Evidence map›Paper›PMID 27462933›Full record

ArticleJournal of proteome research2016

Optimized Protocol for Quantitative Multiple Reaction Monitoring-Based Proteomic Analysis of Formalin-Fixed, Paraffin-Embedded Tissues.

Jacob J Kennedy, Jeffrey R Whiteaker, Regine M Schoenherr, Ping Yan, Kimberly Allison, Melissa Shipley, Melissa Lerch, Andrew N Hoofnagle, Geoffrey Stuart Baird, Amanda G Paulovich

Registry-linked trialAbstract read
In one paragraph

Article in Journal of proteome research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03765450 (Pharmacokinetics of Infliximab and Tumor Necrosis Factor Concentrations in Serum, Stool, and Colonic Mucosa in Acute Severe Ulcerative Colitis), which is not on this map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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.

NCT03765450 active not recruitingnot on this mapstarted 2018, after this paper: background citation

Pharmacokinetics of Infliximab and Tumor Necrosis Factor Concentrations in Serum, Stool, and Colonic Mucosa in Acute Severe Ulcerative Colitis

TypeobservationalSponsorAlimentiv Inc.Ran2018 to 2027Enrolled18ConditionsUlcerative ColitisArmsInfliximab
3 · Its place in the literature

Who cites it

24 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Clinical Proteomics for Solid Organ Tissues.Molecular & cellular proteomics : MCP · 2023
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Clinical potential of mass spectrometry-based proteogenomics.Nature reviews. Clinical oncology · 2019
    Review
  20. 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

10 authors.

Jacob J KennedyClinical Research Division, Fred Hutchinson Cancer Research Center , Seattle, Washington 98109, United States.
Jeffrey R WhiteakerClinical Research Division, Fred Hutchinson Cancer Research Center , Seattle, Washington 98109, United States.
Regine M SchoenherrClinical Research Division, Fred Hutchinson Cancer Research Center , Seattle, Washington 98109, United States.
Ping YanClinical Research Division, Fred Hutchinson Cancer Research Center , Seattle, Washington 98109, United States.
Kimberly AllisonDepartment of Pathology, Stanford University , Stanford, California 94305 United States.
Melissa ShipleyDepartment of Laboratory Medicine, University of Washington , Seattle, Washington 98195 United States.
Melissa LerchDepartment of Laboratory Medicine, University of Washington , Seattle, Washington 98195 United States.
Andrew N HoofnagleDepartment of Laboratory Medicine, University of Washington , Seattle, Washington 98195 United States.
Geoffrey Stuart BairdDepartment of Laboratory Medicine, University of Washington , Seattle, Washington 98195 United States.
Amanda G PaulovichClinical Research Division, Fred Hutchinson Cancer Research Center , Seattle, Washington 98109, United States.

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Eric Collisson · 1985 to 2026
$296.4M
Transform Dissemination and Implementation Science in CTSA ProgramsUL1TR002319 · NCATS · UNIVERSITY OF WASHINGTON · PI John K. Amory · 2017 to 2026
$100.0M
Institute of Translational Health SciencesUL1TR000423 · NCATS · UNIVERSITY OF WASHINGTON · PI DISIS, MARY L. · 2012 to 2016
$49.4M
Proteo-genomic Discovery, Prioritization and Verification of Cancer BiomarkersU24CA160034 · NCI · BROAD INSTITUTE, INC. · PI CARR, STEVEN A, PAULOVICH, AMANDA G · 2011 to 2016
$16.2M
Advanced development of immuno-MRM technology to analyze archived cancer tissuesR33CA173300 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI PAULOVICH, AMANDA G · 2013 to 2015
$1.2M
NCATS NIH HHS UL1 TR000423NCATS NIH HHS UL1 TR002319NCI NIH HHS P30 CA015704NCI NIH HHS R33 CA173300NCI NIH HHS U24 CA160034
6 · The paper itself

Abstract

Despite a clinical, economic, and regulatory imperative to develop companion diagnostics, precious few new biomarkers have been successfully translated into clinical use, due in part to inadequate protein assay technologies to support large-scale testing of hundreds of candidate biomarkers in formalin-fixed paraffin-embedded (FFPE) tissues. Although the feasibility of using targeted, multiple reaction monitoring mass spectrometry (MRM-MS) for quantitative analyses of FFPE tissues has been demonstrated, protocols have not been systematically optimized for robust quantification across a large number of analytes, nor has the performance of peptide immuno-MRM been evaluated. To address this gap, we used a test battery approach coupled to MRM-MS with the addition of stable isotope-labeled standard peptides (targeting 512 analytes) to quantitatively evaluate the performance of three extraction protocols in combination with three trypsin digestion protocols (i.e., nine processes). A process based on RapiGest buffer extraction and urea-based digestion was identified to enable similar quantitation results from FFPE and frozen tissues. Using the optimized protocols for MRM-based analysis of FFPE tissues, median precision was 11.4% (across 249 analytes). There was excellent correlation between measurements made on matched FFPE and frozen tissues, both for direct MRM analysis (R(2) = 0.94) and immuno-MRM (R(2) = 0.89). The optimized process enables highly reproducible, multiplex, standardizable, quantitative MRM in archival tissue specimens.

Indexed as

BiomarkersCellsFormaldehydeHumansIsotope LabelingMass SpectrometryParaffin EmbeddingProteomicsTissue FixationTissue PreservationBiomarkersFormaldehydearchived tissueFFPEimmunoaffinity enrichmentmass spectrometrymultiple reaction monitoringpeptide assaystargeted proteomics

Identifiers

PMID27462933
PMCPMC5017241

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Registered trials

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.