Evidence map›Paper›PMID 22829171›Full record

ArticleBlood cancer journal2011

Myeloma cells suppress osteoblasts through sclerostin secretion.

S Colucci, G Brunetti, A Oranger, G Mori, F Sardone, G Specchia, E Rinaldi, P Curci, V Liso, G Passeri and 3 more

Abstract read
In one paragraph

Article in Blood cancer journal, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers.

0numbers the graph read from it
0cells of the map it votes in
72citing 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

72 citing papers in PubMed.

  1. Review
  2. Article
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  6. Article
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  9. Article
  10. Trabecular bone remodeling in the aging mouse: A micro-multiphysics agent-basedFrontiers in bioengineering and biotechnology · 2023
    Article
  11. Article
  12. Review
  13. Pathophysiology and therapeutic advances in myeloma bone disease.Chronic diseases and translational medicine · 2022
    Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Positive and Negative Regulators of Sclerostin Expression.International journal of molecular sciences · 2022
    Review
  19. Pathogenesis and Treatment of Myeloma-Related Bone Disease.International journal of molecular sciences · 2022
    Review
  20. Pathogenesis and treatment of multiple myeloma bone disease.The Japanese dental science review · 2021
    Review

12 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

13 authors.

S Colucci
G Brunetti
A Oranger
G Mori
F Sardone
G Specchia
E Rinaldi
P Curci
V Liso
G Passeri
A Zallone
R Rizzi
M Grano

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Wingless-type (Wnt) signaling through the secretion of Wnt inhibitors Dickkopf1, soluble frizzled-related protein-2 and -3 has a key role in the decreased osteoblast (OB) activity associated with multiple myeloma (MM) bone disease. We provide evidence that another Wnt antagonist, sclerostin, an osteocyte-expressed negative regulator of bone formation, is expressed by myeloma cells, that is, human myeloma cell lines (HMCLs) and plasma cells (CD138+ cells) obtained from the bone marrow (BM) of a large number of MM patients with bone disease. We demonstrated that BM stromal cells (BMSCs), differentiated into OBs and co-cultured with HMCLs showed, compared with BMSCs alone, reduced expression of major osteoblastic-specific proteins, decreased mineralized nodule formation and attenuated the expression of members of the activator protein 1 transcription factor family (Fra-1, Fra-2 and Jun-D). Moreover, in the same co-culture system, the addition of neutralizing anti-sclerostin antibodies restored OB functions by inducing nuclear accumulation of β-catenin. We further demonstrated that the upregulation of receptor activator of nuclear factor κ-B ligand and the downregulation of osteoprotegerin in OBs were also sclerostin mediated. Our data indicated that sclerostin secretion by myeloma cells contribute to the suppression of bone formation in the osteolytic bone disease associated to MM.

Identifiers

PMID22829171
PMCPMC3255263

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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.