Evidence map›Paper›PMID 19124481›Full record

ArticleCancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology2009

The elevated expression of a mismatch repair protein is a predictor for biochemical recurrence after radical prostatectomy.

Alixanna M Norris, Michael Gentry, Donna M Peehl, Ralph D'Agostino, Karin D Scarpinato

Open access · bronzeAbstract read
In one paragraph

Article in Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2009. 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
1.4field-weighted citation impact, top 19% 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, 21 citations in OpenAlex.

  1. Article
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  9. Article
  10. Review
  11. Mismatch repair system in endometriotic tissue and eutopic endometrium of unaffected women.International journal of clinical and experimental pathology · 2015
    Article
  12. Article
  13. Male reproductive health and prostate cancer risk.Current opinion in urology · 2011
    Review
  14. Population-based study of the association of variants in mismatch repair genes with prostate cancer risk and outcomes.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2010
    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

5 authors at 4 institutions in 2 countries.

Alixanna M NorrisDepartment of Medicine, Dartmouth-Hitchcock Medical Center & Norris Cotton Comprehensive Cancer Center, Lebanon, New Hampshire, USA.
Michael Gentry
Donna M Peehl
Ralph D'Agostino
Karin D Scarpinato
Wake Forest University · USCentre for Cancer Biology · AUDartmouth–Hitchcock Medical Center · USPalo Alto University · US

Funding

Repair Proteins: Interface between Cell Death &SurvivalR01CA101829 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI SCARPINATO, KARIN D. · 2005 to 2009
$1.2M
NCI NIH HHS R01 CA101829
6 · The paper itself

Abstract

purposeThe inability to predict clinical outcome of prostate cancer is a major impediment to effective treatment decisions and patient counseling. New markers of recurrence are needed to improve the accuracy of risk assessment and treatment of prostate cancer. Our previous studies identified a mismatch repair protein, PMS2, to be elevated in prostate cancer; here, we investigate the prognostic potential of this marker. We hypothesized that the elevation of PMS2 would correlate with disease outcome. EXPERIMENTAL

designRetrospective quantitative immunohistochemistry was done to measure PMS2 in high-grade cancers of 166 men treated by radical prostatectomy with a biochemical recurrence rate of 56%. Associations between PMS2 levels, pathologic variables, and biochemical recurrence over time were determined.

resultsThe mean level of PMS2 protein was consistently higher in both cancer-associated benign epithelium and cancer cells of patients who recurred, compared with nonrecurrent patients. PMS2 was an independent predictor of time-to-recurrence in Cox multivariate analyses and significantly stratified patients based on outcome. PMS2 was able to improve the sensitivity of total percent Gleason 4/5 as a risk factor for recurrence in this cohort.

conclusionsPMS2 protein levels were shown to be a predictor of time-to-recurrence after surgery. This study is the first to document that the elevation of a mismatch repair protein negatively correlates with prognosis and has implications in patient diagnosis and molecular profiling.

Indexed as

DNA Mismatch RepairAdenosine TriphosphatasesAdultAgedBiomarkers, TumorDNA-Binding ProteinsDNA Repair EnzymesHumansImmunohistochemistryMaleMiddle AgedMismatch Repair Endonuclease PMS2Neoplasm Recurrence, LocalPredictive Value of TestsPrognosisProportional Hazards ModelsAdenosine TriphosphatasesBiomarkers, TumorDNA-Binding ProteinsDNA Repair EnzymesMismatch Repair Endonuclease PMS2PMS2 protein, human

Identifiers

PMID19124481
PMCPMC2701238
OpenAlexW2109812096

What OpenQuestion holds

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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.