Evidence map›Paper›PMID 27575585›Full record

ArticleAnalytical chemistry2016

Complementary Glycomic Analyses of Sera Derived from Colorectal Cancer Patients by MALDI-TOF-MS and Microchip Electrophoresis.

Christa M Snyder, William R Alley, Margit I Campos, Martin Svoboda, John A Goetz, Jaqueline A Vasseur, Stephen C Jacobson, Milos V Novotny

Abstract read
In one paragraph

Article in Analytical chemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
5.4field-weighted citation impact, top 4% 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

24 citing papers in PubMed, 51 citations in OpenAlex.

  1. Article
  2. The Human BloodJACS Au · 2024
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Clinical application of quantitative glycomics.Expert review of proteomics · 2018
    Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Review
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.

Christa M SnyderDepartment of Chemistry, Indiana University , Bloomington, Indiana 47405, United States.
William R AlleyDepartment of Chemistry, Indiana University , Bloomington, Indiana 47405, United States.
Margit I CamposDepartment of Chemistry, Indiana University , Bloomington, Indiana 47405, United States.
Martin SvobodaDepartment of Chemistry, Indiana University , Bloomington, Indiana 47405, United States.
John A GoetzDepartment of Chemistry, Indiana University , Bloomington, Indiana 47405, United States.
Jaqueline A VasseurDepartment of Chemistry, Indiana University , Bloomington, Indiana 47405, United States.
Stephen C JacobsonDepartment of Chemistry, Indiana University , Bloomington, Indiana 47405, United States.
Milos V NovotnyDepartment of Chemistry, Indiana University , Bloomington, Indiana 47405, United States.
Indiana University Bloomington · US

Funding

ULTRASENSITIVE METHODS FOR GLYCOCONJUGATE ANALYSISR01GM024349 · NIGMS · TRUSTEES OF INDIANA UNIVERSITY · PI NOVOTNY, MILOS · 1985 to 2014
$2.9M
Early Cancer Detection & Prognosis through GlycomicsU01CA128535 · NCI · TRUSTEES OF INDIANA UNIVERSITY · PI NOVOTNY, MILOS · 2007 to 2011
$1.9M
Microfluidic Devices for Cancer Screening by N-Glycan AnalysisR01GM106084 · NIGMS · TRUSTEES OF INDIANA UNIVERSITY · PI JACOBSON, STEPHEN C · 2014 to 2017
$1.2M
NCI NIH HHS U01 CA128535NIGMS NIH HHS R01 GM024349NIGMS NIH HHS R01 GM106084
6 · The paper itself

Abstract

Colorectal cancer is the fourth most prevalent cancer in the United States, yet there are no reliable noninvasive early screening methods available. Serum-based glycomic profiling has the necessary sensitivity and specificity to distinguish disease states and provide diagnostic potential for this deadly form of cancer. We applied microchip electrophoresis and MALDI-TOF-MS-based glycomic procedures to 20 control serum samples and 42 samples provided by patients diagnosed with colorectal cancer. Within the identified glycans, the position of fucose units was located to quantitate possible changes of fucosyl isomeric species associated with the pathological condition. MALDI-MS data revealed several fucosylated tri- and tetra-antennary glycans which were significantly elevated in their abundance levels in the cancer samples and distinguished the control samples from the colorectal cancer cohort in the comprehensive profiles. When compared to other cancers studied previously, some unique changes appear to be associated with colorectal cancer, being primarily associated with fucosyl isomers. Through MS and microchip electrophoresis-based glycomic methods, several potential biomarkers were identified to aid in the diagnosis and differentiation of colorectal cancer. With its unique capability to resolve isomers, microchip electrophoresis can yield complementary analytical information to MS-based profiling.

Indexed as

Electrophoresis, MicrochipGlycomicsColorectal NeoplasmsHumansPolysaccharidesSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationPolysaccharides

Identifiers

PMID27575585
PMCPMC5097869
OpenAlexW2516486789

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.