Evidence map›Paper›PMID 30993208›Full record

ArticleNPJ precision oncology2019

Precise definition of PTEN C-terminal epitopes and its implications in clinical oncology.

Janire Mingo, Sandra Luna, Ayman Gaafar, Caroline E Nunes-Xavier, Leire Torices, Lorena Mosteiro, Rebeca Ruiz, Isabel Guerra, Roberto Llarena, Javier C Angulo and 2 more

Open access · goldAbstract read
In one paragraph

Article in NPJ precision oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

15 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Probing the properties of PTEN specific botulinum toxin type E mutants.Journal of neural transmission (Vienna, Austria : 1996) · 2025
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  15. Precise Immunodetection of PTEN Protein in Human Neoplasia.Cold Spring Harbor perspectives in medicine · 2019
    Review
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

12 authors at 7 institutions in 2 countries.

Janire MingoBiocruces-Bizkaia Health Research Institute, Barakaldo, Spain.
Sandra LunaBiocruces-Bizkaia Health Research Institute, Barakaldo, Spain.
Ayman Gaafar2Department of Pathology, Cruces University Hospital, Barakaldo, Spain.ORCID 0000-0003-0324-2251
Caroline E Nunes-XavierBiocruces-Bizkaia Health Research Institute, Barakaldo, Spain.
Leire ToricesBiocruces-Bizkaia Health Research Institute, Barakaldo, Spain.
Lorena Mosteiro2Department of Pathology, Cruces University Hospital, Barakaldo, Spain.
Rebeca RuizDepartment of Pathology, Araba University Hospital, Vitoria, Spain.
Isabel GuerraDepartment of Pathology, Araba University Hospital, Vitoria, Spain.
Roberto Llarena6Department of Urology, Cruces University Hospital, Barakaldo, Spain.
Javier C Angulo7Department of Urology, University Hospital of Getafe, Getafe, Madrid, Spain.
José I LópezBiocruces-Bizkaia Health Research Institute, Barakaldo, Spain.
Rafael PulidoBiocruces-Bizkaia Health Research Institute, Barakaldo, Spain.
BioCruces Health research Institute · ESHospital de Cruces · ESUniversity of the Basque Country · ESHospital Universitario Araba · ESHospital Universitario de Getafe · ESIkerbasque · ESOslo University Hospital · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Anti-PTEN monoclonal antibodies (mAb) are arising as important tools for immunohistochemistry (IHC) and protein quantification routine analysis in clinical oncology. Although an effort has been made to document the reliability of tumor tissue section immunostaining by anti-PTEN mAb, and to standardize their IHC use in research and in the clinical practice, the precise topological and biochemical definition of the epitope recognized by each mAb has been conventionally overlooked. In this study, six commercial anti-PTEN mAb have been validated and characterized for sensitivity and specificity by IHC and FISH, using a set of prostate and urothelial bladder tumor specimens, and by immunoblot, using PTEN positive and PTEN negative human cell lines. Immunoblot precise epitope mapping, performed using recombinant PTEN variants and mutations, revealed that all mAb recognized linear epitopes of 6-11 amino acid length at the PTEN C-terminus. Tumor-associated or disease-associated mutations at the PTEN C-terminus did not affect subcellular localization or PIP3 phosphatase activity of PTEN in cells, although resulted in specific loss of reactivity for some mAb. Furthermore, specific mimicking-phosphorylation mutations at the PTEN C-terminal region also abolished binding of specific mAb. Our study adds new evidence on the relevance of a precise epitope mapping in the validation of anti-PTEN mAb for their use in the clinics. This will be substantial to provide a more accurate diagnosis in clinical oncology based on PTEN protein expression in tumors and biological fluids.

Identifiers

PMID30993208
PMCPMC6465295
OpenAlexW2939521850

What OpenQuestion holds

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LicenceCC BY
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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.