Evidence map›Paper›PMID 31784980›Full record

ArticleThe Journal of pathology2020

Proteins in stool as biomarkers for non-invasive detection of colorectal adenomas with high risk of progression.

Malgorzata A Komor, Linda Jw Bosch, Veerle Mh Coupé, Christian Rausch, Thang V Pham, Sander R Piersma, Sandra Mongera, Chris Jj Mulder, Evelien Dekker, Ernst J Kuipers and 6 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of pathology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 2 pooled it
2.5field-weighted citation impact, top 9% 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

32 citing papers in PubMed, 2 syntheses or guidelines pooled it, 49 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. EnterohemorrhagicAIMS microbiology · 2025
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Proteomics techniques in protein biomarker discovery.Quantitative biology (Beijing, China) · 2024
    Review
  12. Review
  13. Article
  14. [Construction of a fecal protein Luminex liquid chip detection system for early diagnosis of colorectal tumors].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2023
    Article
  15. Article
  16. Review
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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 at 4 institutions in 1 country.

Malgorzata A KomorDepartment of Pathology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.ORCID 0000-0002-2983-1639
Linda Jw BoschDepartment of Pathology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Veerle Mh CoupéDepartment of Epidemiology and Biostatistics, Amsterdam UMC, VU University Medical Center, Amsterdam, The Netherlands.
Christian RauschDepartment of Pathology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Thang V PhamDepartment of Medical Oncology, Amsterdam UMC, VU University Medical Center, Amsterdam, The Netherlands.
Sander R PiersmaDepartment of Medical Oncology, Amsterdam UMC, VU University Medical Center, Amsterdam, The Netherlands.
Sandra MongeraDepartment of Pathology, Amsterdam UMC, VU University Medical Center, Amsterdam, The Netherlands.
Chris Jj MulderDepartment of Gastroenterology and Hepatology, Amsterdam UMC, VU University Medical Center, Amsterdam, The Netherlands.
Evelien DekkerDepartment of Gastroenterology and Hepatology, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
Ernst J KuipersDepartment of Gastroenterology and Hepatology, Erasmus MC University Medical Center, Rotterdam, The Netherlands.
Mark A van de WielDepartment of Epidemiology and Biostatistics, Amsterdam UMC, VU University Medical Center, Amsterdam, The Netherlands.
Beatriz CarvalhoDepartment of Pathology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Remond Ja FijnemanDepartment of Pathology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.ORCID 0000-0003-2076-5521
Connie R JimenezDepartment of Medical Oncology, Amsterdam UMC, VU University Medical Center, Amsterdam, The Netherlands.
Gerrit A MeijerDepartment of Pathology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Meike de WitDepartment of Pathology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.ORCID 0000-0003-1850-0831
Amsterdam UMC Location Vrije Universiteit Amsterdam · NLThe Netherlands Cancer Institute · NLAmsterdam Neuroscience · NLErasmus MC · NL

Funding

NRSA Training CoreTL1TR001415 · NCATS · UNIVERSITY OF CALIFORNIA-IRVINE · PI CAIOZZO, VINCENT JAMES, HEAD, ELIZABETH · 2015 to 2023
$4.2M
6 · The paper itself

Abstract

Screening to detect colorectal cancer (CRC) in an early or premalignant state is an effective method to reduce CRC mortality rates. Current stool-based screening tests, e.g. fecal immunochemical test (FIT), have a suboptimal sensitivity for colorectal adenomas and difficulty distinguishing adenomas at high risk of progressing to cancer from those at lower risk. We aimed to identify stool protein biomarker panels that can be used for the early detection of high-risk adenomas and CRC. Proteomics data (LC-MS/MS) were collected on stool samples from adenoma (n = 71) and CRC patients (n = 81) as well as controls (n = 129). Colorectal adenoma tissue samples were characterized by low-coverage whole-genome sequencing to determine their risk of progression based on specific DNA copy number changes. Proteomics data were used for logistic regression modeling to establish protein biomarker panels. In total, 15 of the adenomas (15.8%) were defined as high risk of progressing to cancer. A protein panel, consisting of haptoglobin (Hp), LAMP1, SYNE2, and ANXA6, was identified for the detection of high-risk adenomas (sensitivity of 53% at specificity of 95%). Two panels, one consisting of Hp and LRG1 and one of Hp, LRG1, RBP4, and FN1, were identified for high-risk adenomas and CRCs detection (sensitivity of 66% and 62%, respectively, at specificity of 95%). Validation of Hp as a biomarker for high-risk adenomas and CRCs was performed using an antibody-based assay in FIT samples from a subset of individuals from the discovery series (n = 158) and an independent validation series (n = 795). Hp protein was significantly more abundant in high-risk adenoma FIT samples compared to controls in the discovery (p = 0.036) and the validation series (p = 9e-5). We conclude that Hp, LAMP1, SYNE2, LRG1, RBP4, FN1, and ANXA6 may be of value as stool biomarkers for early detection of high-risk adenomas and CRCs. © 2019 Authors. Journal of Pathology published by John Wiley & Sons Ltd on behalf of Pathological Society of Great Britain and Ireland.

Indexed as

FecesAdenomaBiomarkers, TumorChromatography, LiquidColorectal NeoplasmsDisease ProgressionEarly Detection of CancerHumansProteomicsSensitivity and SpecificityTandem Mass SpectrometryBiomarkers, Tumorbiomarkerscolorectal cancerearly detectionhigh-risk adenomas

Identifiers

PMID31784980
PMCPMC7065084
OpenAlexW2990047946

What OpenQuestion holds

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LicenceCC BY
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.