Evidence map›Paper›PMID 25061178›Full record

ArticleBlood2014

CYR61/CCN1 overexpression in the myeloma microenvironment is associated with superior survival and reduced bone disease.

Sarah K Johnson, James P Stewart, Rakesh Bam, Pingping Qu, Bart Barlogie, Frits van Rhee, John D Shaughnessy, Joshua Epstein, Shmuel Yaccoby

Abstract read
In one paragraph

Article in Blood, 2014. 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
1.7field-weighted citation impact, top 16% 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, 27 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Management of Myeloma Bone Lesions.International journal of molecular sciences · 2021
    Review
  8. Review
  9. CCN1/Cyr61 Is Required in Osteoblasts for Responsiveness to the Anabolic Activity of PTH.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2020
    Article
  10. Article
  11. Article
  12. Article
  13. Protein PEGylation for cancer therapy: bench to bedside.Journal of cell communication and signaling · 2019
    Review
  14. Article
  15. Review
  16. Article
  17. The role of the CCN family of proteins in blood cancers.Journal of cell communication and signaling · 2016
    Article
  18. The role of CCN family genes in haematological malignancies.Journal of cell communication and signaling · 2015
    Article
  19. Matricellular proteins as regulators of cancer metastasis to bone.Matrix biology : journal of the International Society for Matrix Biology
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Sarah K JohnsonMyeloma Institute for Research and Therapy, University of Arkansas for Medical Sciences, Little Rock, AR;
James P StewartMyeloma Institute for Research and Therapy, University of Arkansas for Medical Sciences, Little Rock, AR;
Rakesh BamMyeloma Institute for Research and Therapy, University of Arkansas for Medical Sciences, Little Rock, AR;
Pingping QuCancer Research and Biostatistics, Seattle, WA; and.
Bart BarlogieMyeloma Institute for Research and Therapy, University of Arkansas for Medical Sciences, Little Rock, AR;
Frits van RheeMyeloma Institute for Research and Therapy, University of Arkansas for Medical Sciences, Little Rock, AR;
John D ShaughnessySignal Genetics, LLC, New York, NY.
Joshua EpsteinMyeloma Institute for Research and Therapy, University of Arkansas for Medical Sciences, Little Rock, AR;
Shmuel YaccobyMyeloma Institute for Research and Therapy, University of Arkansas for Medical Sciences, Little Rock, AR;
University of Arkansas for Medical Sciences · USCancer Research And Biostatistics · USSignal Genetics (United States) · US

Funding

Tumor Cell-Microenvironment Interactions in the Molecular Pathogenesis of MultiplP01CA055819 · NCI · UNIV OF ARKANSAS FOR MED SCIS · PI BELLAMY, WILLIAM T · 1993 to 2013
$49.7M
NCI NIH HHS CA55819NCI NIH HHS P01 CA055819
6 · The paper itself

Abstract

Secreted protein CCN1, encoded by CYR61, is involved in wound healing, angiogenesis, and osteoblast differentiation. We identified CCN1 as a microenvironmental factor produced by mesenchymal cells and overexpressed in bones of a subset of patients with monoclonal gammopathy of undetermined significance (MGUS), asymptomatic myeloma (AMM), and multiple myeloma (MM). Our analysis showed that overexpression of CYR61 was independently associated with superior overall survival of MM patients enrolled in our Total Therapy 3 protocol. Moreover, elevated CCN1 was associated with a longer time for MGUS/AMM to progress to overt MM. During remission from MM, high levels of CCN1 were associated with superior progression-free and overall survival and stratified patients with molecularly defined high-risk MM. Recombinant CCN1 directly inhibited in vitro growth of MM cells, and overexpression of CYR61 in MM cells reduced tumor growth and prevented bone destruction in vivo in severe combined immunodeficiency-hu mice. Signaling through αvβ3 was required for CCN1 prevention of bone disease. CYR61 expression may signify early perturbation of the microenvironment before conversion to overt MM and may be a compensatory mechanism to control MM progression. Therapeutics that upregulate CYR61 should be investigated for treating MM bone disease.

Indexed as

Gene ExpressionAnimalsAsymptomatic DiseasesBiopsyBone and BonesBone DiseasesBone MarrowCell Line, TumorCysteine-Rich Protein 61Disease Models, AnimalDisease ProgressionHeterograftsHumansMiceMonoclonal Gammopathy of Undetermined SignificanceMultiple MyelomaCysteine-Rich Protein 61

Identifiers

PMID25061178
PMCPMC4186535
OpenAlexW2005157540

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.