Evidence map›Paper›PMID 21967744›Full record

ArticleJournal of clinical bioinformatics2011

Technical phosphoproteomic and bioinformatic tools useful in cancer research.

Elena López, Jan-Jaap Wesselink, Isabel López, Jesús Mendieta, Paulino Gómez-Puertas, Sarbelio Rodríguez Muñoz

Abstract read
In one paragraph

Article in Journal of clinical bioinformatics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. A proteomic approach to obesity and type 2 diabetes.Journal of cellular and molecular medicine · 2015
    Review
  3. Article
  4. Article
  5. Phosphoproteomics and lung cancer research.International journal of molecular sciences · 2012
    Review
  6. Functional phosphoproteomic mass spectrometry-based approaches.Clinical and translational medicine · 2012
    Article
  7. Article
  8. Article
  9. 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.

Elena LópezCentro de Investigación i+12 del Hospital Universitario 12 de Octubre, Avda de Córdoba s/n Madrid, 28041, Spain.
Jan-Jaap WesselinkCentro de Biología Molecular "Severo Ochoa" (CSIC-UAM) Campus de Cantoblanco, c/Nicolás Cabrera, 1, 28049 Madrid, Spain.
Isabel LópezServicio de Hematología Hospital QUIRÓN, Madrid, Diego de Velázquez 1 28223, Pozuelo Madrid Spain.
Jesús MendietaCentro de Biología Molecular "Severo Ochoa" (CSIC-UAM) Campus de Cantoblanco, c/Nicolás Cabrera, 1, 28049 Madrid, Spain.
Paulino Gómez-Puertas *Centro de Biología Molecular "Severo Ochoa" (CSIC-UAM) Campus de Cantoblanco, c/Nicolás Cabrera, 1, 28049 Madrid, Spain.
Sarbelio Rodríguez Muñoz *Servicio de Digestivo, Hospital Universitario 12 Octubre, Avda de Córdoba s/n Madrid, 28041, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Reversible protein phosphorylation is one of the most important forms of cellular regulation. Thus, phosphoproteomic analysis of protein phosphorylation in cells is a powerful tool to evaluate cell functional status. The importance of protein kinase-regulated signal transduction pathways in human cancer has led to the development of drugs that inhibit protein kinases at the apex or intermediary levels of these pathways. Phosphoproteomic analysis of these signalling pathways will provide important insights for operation and connectivity of these pathways to facilitate identification of the best targets for cancer therapies. Enrichment of phosphorylated proteins or peptides from tissue or bodily fluid samples is required. The application of technologies such as phosphoenrichments, mass spectrometry (MS) coupled to bioinformatics tools is crucial for the identification and quantification of protein phosphorylation sites for advancing in such relevant clinical research. A combination of different phosphopeptide enrichments, quantitative techniques and bioinformatic tools is necessary to achieve good phospho-regulation data and good structural analysis of protein studies. The current and most useful proteomics and bioinformatics techniques will be explained with research examples. Our aim in this article is to be helpful for cancer research via detailing proteomics and bioinformatic tools.

Identifiers

PMID21967744
PMCPMC3195713

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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.