Evidence map›Paper›PMID 25972242›Full record

ArticleEndocrine-related cancer2015

Expression of ERG protein in prostate cancer: variability and biological correlates.

Gustavo Ayala, Anna Frolov, Deyali Chatterjee, Dandan He, Susan Hilsenbeck, Michael Ittmann

Open access · bronzeAbstract read
In one paragraph

Article in Endocrine-related cancer, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed, 28 citations in OpenAlex.

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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

6 authors at 2 institutions in 1 country.

Gustavo AyalaDepartment of Pathology and Laboratory MedicineUniversity of Texas Health Sciences Center Medical School, Houston, Texas, USADan L. Duncan Cancer CenterHouston, Texas, USADepartment of Pathology and ImmunologyBaylor College of Medicine, One Baylor Plaza, Houston, Texas 77030, USADepartment of Veterans AffairsMichael E. DeBakey VA Medical Center, Houston, Texas 77030, USA.
Anna FrolovDepartment of Pathology and Laboratory MedicineUniversity of Texas Health Sciences Center Medical School, Houston, Texas, USADan L. Duncan Cancer CenterHouston, Texas, USADepartment of Pathology and ImmunologyBaylor College of Medicine, One Baylor Plaza, Houston, Texas 77030, USADepartment of Veterans AffairsMichael E. DeBakey VA Medical Center, Houston, Texas 77030, USA Department of Pathology and Laboratory MedicineUniversity of Texas Health Sciences Center Medical School, Houston, Texas, USADan L. Duncan Cancer CenterHouston, Texas, USADepartment of Pathology and ImmunologyBaylor College of Medicine, One Baylor Plaza, Houston, Texas 77030, USADepartment of Veterans AffairsMichael E. DeBakey VA Medical Center, Houston, Texas 77030, USA.
Deyali ChatterjeeDepartment of Pathology and Laboratory MedicineUniversity of Texas Health Sciences Center Medical School, Houston, Texas, USADan L. Duncan Cancer CenterHouston, Texas, USADepartment of Pathology and ImmunologyBaylor College of Medicine, One Baylor Plaza, Houston, Texas 77030, USADepartment of Veterans AffairsMichael E. DeBakey VA Medical Center, Houston, Texas 77030, USA.
Dandan HeDepartment of Pathology and Laboratory MedicineUniversity of Texas Health Sciences Center Medical School, Houston, Texas, USADan L. Duncan Cancer CenterHouston, Texas, USADepartment of Pathology and ImmunologyBaylor College of Medicine, One Baylor Plaza, Houston, Texas 77030, USADepartment of Veterans AffairsMichael E. DeBakey VA Medical Center, Houston, Texas 77030, USA.
Susan HilsenbeckDepartment of Pathology and Laboratory MedicineUniversity of Texas Health Sciences Center Medical School, Houston, Texas, USADan L. Duncan Cancer CenterHouston, Texas, USADepartment of Pathology and ImmunologyBaylor College of Medicine, One Baylor Plaza, Houston, Texas 77030, USADepartment of Veterans AffairsMichael E. DeBakey VA Medical Center, Houston, Texas 77030, USA.
Michael IttmannDepartment of Pathology and Laboratory MedicineUniversity of Texas Health Sciences Center Medical School, Houston, Texas, USADan L. Duncan Cancer CenterHouston, Texas, USADepartment of Pathology and ImmunologyBaylor College of Medicine, One Baylor Plaza, Houston, Texas 77030, USADepartment of Veterans AffairsMichael E. DeBakey VA Medical Center, Houston, Texas 77030, USA Department of Pathology and Laboratory MedicineUniversity of Texas Health Sciences Center Medical School, Houston, Texas, USADan L. Duncan Cancer CenterHouston, Texas, USADepartment of Pathology and ImmunologyBaylor College of Medicine, One Baylor Plaza, Houston, Texas 77030, USADepartment of Veterans AffairsMichael E. DeBakey VA Medical Center, Houston, Texas 77030, USA mittmann@bcm.edu.
Michael E. DeBakey VA Medical Center · USDan L Duncan Comprehensive Cancer Center

Funding

Tumor BiologyP30CA125123 · NCI · BAYLOR COLLEGE OF MEDICINE · PI Michael M Ittmann · 2007 to 2026
$73.9M
Role of FGFR1 signaling in distinct cell lineages in prostate cancer progresssionU01CA141497 · NCI · BAYLOR COLLEGE OF MEDICINE · PI ITTMANN, MICHAEL M · 2009 to 2013
$3.4M
Comprehensive Tumor Microenvironment Based Prediction Models in Prostate CancerR01CA140734 · NCI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI AYALA, GUSTAVO ENRIQUE · 2011 to 2015
$1.5M
NCI NIH HHS P30 CA125123NCI NIH HHS R01 CA140734NCI NIH HHS R01CA140734NCI NIH HHS U01 CA141497
6 · The paper itself

Abstract

Prostate cancer is the second leading cause of cancer-related death of men in the USA. The TMPRSS2/ERG (T/E) fusion gene is present in approximately 50% of prostate cancers and promotes tumor progression in vivo. The presence of the T/E fusion gene is strongly associated with the expression of ERG protein, but emerging evidence indicates a significant interfocal and intrafocal variability in the levels of ERG protein expression. We therefore analyzed ERG protein expression by image analysis to objectively quantitate the extent of such heterogeneity, and confirmed significant interfocal and intrafocal variability of ERG protein expression levels in cancer expressing ERG. To define the pathways associated with ERG and its variable expression in prostate cancer, we have analyzed the correlations of ERG expression, as evaluated by immunohistochemistry, with 46 key proteins associated with signal transduction, transcriptional control, and other processes using a large tissue microarray with more than 500 prostate cancers. We found a significant correlation of ERG expression with the markers of activation of the PI3K, MYC, and NFκB pathways, which had previously been linked directly or indirectly to ERG expression. We have also identified significant correlations with novel proteins that have not been previously linked to ERG expression, including serum response factor, the p160 coactivator SRC1, and Sprouty1. Notably, SKP2 only correlated with a high level of ERG protein expression. Thus ERG expression is variable in prostate cancer and is associated with activation of multiple pathways and proteins including several potentially targetable pathways.

Indexed as

Biomarkers, TumorHumansImmunohistochemistryMaleProstatic NeoplasmsSerine EndopeptidasesTissue Array AnalysisBiomarkers, TumorSerine EndopeptidasesTMPRSS2 protein, humanMYCNFκBprostate cancerPTENTMPRSS2/ERG

Identifiers

PMID25972242
PMCPMC4432248
OpenAlexW1917376867

What Socratic 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 Socratic graph.