Evidence map›Paper›PMID 26234767›Full record

ArticleTumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine2015

PP2A inhibition as a novel therapeutic target in castration-resistant prostate cancer.

Paula González-Alonso, Ion Cristóbal, Rebeca Manso, Juan Madoz-Gúrpide, Jesús García-Foncillas, Federico Rojo

Abstract read
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In one paragraph

Article in Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Trial
  2. The next decade of SET: from an oncoprotein to beyond.Journal of molecular cell biology · 2024
    Review
  3. Article
  4. Article
  5. Article
  6. 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

6 authors.

Paula González-AlonsoPathology Department, IIS "Fundación Jiménez Diaz", Avda. Reyes Católicos-2, 28040, Madrid, Spain.
Ion Cristóbal
Rebeca Manso
Juan Madoz-Gúrpide
Jesús García-Foncillas
Federico Rojo

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Protein phosphatase 2A (PP2A) is a well-known tumor suppressor frequently inhibited in human cancer. Alterations affecting PP2A subunits together with the deregulation of endogenous PP2A inhibitors such as CIP2A and SET have been described as contributing mechanisms to inactivate PP2A in prostate cancer. Moreover, recent findings highlight that functional inactivation of PP2A could represent a key event in the acquisition of castration-resistant phenotype and a novel molecular target with high impact at both clinical and therapeutic levels in prostate cancer.

Indexed as

ApoptosisAutoantigensCell ProliferationDNA-Binding ProteinsGene Expression Regulation, NeoplasticHistone ChaperonesHumansIntracellular Signaling Peptides and ProteinsMaleMembrane ProteinsMolecular Targeted TherapyProstatic Neoplasms, Castration-ResistantProtein Phosphatase 2Receptors, AndrogenTranscription FactorsAutoantigensCIP2A protein, humanDNA-Binding ProteinsHistone ChaperonesIntracellular Signaling Peptides and ProteinsMembrane ProteinsProtein Phosphatase 2Receptors, AndrogenSET protein, humanTranscription Factors

Identifiers

What OpenQuestion holds

Textmetadata
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.