Evidence map›Paper›PMID 24722062›Full record

ArticleThe American journal of surgical pathology2014

HOXB13 G84E-related familial prostate cancers: a clinical, histologic, and molecular survey.

Steven C Smith, Nallasivam Palanisamy, Kimberly A Zuhlke, Anna M Johnson, Javed Siddiqui, Arul M Chinnaiyan, Lakshmi P Kunju, Kathleen A Cooney, Scott A Tomlins

Abstract read
In one paragraph

Article in The American journal of surgical pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
5.6field-weighted citation impact, top 4% 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

24 citing papers in PubMed, 41 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. The Genomics of Prostate Cancer: A Historic Perspective.Cold Spring Harbor perspectives in medicine · 2019
    Review
  10. Synergistic Interaction ofClinical cancer research : an official journal of the American Association for Cancer Research · 2018
    Article
  11. Review
  12. Article
  13. Histopathology of Prostate Cancer.Cold Spring Harbor perspectives in medicine · 2017
    Review
  14. Genomic Insight into the Role of lncRNA in Cancer Susceptibility.International journal of molecular sciences · 2017
    Review
  15. Article
  16. Article
  17. Article
  18. Inherited Predisposition to Prostate Cancer: From Gene Discovery to Clinical Impact.Transactions of the American Clinical and Climatological Association · 2017
    Article
  19. Article
  20. Familial prostate cancer.Seminars in oncology · 2016
    Article
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

9 authors at 3 institutions in 1 country.

Steven C SmithDepartments of *Pathology §Internal Medicine ¶Urology †Michigan Center for Translational Pathology ‡Comprehensive Cancer Center, University of Michigan Medical School, Ann Arbor, MI ∥Howard Hughes Medical Institute, Chevy Chase, MD.
Nallasivam Palanisamy
Kimberly A Zuhlke
Anna M Johnson
Javed Siddiqui
Arul M Chinnaiyan
Lakshmi P Kunju
Kathleen A Cooney
Scott A Tomlins
Michigan Center for Translational Pathology · USHoward Hughes Medical Institute · USUniversity of Michigan–Ann Arbor · US

Funding

VACCINIA PSA FOR ANDROGEN-MODULATED POST-SURGICAL RECURRENCE OF PROSTATE CANCERP50CA069568 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI COONEY, KATHLEEN A · 1995 to 2013
$31.3M
Prostate Cancer Biomarker and Imaging Validation Alliance: Emory University, University of Alabama Birmingham, and University of Texas SouthwesternU01CA113913 · NCI · EMORY UNIVERSITY · PI Martin G. Sanda · 2005 to 2026
$16.4M
Epitomic Biomarkers of Prostate CancerU01CA111275 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CHINNAIYAN, ARUL M, RUBIN, MARK A. · 2004 to 2015
$6.8M
GENETIC ANALYSIS OF HEREDITARY PROSTATE CANCER FAMILIESR01CA079596 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI COONEY, KATHLEEN A · 1999 to 2009
$3.0M
Molecuar Sub-typing of Prostate Cancer Based on Recurrent Gene FusionsR01CA132874 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CHINNAIYAN, ARUL M · 2009 to 2013
$1.2M
Howard Hughes Medical InstituteNCI NIH HHS P50 CA069568NCI NIH HHS P50CA 069568NCI NIH HHS R01 CA079596NCI NIH HHS R01 CA 132874NCI NIH HHS R01 CA132874NCI NIH HHS R01 CA 79596NCI NIH HHS U01 CA111275NCI NIH HHS U01 CA113913
6 · The paper itself

Abstract

Recent genetic epidemiologic studies identified a germline mutation in the homeobox transcription factor, HOXB13 G84E, which is associated with markedly increased risk for prostate cancer, particularly early-onset hereditary prostate cancer. The histomorphologic and molecular features of cancers arising in such carriers have not been studied. Here, we reviewed prostatectomy specimens from 23 HOXB13 G84E mutation carriers, mapping the total cancer burden by anatomically distinct cancer focus and evaluating morphologic features. We also assessed basic molecular subtypes for all cancer foci (ERG/SPINK1 status) by dual immunohistochemistry staining on full sections. The cohort showed a median age of 58 years, a median serum PSA level of 5.7 ng/mL, and a median of 6 cancer foci (range, 1 to 14) per case. Of evaluable cases, dominant foci were Gleason score 6 in 23%, 3+4=7 in 41%, 4+3=7 in 23%, and ≥8 in 14%; biochemical recurrence was observed in 1 case over a median of 36 months follow-up. Histologic review found a high prevalence of cases showing cancers with a spectrum of features previously described with pseudohyperplastic carcinomas, with 45% of cases showing a dominant focus with such features. Molecular subtyping revealed a strikingly low prevalence of ERG cancer with increased prevalence of SPINK1 cancer (dominant focus ERG 17%, SPINK1 26%, ERG/SPINK1 52%, single ERG/SPINK1 focus 4%). One ERG/SPINK1 dominant focus showed aberrant p63 immunophenotype. In summary, HOXB13 G84E variant-related prostate cancers show frequent pseudohyperplastic-type features and markedly low prevalence of ERG cancers relative to unselected cases and, especially, to early-onset cohorts. These findings suggest that novel molecular pathways may drive disease in HOXB13 G84E carriers.

Indexed as

AdenocarcinomaCarrier ProteinsGenetic Predisposition to DiseaseGerm-Line MutationHomeodomain ProteinsHumansImmunohistochemistryMaleMiddle AgedNeoplasm GradingNeoplasm StagingProstatic NeoplasmsTrans-ActivatorsTranscriptional Regulator ERGTrypsin Inhibitor, Kazal PancreaticCarrier ProteinsERG protein, humanHomeodomain ProteinsHOXB13 protein, humanSPINK1 protein, humanTrans-ActivatorsTranscriptional Regulator ERGTrypsin Inhibitor, Kazal Pancreatic

Identifiers

PMID24722062
PMCPMC3988475
OpenAlexW2016245733

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.