Evidence map›Paper›PMID 23300999›Full record

ArticlePloS one2013

Wrangling phosphoproteomic data to elucidate cancer signaling pathways.

Mark L Grimes, Wan-Jui Lee, Laurens van der Maaten, Paul Shannon

Abstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
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  8. T-Cell Exhaustion Signatures Vary with Tumor Type and Are Severe in Glioblastoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2018
    Article
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  11. 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

4 authors.

Mark L GrimesDivision of Biological Sciences, University of Montana, Missoula, Montana, United States of America.
Wan-Jui Lee
Laurens van der Maaten
Paul Shannon

Funding

Understanding the molecular mechanism of pathogenesis of prion diseasesP20RR015583 · NCRR · UNIVERSITY OF MONTANA · PI KAVANAUGH, MICHAEL PATRICK · 2000 to 2009
$17.6M
Receptor Tyrosine Kinase Sorting and Transactivation in EndosomesR15NS070746 · NINDS · UNIVERSITY OF MONTANA · PI GRIMES, MARK LINDSAY · 2010 to 2010
$422k
Membrane Traffic Sorting Mechanisms That Produce TrkA Signaling EndosomesR15NS061303 · NINDS · UNIVERSITY OF MONTANA · PI GRIMES, MARK LINDSAY · 2008 to 2008
$212k
NCRR NIH HHS P20 RR015583NINDS NIH HHS NS061303-01NINDS NIH HHS NS070746-01NINDS NIH HHS R15 NS061303NINDS NIH HHS R15 NS070746
6 · The paper itself

Abstract

The interpretation of biological data sets is essential for generating hypotheses that guide research, yet modern methods of global analysis challenge our ability to discern meaningful patterns and then convey results in a way that can be easily appreciated. Proteomic data is especially challenging because mass spectrometry detectors often miss peptides in complex samples, resulting in sparsely populated data sets. Using the R programming language and techniques from the field of pattern recognition, we have devised methods to resolve and evaluate clusters of proteins related by their pattern of expression in different samples in proteomic data sets. We examined tyrosine phosphoproteomic data from lung cancer samples. We calculated dissimilarities between the proteins based on Pearson or Spearman correlations and on Euclidean distances, whilst dealing with large amounts of missing data. The dissimilarities were then used as feature vectors in clustering and visualization algorithms. The quality of the clusterings and visualizations were evaluated internally based on the primary data and externally based on gene ontology and protein interaction networks. The results show that t-distributed stochastic neighbor embedding (t-SNE) followed by minimum spanning tree methods groups sparse proteomic data into meaningful clusters more effectively than other methods such as k-means and classical multidimensional scaling. Furthermore, our results show that using a combination of Spearman correlation and Euclidean distance as a dissimilarity representation increases the resolution of clusters. Our analyses show that many clusters contain one or more tyrosine kinases and include known effectors as well as proteins with no known interactions. Visualizing these clusters as networks elucidated previously unknown tyrosine kinase signal transduction pathways that drive cancer. Our approach can be applied to other data types, and can be easily adopted because open source software packages are employed.

Indexed as

Cluster AnalysisComputational BiologyData Interpretation, StatisticalGene Expression ProfilingHumansMass SpectrometryNeoplasmsProtein Interaction MapsProtein-Tyrosine KinasesProteomicsSignal TransductionSoftwareStochastic ProcessesProtein-Tyrosine Kinases

Identifiers

PMID23300999
PMCPMC3536783

What OpenQuestion holds

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LicenceCC BY
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.