Evidence map›Paper›PMID 23334979›Full record

ArticleThe Prostate2013

Characterization of osteoblastic and osteolytic proteins in prostate cancer bone metastases.

Sandy R Larson, Xiaotun Zhang, Ruth Dumpit, Ilsa Coleman, Bryce Lakely, Martine Roudier, Celestia S Higano, Lawrence D True, Paul H Lange, Bruce Montgomery and 4 more

Abstract read
In one paragraph

Article in The Prostate, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 1 pooled it
3.5field-weighted citation impact, top 7% 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

44 citing papers in PubMed, 1 synthesis or guideline pooled it, 67 citations in OpenAlex.

  1. Pooled it
  2. Review
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  4. Review
  5. Review
  6. Article
  7. Article
  8. Silencing of matrix metalloprotease-12 delays the progression of castration-resistant prostate cancer by regulating autophagy and lipolysis.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2024
    Article
  9. Review
  10. The Emerging Role of MMP12 in the Oral Environment.International journal of molecular sciences · 2023
    Review
  11. Article
  12. StagingEuropean journal of nuclear medicine and molecular imaging · 2022
    Article
  13. Article
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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

14 authors at 2 institutions in 1 country.

Sandy R LarsonDepartment of Urology, University of Washington, Seattle, Washington 98195, USA.
Xiaotun Zhang
Ruth Dumpit
Ilsa Coleman
Bryce Lakely
Martine Roudier
Celestia S Higano
Lawrence D True
Paul H Lange
Bruce Montgomery
Eva Corey
Peter S Nelson
Robert L Vessella
Colm Morrissey
University of Washington · USFred Hutch Cancer Center · US

Funding

TRANSCRIPTOME AND PROTEOME STRATIFICATION OF PROSTATE ADENOCARCINOMA PHENOTYPESP50CA097186 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI John Kyung Lee · 2002 to 2026
$58.1M
Transmembrane Proteases and Prostate CarcinogenesisP01CA085859 · NCI · UNIVERSITY OF WASHINGTON · PI VESSELLA, ROBERT LOUIS · 2002 to 2013
$21.2M
NCI NIH HHS P01 CA085859NCI NIH HHS P01CA085859NCI NIH HHS P50 CA097186NCI NIH HHS P50CA097186NCI NIH HHS P50CA97186
6 · The paper itself

Abstract

backgroundApproximately 90% of patients who die of Prostate Cancer (PCa) have bone metastases, which promote a spectrum of osteoblastic, osteolytic or mixed bone responses. Numerous secreted proteins have been reported to promote osteoblastic or osteolytic bone responses. We determined whether previously identified and/or novel proteins were associated with the osteoblastic or osteolytic response in clinical specimens of PCa bone metastases.

methodsGene expression was analyzed on 14 PCa metastases from 11 patients by microarray profiling and qRT-PCR, and protein expression was analyzed on 33 PCa metastases from 30 patients by immunohistochemistry on highly osteoblastic and highly osteolytic bone specimens.

resultsTranscript and protein levels of BMP-2, BMP-7, DKK-1, ET-1, and Sclerostin were not significantly different between osteoblastic and osteolytic metastases. However, levels of OPG, PGK1, and Substance P proteins were increased in osteoblastic samples. In addition, Emu1, MMP-12, and sFRP-1 were proteins identified with a novel role of being associated with either the osteoblastic or osteolytic bone response.

conclusionsThis is the first detailed analysis of bone remodeling proteins in human specimens of PCa bone metastases. Three proteins not previously shown to be involved may have a role in the PCa bone response. Furthermore, our data suggests that the relative expression of numerous, rather than a single, bone remodeling proteins determine the bone response in PCa bone metastases.

Indexed as

AgedBone Morphogenetic ProteinsBone NeoplasmsBone RemodelingEndothelin-1Gene ExpressionHumansImmunohistochemistryIntercellular Signaling Peptides and ProteinsMaleNeoplasm ProteinsOsteoblastsOsteolysisPhosphoglycerate KinaseProstatic NeoplasmsSubstance PBone Morphogenetic ProteinsDKK1 protein, humanEndothelin-1Intercellular Signaling Peptides and ProteinsNeoplasm ProteinsPGK1 protein, humanPhosphoglycerate KinaseSubstance P

Identifiers

PMID23334979
PMCPMC4214278
OpenAlexW2037248793

What OpenQuestion holds

Textmetadata
LicenceTDM
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.