATSUI, WILLIAM H · 2008 to 2012
$1.6M
NCI NIH HHS P01 CA015396NCI NIH HHS P01 CA070970NCI NIH HHS P01CA15396NCI NIH HHS P01CA70970NCI NIH HHS R01 CA127574
6 · The paper itself

Abstract

The identity of the cells responsible for the initiation and maintenance of multiple myeloma (MM) remains unclear largely because of the difficulty growing MM cells in vitro and in vivo. MM cell lines and clinical specimens are characterized by malignant plasma cells that express the cell surface antigen syndecan-1 (CD138); however, CD138 expression is limited to terminally differentiated plasma cells during B-cell development. Moreover, circulating B cells that are clonally related to MM plasma cells have been reported in some patients with MM. We found that human MM cell lines contained small (< 5%) subpopulations that lacked CD138 expression and had greater clonogenic potential in vitro than corresponding CD138+ plasma cells. CD138- cells from clinical MM samples were similarly clonogenic both in vitro and in nonobese diabetic/severe combined immunodeficiency (NOD/SCID) mice, whereas CD138+ cells were not. Furthermore, CD138- cells from both cell lines and clinical samples phenotypically resembled postgerminal center B cells, and their clonogenic growth was inhibited by the anti-CD20 monoclonal antibody rituximab. These data suggest that MM "stem cells" are CD138- B cells with the ability to replicate and subsequently differentiate into malignant CD138+ plasma cells.

Indexed as

AnimalsAntibodies, MonoclonalAntibodies, Monoclonal, Murine-DerivedAntigens, CD20Antigens, CD34Antineoplastic AgentsBiomarkersB-LymphocytesClone CellsHumansImmunophenotypingMembrane GlycoproteinsMiceMice, Inbred NODMice, SCIDMultiple MyelomaAntibodies, MonoclonalAntibodies, Monoclonal, Murine-DerivedAntigens, CD20Antigens, CD34Antineoplastic AgentsBiomarkersMembrane GlycoproteinsProteoglycansRituximabSDC1 protein, humanSdc1 protein, mouseSyndecan-1Syndecans

Identifiers

PMID14630803
PMCPMC3311914
OpenAlexW2045927984

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.