Evidence map›Paper›PMID 19805096›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2009

Discovery and validation of colonic tumor-associated proteins via metabolic labeling and stable isotopic dilution.

Edward L Huttlin, Xiaodi Chen, Gregory A Barrett-Wilt, Adrian D Hegeman, Richard B Halberg, Amy C Harms, Michael A Newton, William F Dove, Michael R Sussman

Open access · bronzeAbstract readValidation Study
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

11 citing papers in PubMed, 32 citations in OpenAlex.

  1. Conserved serum protein biomarkers associated with growing early colorectal adenomas.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  2. Article
  3. Review
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  5. Article
  6. Quantitative assessment of the impact of the gut microbiota on lysine epsilon-acetylation of host proteins using gnotobiotic mice.Proceedings of the National Academy of Sciences of the United States of America · 2012
    Article
  7. Article
  8. Article
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  10. In planta changes in protein phosphorylation induced by the plant hormone abscisic acid.Proceedings of the National Academy of Sciences of the United States of America · 2010
    Article
  11. 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

9 authors at 5 institutions in 3 countries.

Edward L HuttlinDepartment of Biochemistry, University of Wisconsin, Madison, WI 53706, USA.
Xiaodi Chen
Gregory A Barrett-Wilt
Adrian D Hegeman
Richard B Halberg
Amy C Harms
Michael A Newton
William F Dove
Michael R Sussman
Biotechnology Research Center · IRCenter for Cancer Research · USInstitute for Medical Informatics and Biostatistics · CHUniversity of Minnesota · USUniversity of Wisconsin–Madison · US

Funding

INSTITUTIONAL CTSA (UW-MADISON): CLINICAL TRIALSUL1RR025011 · NCRR · UNIVERSITY OF WISCONSIN-MADISON · PI DREZNER, MARC KENNETH · 2007 to 2011
$29.5M
BIOTECHNOLOGY TRAINING PROGRAMT32GM008349 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI FOX, BRIAN G · 1989 to 2019
$22.5M
Institutional Training in the Genomic SciencesT32HG002760 · NHGRI · UNIVERSITY OF WISCONSIN-MADISON · PI Qiongshi Lu · 2003 to 2026
$17.7M
GENES CONTROLLING NEOPLASIA OF THE INTESTINAL EPITHELIUMR37CA063677 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI DOVE, WILLIAM FRANKLIN · 1998 to 2008
$6.3M
NCI NIH HHS R37 CA063677NCI NIH HHS R37-CA63677NCRR NIH HHS UL1 RR025011NCRR NIH HHS UL1RR025011NHGRI NIH HHS T32 HG002760NIGMS NIH HHS 5 T32 GM08349NIGMS NIH HHS T32 GM008349
6 · The paper itself

Abstract

The unique biology of a neoplasm is reflected by its distinct molecular profile compared with normal tissue. To understand tumor development better, we have undertaken a quantitative proteomic search for abnormally expressed proteins in colonic tumors from Apc(Min/+) (Min) mice. By raising pairs of Min and wild-type mice on diets derived from natural-abundance or (15)N-labeled algae, we used metabolic labeling to compare protein levels in colonic tumor versus normal tissue. Because metabolic labeling allows internal control throughout sample preparation and analysis, technical error is minimized as compared with in vitro labeling. Several proteins displayed altered expression, and a subset was validated via stable isotopic dilution using synthetic peptide standards. We also compared gene and protein expression among tumor and nontumor tissue, revealing limited correlation. This divergence was especially pronounced for species showing biological change, highlighting the complementary perspectives provided by transcriptomics and proteomics. Our work demonstrates the power of metabolic labeling combined with stable isotopic dilution as an integrated strategy for the identification and validation of differentially expressed proteins using rodent models of human disease.

Indexed as

Adenomatous Polyposis ColiAdenomatous Polyposis Coli ProteinAnimalsChromatography, LiquidColonic NeoplasmsDietDisease Models, AnimalFemaleGene Expression ProfilingHumansIsotope LabelingLinear ModelsMiceMice, Inbred C57BLMutationNeoplasm ProteinsAdenomatous Polyposis Coli ProteinNeoplasm ProteinsNitrogen IsotopesRNA, Messenger

Identifiers

PMID19805096
PMCPMC2761368
OpenAlexW2144861324

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.