Evidence map›Paper›PMID 19769411›Full record

ArticleJournal of proteome research2009

Differential secreted proteome approach in murine model for candidate biomarker discovery in colon cancer.

Kannan Rangiah, Montri Tippornwong, Vineet Sangar, David Austin, Marie-Pier Tétreault, Anil K Rustgi, Ian A Blair, Kenneth H Yu

Abstract readEvaluation Study
In one paragraph

Article in Journal of proteome research, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

17 citing papers in PubMed, 48 citations in OpenAlex.

  1. Article
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  4. Article
  5. Proteins are potent biomarkers to detect colon cancer progression.Saudi journal of biological sciences · 2017
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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

8 authors at 1 institution in 1 country.

Kannan RangiahCenters for Cancer Pharmacology and Excellence in Environmental Toxicology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104-6160, USA.
Montri Tippornwong
Vineet Sangar
David Austin
Marie-Pier Tétreault
Anil K Rustgi
Ian A Blair
Kenneth H Yu
University of Pennsylvania · US

Funding

UNIVERSITY OF PENNSYLVANIA CAN CTR SUPPORT GRANTP30CA016520 · NCI · UNIVERSITY OF PENNSYLVANIA · PI SHELLEY L BERGER · 1985 to 2026
$222.3M
Translational Research Support CoreP30ES013508 · NIEHS · UNIVERSITY OF PENNSYLVANIA · PI Rebecca A Simmons · 2006 to 2026
$35.3M
The LIN28b-Let7-IMP1 axis in colonic epithelial biologyR01DK056645 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI RUSTGI, ANIL K · 2000 to 2021
$6.8M
FOURIER TRANSFORM MASS SPEC PROTEOMICS AND GENOMICS: SMOKING &TOBACCOS10RR019939 · NCRR · UNIVERSITY OF PENNSYLVANIA · PI BLAIR, IAN ALEXANDER · 2004 to 2004
$772k
NCI NIH HHS P30 CA016520NCRR NIH HHS S10 RR019939NCRR NIH HHS U54 RR023567NIDDK NIH HHS R01 DK056645NIEHS NIH HHS P30 ES013508
6 · The paper itself

Abstract

The complexity and heterogeneity of the plasma proteome have presented significant challenges in the identification of protein changes associated with tumor development. We used cell culture as a model system and identified differentially expressed, secreted proteins which may constitute serological biomarkers. A stable isotope labeling by amino acids in cell culture (SILAC) approach was used to label the entire secreted proteomes of the CT26 murine colon cancer cell line and normal young adult mouse colon (YAMC) cell line, thereby creating a stable isotope labeled proteome (SILAP) standard. This SILAP standard was added to unlabeled murine CT26 colon cancer cell or normal murine YAMC colon epithelial cell secreted proteome samples. A multidimensional approach combining isoelectric focusing (IEF), strong cation exchange (SCX) followed by reversed phase liquid chromatography was used for extensive protein and peptide separation. A total of 614 and 929 proteins were identified from the YAMC and CT26 cell lines, with 418 proteins common to both cell lines. Twenty highly abundant differentially expressed proteins from these groups were selected for liquid chromatography-multiple reaction monitoring/mass spectrometry (LC-MRM/MS) analysis in sera. Differential secretion into the serum was observed for several proteins when Apc(min) mice were compared with control mice. These findings were then confirmed by Western blot analysis.

Indexed as

AnimalsBiological AssayBiomarkersCell Line, TumorChromatography, LiquidColonic NeoplasmsCulture Media, ConditionedHumansMiceMice, Inbred C57BLNeoplasm ProteinsProteomeReproducibility of ResultsTandem Mass SpectrometryBiomarkersCulture Media, ConditionedNeoplasm ProteinsProteome

Identifiers

PMID19769411
PMCPMC2783939
OpenAlexW1996132626

What OpenQuestion holds

Textmetadata
LicenceTDM
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.