Evidence map›Paper›PMID 22277732›Full record

ArticleCancer prevention research (Philadelphia, Pa.)2012

Increased plasma levels of the APC-interacting protein MAPRE1, LRG1, and IGFBP2 preceding a diagnosis of colorectal cancer in women.

Jon J Ladd, Tina Busald, Melissa M Johnson, Qing Zhang, Sharon J Pitteri, Hong Wang, Dean E Brenner, Paul D Lampe, Raju Kucherlapati, Ziding Feng and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer prevention research (Philadelphia, Pa.), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

55 citing papers in PubMed, 92 citations in OpenAlex.

  1. Article
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  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. LRG1: an emerging player in disease pathogenesis.Journal of biomedical science · 2022
    Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Paradoxical Roles of Leucine-Rich αFrontiers in cell and developmental biology · 2021
    Article
  19. Article
  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

12 authors at 3 institutions in 1 country.

Jon J LaddMolecular Diagnostics Program, Fred Hutchinson Cancer Research Center, 1100 Fairview Avenue North, Seattle, WA 98109, USA. jladd@fhcrc.org
Tina Busald
Melissa M Johnson
Qing Zhang
Sharon J Pitteri
Hong Wang
Dean E Brenner
Paul D Lampe
Raju Kucherlapati
Ziding Feng
Ross L Prentice
Samir M Hanash
University of Michigan–Ann Arbor · USFred Hutch Cancer Center · USHarvard University · US

Funding

Affinity Based Strategies to Fast Track Development of Colon Cancer BiomarkersU01CA152746 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI HANASH, SAMIR M, LAMPE, PAUL D. · 2010 to 2014
$3.1M
Preventive Interventions Leadership U01U01CA141550 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI HANASH, SAMIR M · 2009 to 2013
$2.0M
NCI NIH HHS U01 CA141550NCI NIH HHS U01 CA152746
6 · The paper itself

Abstract

Longitudinal blood collections from cohort studies provide the means to search for proteins associated with disease before clinical diagnosis. We investigated plasma samples from the Women's Health Initiative (WHI) cohort to determine quantitative differences in plasma proteins between subjects subsequently diagnosed with colorectal cancer (CRC) and matched controls that remained cancer-free during the period of follow-up. Proteomic analysis of WHI samples collected before diagnosis of CRC resulted in the identification of six proteins with significantly (P < 0.05) elevated concentrations in cases compared with controls. Proteomic analysis of two CRC cell lines showed that five of the six proteins were produced by cancer cells. Microtubule-associated protein RP/EB family member 1 (MAPRE1), insulin-like growth factor-binding protein 2 (IGFBP2), leucine-rich alpha-2-glycoprotein (LRG1), and carcinoembryonic antigen (CEA) were individually assayed by enzyme linked immunosorbent assay (ELISA) in 58 pairs of newly diagnosed CRC samples and controls and yielded significant elevations (P < 0.05) among cases relative to controls. A combination of these four markers resulted in a receiver operating characteristics curve with an area under the curve value of 0.841 and 57% sensitivity at 95% specificity. This combination rule was tested in an independent set of WHI samples collected within 7 months before diagnosis from cases and matched controls resulting in 41% sensitivity at 95% specificity. A panel consisting of CEA, MAPRE1, IGFBP2, and LRG1 has predictive value in prediagnostic CRC plasmas.

Indexed as

Adenomatous Polyposis Coli ProteinAgedCarcinoembryonic AntigenCell Line, TumorColorectal NeoplasmsDNA Mutational AnalysisEnzyme-Linked Immunosorbent AssayFemaleGlycoproteinsHumansInsulin-Like Growth Factor Binding Protein 2Mass SpectrometryMicrotubule-Associated ProteinsMiddle AgedPeptidesROC CurveAdenomatous Polyposis Coli ProteinCarcinoembryonic AntigenGlycoproteinsInsulin-Like Growth Factor Binding Protein 2LRG1 protein, humanMAPRE1 protein, humanMicrotubule-Associated ProteinsPeptides

Identifiers

PMID22277732
PMCPMC3419141
OpenAlexW2164652793

What OpenQuestion holds

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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.