Evidence map›Paper›PMID 19671866›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2009

Small integrin-binding proteins as serum markers for prostate cancer detection.

Alka Jain, Dianalee A McKnight, Larry W Fisher, Elizabeth B Humphreys, Leslie A Mangold, Alan W Partin, Neal S Fedarko

Open access · bronzeAbstract readValidation Study
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.9field-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

20 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Cancer Secretome May Influence BSP and DSP Expression in Human Salivary Gland Cells.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2017
    Article
  10. Article
  11. Stability and degradation of fibroblast growth factor 23 (FGF23): the effect of time and temperature and assay type.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2016
    Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. 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

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

7 authors at 2 institutions in 1 country.

Alka JainDivision of Geriatric Medicine & Gerontology, Department of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.
Dianalee A McKnight
Larry W Fisher
Elizabeth B Humphreys
Leslie A Mangold
Alan W Partin
Neal S Fedarko
Johns Hopkins University · USNational Institute of Dental and Craniofacial Research · US

Funding

Bone And Tooth Matrix Biochemistry And MetabolismZIADE000074 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI FISHER, LARRY W · 2009 to 2018
$8.0M
Development/Clinical Validation Markers for Prostate CaU01CA086323 · NCI · JOHNS HOPKINS UNIVERSITY · PI PARTIN, ALAN W · 2000 to 2010
$6.1M
Small integrin-binding proteins and tumor progressionR01CA113865 · NCI · JOHNS HOPKINS UNIVERSITY · PI FEDARKO, NEAL S · 2006 to 2008
$750k
Intramural NIH HHSNCI NIH HHS 2U01 CA86323NCI NIH HHS CA 113865NCI NIH HHS R01 CA113865NCI NIH HHS U01 CA086323
6 · The paper itself

Abstract

purposeThe small integrin-binding ligand N-linked glycoprotein (SIBLING) gene family includes bone sialoprotein (BSP), dentin matrix protein 1 (DMP1), dentin sialophosphoprotein (DSPP), matrix extracellular phosphoglycoprotein (MEPE), and osteopontin (OPN). Previous studies have separately reported elevated expression of BSP, OPN, or DSPP in prostate tumor paraffin sections. We hypothesized that SIBLINGs may be informative serum markers for subjects with prostate cancer.

methodsExpression levels of SIBLINGs in biopsies of normal tissue and tumors from prostate were determined by cDNA array and by immunohistochemical staining with monoclonal antibodies. Competitive ELISAs for measuring total BSP, DSPP, MEPE, and OPN were applied to a test group of 102 subjects with prostate cancer and 110 normal subjects and a validation group of 90 subjects.

resultsBSP, DMP1, DSPP, and OPN exhibited elevated mRNA expression and protein levels in biopsies. BSP, DSPP, and OPN were elevated in serum from prostate cancer subjects, with serum DSPP exhibiting the greatest difference, yielding an area under the receiver operator characteristic curve value of 0.98. Serum BSP and OPN levels were significantly elevated only in late stages, whereas DSPP was significantly elevated at all stages. Optimal serum value cutoff points derived for BSP, OPN, and DSPP were applied as a validation test to a new group of 90 subjects and DSPP yielded a sensitivity of 90% and a specificity of 100%.

conclusionOf the SIBLING gene family members, DSPP appears to be a strong candidate for use in serum assays for prostate cancer detection.

Indexed as

BiomarkersBlood ProteinsCarcinomaGene Expression ProfilingGene Expression Regulation, NeoplasticGlycoproteinsHumansIntegrinsMaleOligonucleotide Array Sequence AnalysisProstatic NeoplasmsProtein BindingRNA, MessengerSensitivity and SpecificityBiomarkersBlood ProteinsGlycoproteinsIntegrinsRNA, Messenger

Identifiers

PMID19671866
PMCPMC2766346
OpenAlexW2050856642

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.