Evidence map›Paper›PMID 23023717›Full record

ReviewThe Journal of clinical investigation2012

Molecular pathogenesis of multiple myeloma and its premalignant precursor.

W Michael Kuehl, P Leif Bergsagel

Open access · bronzeAbstract readReview
In one paragraph

Review in The Journal of clinical investigation, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 193 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
193citing papers in PubMed, 3 pooled it
19.9field-weighted citation impact, top 1% 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

193 citing papers in PubMed, 3 syntheses or guidelines pooled it, 333 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Guideline
  4. GP130 activation induces myeloma and collaborates with MYC.The Journal of clinical investigation · 2014
    Trial
  5. Trial
  6. Article
  7. Article
  8. Article
  9. Nanomedicine-Based Strategies for Multiple Myeloma Therapy.International journal of nanomedicine · 2026
    Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Next-Generation Therapies for Multiple Myeloma.Annual review of cancer biology · 2024
    Article
  18. Immunocompetent Mouse Models of Multiple Myeloma: Therapeutic Implications.Hematology/oncology clinics of North America · 2024
    Review
  19. Lifestyle Factors and Cancer: A Narrative Review.Mayo Clinic proceedings. Innovations, quality & outcomes · 2024
    Article
  20. Article

133 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

2 authors at 2 institutions in 1 country.

W Michael KuehlGenetics Branch, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland, USA.
P Leif Bergsagel
National Cancer Institute · USPalmetto Hematology Oncology · US

Funding

Trageting the Multiple Myeloma EpigenomeP50CA100707 · NCI · DANA-FARBER CANCER INSTITUTE · PI ANDERSON, KENNETH C., MUNSHI, NIKHIL C. · 2003 to 2023
$45.0M
Molecular Pathogenesis of Multiple MyelomaZIASC006581 · NCI · DIVISION OF CLINICAL SCIENCES - NCI · PI KUEHL, WALTER · 2009 to 2015
$4.5M
Genomic Rearrangements in Multiple MyelomaZIABC010910 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI KUEHL, WALTER · 2009 to 2015
$3.8M
Mouse models of age-associated monoclonal gammopathyR01AG020686 · NIA · WEILL MEDICAL COLLEGE OF CORNELL UNIV · PI BERGSAGEL, PETER LEIF · 2003 to 2014
$3.3M
Comparative Pharmaco-oncogenomics of Myeloma Drug ResistanceR01CA136671 · NCI · MAYO CLINIC ARIZONA · PI BERGSAGEL, PETER LEIF · 2009 to 2013
$1.6M
Molecular Pathogenesis of Multiple MyelomaR01CA133966 · NCI · MAYO CLINIC ARIZONA · PI BERGSAGEL, PETER LEIF · 2009 to 2013
$1.6M
Mouse Models of Age-Associated Monoclonal GammopathyR56AG020686 · NIA · MAYO CLINIC ARIZONA · PI BERGSAGEL, PETER LEIF · 2009 to 2009
$405k
NCI NIH HHS CA100707NCI NIH HHS CA133966NCI NIH HHS CA136671NCI NIH HHS P50 CA100707NCI NIH HHS R01 CA133966NCI NIH HHS R01 CA136671NIA NIH HHS AG020686NIA NIH HHS R01 AG020686NIA NIH HHS R56 AG020686
6 · The paper itself

Abstract

Multiple myeloma is a monoclonal tumor of plasma cells, and its development is preceded by a premalignant tumor with which it shares genetic abnormalities, including universal dysregulation of the cyclin D/retinoblastoma (cyclin D/RB) pathway. A complex interaction with the BM microenvironment, characterized by activation of osteoclasts and suppression of osteoblasts, leads to lytic bone disease. Intratumor genetic heterogeneity, which occurs in addition to intertumor heterogeneity, contributes to the rapid emergence of drug resistance in high-risk disease. Despite recent therapeutic advances, which have doubled the median survival time, myeloma continues to be a mostly incurable disease. Here we review the current understanding of myeloma pathogenesis and insight into new therapeutic strategies provided by animal models and genetic screens.

Indexed as

Bone RemodelingCell Transformation, NeoplasticCyclin D1Disease ProgressionDrug Resistance, NeoplasmGenes, bcl-1Genes, RetinoblastomaHumansImmunoglobulin Heavy ChainsImmunophenotypingModels, BiologicalMonoclonal Gammopathy of Undetermined SignificanceMultiple MyelomaNeoplasm ProteinsNeoplastic Stem CellsOncogene Proteins, FusionCCND1 protein, humanCyclin D1Immunoglobulin Heavy ChainsNeoplasm ProteinsOncogene Proteins, FusionRetinoblastoma Protein

Identifiers

PMID23023717
PMCPMC3461901
OpenAlexW2056172893

What OpenQuestion holds

Textmetadata
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.