Evidence map›Paper›PMID 25781169›Full record

ArticlePloS one2015

Overexpression of periostin in stroma positively associated with aggressive prostate cancer.

Yuan Tian, Caitlin H Choi, Qing Kay Li, Farah B Rahmatpanah, Xin Chen, Sara Ruth Kim, Robert Veltri, David Chia, Zhen Zhang, Dan Mercola and 1 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

29 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Microfluidic-based human prostate-cancer-on-chip.Frontiers in bioengineering and biotechnology · 2024
    Article
  10. Review
  11. Periostin: biology and function in cancer.Cancer cell international · 2022
    Review
  12. Article
  13. Periostin as a key molecule defining desmoplastic environment in colorectal cancer.Virchows Archiv : an international journal of pathology · 2021
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Periostin function in communication with extracellular matrices.Journal of cell communication and signaling · 2018
    Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 1 country.

Yuan TianDepartment of Pathology, Johns Hopkins University, Baltimore, Maryland, United States of America.
Caitlin H ChoiDepartment of Pathology, Johns Hopkins University, Baltimore, Maryland, United States of America.
Qing Kay LiDepartment of Pathology, Johns Hopkins University, Baltimore, Maryland, United States of America.
Farah B RahmatpanahDepartment of Pathology, University of California at Irvine, Irvine, California, United States of America.
Xin ChenDepartment of Pathology, University of California at Irvine, Irvine, California, United States of America.
Sara Ruth KimDepartment of Pathology and Laboratory Medicine, University of California Los Angeles, Los Angeles, California, United States of America.
Robert VeltriDepartment of Pathology, Johns Hopkins University, Baltimore, Maryland, United States of America.
David ChiaDepartment of Pathology and Laboratory Medicine, University of California Los Angeles, Los Angeles, California, United States of America.
Zhen ZhangDepartment of Pathology, Johns Hopkins University, Baltimore, Maryland, United States of America.
Dan MercolaDepartment of Pathology, University of California at Irvine, Irvine, California, United States of America.
Hui ZhangDepartment of Pathology, Johns Hopkins University, Baltimore, Maryland, United States of America.
Johns Hopkins University · USUniversity of California, Irvine · USUniversity of California, Los Angeles · US

Funding

Shared Resource CoresP01HL107153 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI HART, GERALD WARREN · 2011 to 2017
$16.8M
Proteome Characterization Center: A Genoproteomics Pipeline for Cance ResearchU24CA160036 · NCI · JOHNS HOPKINS UNIVERSITY · PI CHAN, DANIEL WANYUI, ZHANG, HUI · 2011 to 2016
$10.7M
CARCINOGENESIST32CA009054 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI EDINGER, AIMEE L, FRUMAN, DAVID ALEXANDER · 1985 to 2025
$8.6M
The Early Detection Research Network Biomarker Resource Laboratory at UCLAU24CA086366 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CHIA, DAVID S. · 2000 to 2014
$7.3M
Glycoprotein biomarkers for the early detection of aggressive prostate cancerU01CA152813 · NCI · JOHNS HOPKINS UNIVERSITY · PI ZHANG, HUI · 2010 to 2021
$6.2M
NCI NIH HHS CA86366NCI NIH HHS T32 CA009054NCI NIH HHS U01 CA152813NCI NIH HHS U01CA152813NCI NIH HHS U24 CA086366NCI NIH HHS U24 CA160036NHLBI NIH HHS P01 HL107153
6 · The paper itself

Abstract

backgroundPeriostin is an important extracellular matrix protein involved in cell development and adhesion. Previously, we identified periostin to be up-regulated in aggressive prostate cancer (CaP) using quantitative glycoproteomics and mass spectrometry. The expression of periostin was further evaluated in primary radical prostatectomy (RP) prostate tumors and adjacent non-tumorous prostate tissues using immunohistochemistry (IHC). Our IHC results revealed a low background periostin levels in the adjacent non-tumorous prostate tissues, but overexpressed periostin levels in the peritumoral stroma of primary CaP tumors.

methodsIn this study, periostin expression in CaP was further examined on multiple tissue microarrays (TMAs), which were conducted in four laboratories. To achieve consistent staining, all TMAs were stained with same protocol and scored by same image computation tool to determine the total periostin staining intensities. The TMAs were further scored by pathologists to characterize the stromal staining and epithelial staining.

resultsThe periostin staining was observed mainly in peritumoral stromal cells and in some cases in tumor epithelial cells though the stronger staining was found in peritumoral stromal cells. Both periostin stromal staining and epithelial staining can differentiate BPH from CaP including low grade CaP (Gleason score ≤6), with significant p-value of 2.2e-16 and 0.001, respectively. Periostin epithelial staining differentiated PIN from low grade CaP (Gleason score ≤6) (p=0.001), while periostin stromal staining differentiated low grade Cap (Gleason score ≤6) from high grade Cap (Gleason score ≤6) (p=1.7e-05). In addition, a positive correlation between total periostin staining and Gleason score was observed (r=0.87, p=0.002).

conclusionsThe results showed that periostin staining was positively correlated with increasing Gleason score and the aggressiveness of prostate disease.

Indexed as

Gene Expression Regulation, NeoplasticCell Adhesion MoleculesHumansImmunohistochemistryMaleNeoplasm ProteinsProstatic NeoplasmsStromal CellsTissue Array AnalysisCell Adhesion MoleculesNeoplasm ProteinsPOSTN protein, human

Identifiers

PMID25781169
PMCPMC4362940
OpenAlexW2023306972

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.