Evidence map›Paper›PMID 27562498›Full record

ArticleModern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc2016

Loss of PTEN expression in ERG-negative prostate cancer predicts secondary therapies and leads to shorter disease-specific survival time after radical prostatectomy.

Kanerva Lahdensuo, Andrew Erickson, Irena Saarinen, Heikki Seikkula, Johan Lundin, Mikael Lundin, Stig Nordling, Anna Bützow, Hanna Vasarainen, Peter J Boström and 3 more

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In one paragraph

Article in Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

22 citing papers in PubMed, 46 citations in OpenAlex.

  1. Review
  2. Exploring therapeutic applications ofFrontiers in oncology · 2025
    Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. The Movember Global Action Plan 1 (GAP1): Unique Prostate Cancer Tissue Microarray Resource.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2022
    Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. Precise Immunodetection of PTEN Protein in Human Neoplasia.Cold Spring Harbor perspectives in medicine · 2019
    Review
  13. Article
  14. The clinicopathologic significance of Notch3 expression in prostate cancer.International journal of clinical and experimental pathology · 2019
    Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Oncotarget · 2017
    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

13 authors at 6 institutions in 1 country.

Kanerva LahdensuoDepartment of Urology, Meilahti Hospital, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Andrew EricksonInstitute for Molecular Medicine Finland (FIMM), Helsinki, Finland.
Irena SaarinenDepartment of Pathology, University of Turku and Turku University Hospital, Turku, Finland.
Heikki SeikkulaDepartment of Urology, University of Turku and Turku University Hospital, Turku, Finland.
Johan LundinInstitute for Molecular Medicine Finland (FIMM), Helsinki, Finland.
Mikael LundinInstitute for Molecular Medicine Finland (FIMM), Helsinki, Finland.
Stig NordlingDepartment of Pathology, HUSLAB and Medicum, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Anna BützowUnited Medix Laboratories, Pathology, Helsinki, Finland.
Hanna VasarainenDepartment of Urology, Meilahti Hospital, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Peter J BoströmDepartment of Urology, University of Turku and Turku University Hospital, Turku, Finland.
Pekka TaimenDepartment of Pathology, University of Turku and Turku University Hospital, Turku, Finland.
Antti RannikkoDepartment of Urology, Meilahti Hospital, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Tuomas MirttiInstitute for Molecular Medicine Finland (FIMM), Helsinki, Finland.
University of Helsinki · FIInstitute for Molecular Medicine Finland · FITurku University Hospital · FIHelsinki University Hospital · FIUnited Medix Laboratories (Finland) · FIUniversity of Turku · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The clinical course of prostate cancer is highly variable. Current prognostic variables, stage, and Gleason score have limitations in assessing treatment regimens for individual patients, especially in the intermediate-risk group of Gleason score 7. ERG:TMPRSS2 fusion and loss of PTEN are some of the most common genetic alterations in prostate cancer. Immunohistochemistry of PTEN and ERG has generated interest as a promising method for more precise outcome prediction but requires further validation in population-based cohorts. We studied the predictive value of ERG and PTEN expression by immunohistochemistry in two large radical prostatectomy cohorts comprising 815 patients with extensive follow-up information. Clinical end points were initiation of secondary therapy, overall survival, and disease-specific survival. Predictions of clinical outcomes were also assessed according to androgen receptor (AR) activity. PTEN loss, especially in ERG-negative cancers, predicted initiation of secondary treatments and shortened disease-specific survival time, as well as stratifying Gleason score 7 patients into different prognostic groups with regard to secondary treatments and disease-specific survival. High AR immunoreactivity in ERG-negative cancers with PTEN loss predicted worse disease-specific survival. We also observed that in Gleason score 7 ERG-negative cases with PTEN loss and high AR expression have significantly shorter disease-specific survival time compared with ERG-positive cases. Our conclusion is that loss of PTEN is a strong determining factor for shorter disease-specific survival time and initiation of secondary therapies after radical prostatectomy. The predictive value of PTEN immunoreactivity is further accentuated in ERG-negative cancers with high AR expression. Negative PTEN expression, accompanied by ERG status, can be used to stratify patients with Gleason score 7 into different survival groups. Assessment of PTEN and ERG status could provide an additional tool for initial diagnostics when determining the prognosis and subsequent follow-up regimen for patients treated by radical prostatectomy.

Indexed as

AdultAgedBiomarkers, TumorDisease-Free SurvivalHumansMaleMiddle AgedNeoplasm Recurrence, LocalPredictive Value of TestsPrognosisProstatectomyProstatic NeoplasmsPTEN PhosphohydrolaseTranscriptional Regulator ERGBiomarkers, TumorERG protein, humanPTEN PhosphohydrolasePTEN protein, humanTranscriptional Regulator ERG

Identifiers

PMID27562498
OpenAlexW2515442448

What OpenQuestion holds

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Read underepoch 390

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.