Evidence map›Paper›PMID 30030909›Full record

ArticleCancer medicine2018

Serum type XVI collagen is associated with colorectal cancer and ulcerative colitis indicating a pathological role in gastrointestinal disorders.

Christina Jensen, Signe H Nielsen, Joachim H Mortensen, Jens Kjeldsen, Lone G Klinge, Aleksander Krag, Henrik Harling, Lars N Jørgensen, Morten A Karsdal, Nicholas Willumsen

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

16 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. The Multifaced Role of Collagen in Cancer Development and Progression.International journal of molecular sciences · 2024
    Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Extracellular Matrix Biomarkers in Colorectal Cancer.International journal of molecular sciences · 2021
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. 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

10 authors at 3 institutions in 1 country.

Christina JensenBiomarkers & Research, Nordic Bioscience, Herlev, Denmark.ORCID 0000-0002-3485-7307
Signe H NielsenBiomarkers & Research, Nordic Bioscience, Herlev, Denmark.
Joachim H MortensenBiomarkers & Research, Nordic Bioscience, Herlev, Denmark.
Jens KjeldsenDepartment of Medical Gastroenterology, Odense University Hospital, Odense, Denmark.
Lone G KlingeDepartment of Medical Gastroenterology, Odense University Hospital, Odense, Denmark.
Aleksander KragDepartment of Medical Gastroenterology, Odense University Hospital, Odense, Denmark.
Henrik HarlingDigestive Disease Center, Bispebjerg Hospital, University of Copenhagen, Copenhagen, Denmark.
Lars N JørgensenDigestive Disease Center, Bispebjerg Hospital, University of Copenhagen, Copenhagen, Denmark.
Morten A KarsdalBiomarkers & Research, Nordic Bioscience, Herlev, Denmark.
Nicholas WillumsenBiomarkers & Research, Nordic Bioscience, Herlev, Denmark.
Nordic Bioscience (Denmark) · DKOdense University Hospital · DKUniversity of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Altered extracellular matrix (ECM) remodeling is an important part of the pathology of gastrointestinal (GI) disorders. In the intestine, type XVI collagen (col-16) plays a role in pathogenesis by affecting ECM architecture and induce cell invasion. Measuring col-16 in serum may therefore have biomarker potential in GI disorders such as colorectal cancer (CRC) and ulcerative colitis (UC). The aim of this study was to determine whether col-16 can serve as a biomarker for altered ECM remodeling in patients with CRC and UC. A monoclonal antibody was raised against the C-terminal end of col-16 (PRO-C16), and a competitive enzyme-linked immunosorbent assay (ELISA) was developed and technically validated. Levels of PRO-C16 were measured in serum from patients with CRC (before (n = 50) and 3 months after (n = 23) tumor resections), UC (n = 39) and healthy controls (n = 50). The PRO-C16 ELISA was specific toward the C-terminal of col-16. PRO-C16 was significantly elevated both in serum from patients with CRC (P = 0.0026) and UC (P < 0.0001) compared to controls. No difference was detected in levels of PRO-C16 between patients with CRC at baseline and 3 months after tumor resections (P > 0.999). Levels of PRO-C16 identified patients with a GI disorder with a positive predictive value of 0.9 and an odds ratio of 12 (95%CI = 4.5-29.5, P < 0.0001). The newly developed assay detected significantly elevated levels of PRO-C16 in serum from patients with GI disorders compared to controls suggesting its potential as a biomarker in this setting. Future studies are needed to validate these findings.

Indexed as

AdultAgedAged, 80 and overAmino Acid SequenceBiomarkersCase-Control StudiesColitis, UlcerativeCollagenColorectal NeoplasmsEnzyme-Linked Immunosorbent AssayExtracellular MatrixFemaleHumansMaleMiddle AgedModels, BiologicalBiomarkersCOL16A1 protein, humanCollagenPeptidesbiomarkerscollagencolorectal cancerextracellular matrixulcerative colitis

Identifiers

PMID30030909
PMCPMC6144245
OpenAlexW2883862985

What OpenQuestion holds

Textmetadata
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.