Evidence map›Paper›PMID 21986994›Full record

ArticleMolecular & cellular proteomics : MCP2011

A quantitative proteomic approach of the different stages of colorectal cancer establishes OLFM4 as a new nonmetastatic tumor marker.

Damien Besson, Aude-Hélène Pavageau, Isabelle Valo, Anthony Bourreau, Audrey Bélanger, Caroline Eymerit-Morin, Alice Moulière, Agnès Chassevent, Michelle Boisdron-Celle, Alain Morel and 6 more

Abstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed, 1 pooled it
–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

53 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Biomarkers of tumor invasiveness in proteomics (Review).International journal of oncology · 2020
    Pooled it
  2. Article
  3. Combinatorial chemistry & high throughput screening · 2026
    Article
  4. Olfactomedin 4 in cancer development and progression.Biochimica et biophysica acta. Reviews on cancer · 2025
    Review
  5. Article
  6. Article
  7. Article
  8. A LGR5 reporter pig model closely resembles human intestine for improved study of stem cells in disease.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2023
    Article
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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

16 authors.

Damien BessonInstitut de Cancérologie de l'Ouest, Paul Papin Cancer Center, INSERM U892, Angers, France.
Aude-Hélène Pavageau
Isabelle Valo
Anthony Bourreau
Audrey Bélanger
Caroline Eymerit-Morin
Alice Moulière
Agnès Chassevent
Michelle Boisdron-Celle
Alain Morel
Jerôme Solassol
Mario Campone
Erick Gamelin
Benjamin Barré
Olivier Coqueret
Catherine Guette

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Expression profiles represent new molecular tools that are useful to characterize the successive steps of tumor progression and the prediction of recurrence or chemotherapy response. In this study, we have used quantitative proteomic analysis to compare different stages of colorectal cancer. A combination of laser microdissection, OFFGEL separation, iTRAQ labeling, and MALDI-TOF/TOF MS was used to explore the proteome of 28 colorectal cancer tissues. Two software packages were used for identification and quantification of differentially expressed proteins: Protein Pilot and iQuantitator. Based on ∼1,190,702 MS/MS spectra, a total of 3138 proteins were identified, which represents the largest database of colorectal cancer realized to date and demonstrates the value of our quantitative proteomic approach. In this way, individual protein expression and variation have been identified for each patient and for each colorectal dysplasia and cancer stage (stages I-IV). A total of 555 proteins presenting a significant fold change were quantified in the different stages, and this differential expression correlated with immunohistochemistry results reported in the Human Protein Atlas database. To identify a candidate biomarker of the early stages of colorectal cancer, we focused our study on secreted proteins. In this way, we identified olfactomedin-4, which was overexpressed in adenomas and in early stages of colorectal tumors. This early stage overexpression was confirmed by immunohistochemistry in 126 paraffin-embedded tissues. Our results also indicate that OLFM4 is regulated by the Ras-NF-κB2 pathway, one of the main oncogenic pathways deregulated in colorectal tumors.

Indexed as

AdenocarcinomaAdenomaAdultAgedAged, 80 and overBiomarkers, TumorCarcinomaColorectal NeoplasmsFemaleGene ExpressionGene Expression Regulation, NeoplasticGlycosylationGranulocyte Colony-Stimulating FactorHT29 CellsHumansLaser Capture MicrodissectionBiomarkers, TumorGranulocyte Colony-Stimulating FactorOLFM4 protein, humanProteomeras Proteins

Identifiers

PMID21986994
PMCPMC3237075

What OpenQuestion holds

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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.