Evidence map›Paper›PMID 25003662›Full record

ArticleBritish journal of cancer2014

Phosphorylated protein phosphatase 2A determines poor outcome in patients with metastatic colorectal cancer.

I Cristóbal, R Manso, R Rincón, C Caramés, S Zazo, T G Del Pulgar, A Cebrián, J Madoz-Gúrpide, F Rojo, J García-Foncillas

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

10 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
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  4. Review
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  6. Therapeutic targeting of PP2A.The international journal of biochemistry & cell biology · 2018
    Review
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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

10 authors at 1 institution in 1 country.

I CristóbalTranslational Oncology Division, Oncohealth Institute, IIS-Fundacion Jimenez Diaz, UAM, University Hospital 'Fundacion Jimenez Diaz', E-28040 Madrid, Spain.
R MansoPathology Department, University Hospital 'Fundacion Jimenez Diaz', Autonomous University of Madrid, E-28040 Madrid, Spain.
R RincónTranslational Oncology Division, Oncohealth Institute, IIS-Fundacion Jimenez Diaz, UAM, University Hospital 'Fundacion Jimenez Diaz', E-28040 Madrid, Spain.
C CaramésTranslational Oncology Division, Oncohealth Institute, IIS-Fundacion Jimenez Diaz, UAM, University Hospital 'Fundacion Jimenez Diaz', E-28040 Madrid, Spain.
S ZazoPathology Department, University Hospital 'Fundacion Jimenez Diaz', Autonomous University of Madrid, E-28040 Madrid, Spain.
T G Del PulgarTranslational Oncology Division, Oncohealth Institute, IIS-Fundacion Jimenez Diaz, UAM, University Hospital 'Fundacion Jimenez Diaz', E-28040 Madrid, Spain.
A CebriánTranslational Oncology Division, Oncohealth Institute, IIS-Fundacion Jimenez Diaz, UAM, University Hospital 'Fundacion Jimenez Diaz', E-28040 Madrid, Spain.
J Madoz-GúrpidePathology Department, University Hospital 'Fundacion Jimenez Diaz', Autonomous University of Madrid, E-28040 Madrid, Spain.
F RojoPathology Department, University Hospital 'Fundacion Jimenez Diaz', Autonomous University of Madrid, E-28040 Madrid, Spain.
J García-FoncillasTranslational Oncology Division, Oncohealth Institute, IIS-Fundacion Jimenez Diaz, UAM, University Hospital 'Fundacion Jimenez Diaz', E-28040 Madrid, Spain.
Hospital Universitario Fundación Jiménez Díaz · ES

Funding

NIMHD NIH HHS L60 MD002344
6 · The paper itself

Abstract

backgroundProtein phosphatase 2A (PP2A) is a tumour suppressor frequently inactivated in human cancer and its tyrosine-307 phosphorylation has been reported as a molecular inhibitory mechanism.

methodsExpression of phosphorylated PP2A (p-PP2A) was evaluated in 250 metastatic colorectal cancer (CRC) patients. Chi-square, Kaplan-Meier and Cox analyses were used to determine correlations with clinical and molecular parameters and impact on clinical outcomes.

resultsHigh p-PP2A levels were found in 17.2% cases and were associated with ECOG performance status (P=0.001) and presence of synchronous metastasis at diagnosis (P=0.035). This subgroup showed substantially worse overall survival (OS) (median OS, 6.0 vs 26.2 months, P<0.001) and progression-free survival (PFS) (median PFS, 3.8 vs 13.3 months, P<0.001). The prognostic impact of p-PP2A was particularly evident in patients aged <70 years (P<0.001). Multivariate analysis revealed that p-PP2A retained its prognostic impact for OS (hazard ratio 2.7; 95% confidence interval, 1.8-4.1; P<0.001) and PFS (hazard ratio 3.0; 95% confidence interval, 1.8-5.0; P<0.001).

conclusionsPhosphorylated PP2A is an alteration that determines poor outcome in metastatic CRC and represents a novel potential therapeutic target in this disease, thus enabling to define a subgroup of patients who could benefit from future treatments based on PP2A activators.

Indexed as

AgedBiomarkers, TumorColorectal NeoplasmsFemaleHumansKaplan-Meier EstimateLiver NeoplasmsMaleMultivariate AnalysisPhosphoprotein PhosphatasesPhosphoproteinsPhosphorylationProportional Hazards ModelsProtein Phosphatase 2CProtein Processing, Post-TranslationalBiomarkers, TumorPhosphoprotein PhosphatasesPhosphoproteinsProtein Phosphatase 2C

Identifiers

PMID25003662
PMCPMC4134505
OpenAlexW1994180477

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.