Evidence map›Paper›PMID 35925813›Full record

ArticleGlycobiology2022

Modeling and integration of N-glycan biomarkers in a comprehensive biomarker data model.

Daniel F Lyman, Amanda Bell, Alyson Black, Hayley Dingerdissen, Edmund Cauley, Nikhita Gogate, David Liu, Ashia Joseph, Robel Kahsay, Daniel J Crichton and 2 more

Open access · greenAbstract read
In one paragraph

Article in Glycobiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 41% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. 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

12 authors at 3 institutions in 2 countries.

Daniel F LymanThe Department of Biochemistry and Molecular Medicine, Ross Hall, School of Medicine & Health Sciences, The George Washington University, 2300 Eye Street N.W., Washington, DC 20037, USA.ORCID 0000-0001-9333-1455
Amanda BellThe Department of Biochemistry and Molecular Medicine, Ross Hall, School of Medicine & Health Sciences, The George Washington University, 2300 Eye Street N.W., Washington, DC 20037, USA.
Alyson BlackThe McCormick Genomic and Proteomic Center, The Department of Biochemistry and Molecular Medicine, Ross Hall, School of Medicine & Health Sciences, The George Washington University, 2300 Eye Street N.W., Washington, DC 20037, USA.
Hayley DingerdissenThe Department of Biochemistry and Molecular Medicine, Ross Hall, School of Medicine & Health Sciences, The George Washington University, 2300 Eye Street N.W., Washington, DC 20037, USA.ORCID 0000-0002-5323-2927
Edmund CauleyThe Department of Biochemistry and Molecular Medicine, Ross Hall, School of Medicine & Health Sciences, The George Washington University, 2300 Eye Street N.W., Washington, DC 20037, USA.
Nikhita GogateThe Department of Biochemistry and Molecular Medicine, Ross Hall, School of Medicine & Health Sciences, The George Washington University, 2300 Eye Street N.W., Washington, DC 20037, USA.
David LiuNASA Jet Propulsion Laboratory, 4800 Oak Grove Dr., Pasadena, California 91109, USA.
Ashia JosephThe Department of Biochemistry and Molecular Medicine, Ross Hall, School of Medicine & Health Sciences, The George Washington University, 2300 Eye Street N.W., Washington, DC 20037, USA.
Robel KahsayThe Department of Biochemistry and Molecular Medicine, Ross Hall, School of Medicine & Health Sciences, The George Washington University, 2300 Eye Street N.W., Washington, DC 20037, USA.
Daniel J CrichtonNASA Jet Propulsion Laboratory, 4800 Oak Grove Dr., Pasadena, California 91109, USA.
Anand MehtaThe Department of Cell & Molecular Pharmacology, Basic Science Building 358, 173 Ashley Avenue, The Medical University of South Carolina, Charleston, SC 29425, USA.
Raja MazumderThe Department of Biochemistry and Molecular Medicine, Ross Hall, School of Medicine & Health Sciences, The George Washington University, 2300 Eye Street N.W., Washington, DC 20037, USA.
George Washington University · USMedical University of South Carolina · USJet Propulsion Laboratory · US

Funding

South Carolina Clinical & Translational Research Institute (SCTR)UL1TR001450 · NCATS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI BRADY, KATHLEEN T., FLUME, PATRICK A · 2015 to 2024
$41.1M
South Carolina Clinical & Translational Research Institute (SCTR)TL1TR001451 · NCATS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI FEGHALI-BOSTWICK, CAROL A. · 2015 to 2024
$4.6M
Integration of comprehensive cancer mutation and expression-associated data for biomarker evaluation and discoveryU01CA215010 · NCI · GEORGE WASHINGTON UNIVERSITY · PI CRICHTON, DANIEL, MAZUMDER, RAJA · 2017 to 2019
$1.3M
NCATS NIH HHS TL1 TR001451NCATS NIH HHS UL1 TR001450NCI NIH HHS U01 CA215010
6 · The paper itself

Abstract

Molecular biomarkers measure discrete components of biological processes that can contribute to disorders when impaired. Great interest exists in discovering early cancer biomarkers to improve outcomes. Biomarkers represented in a standardized data model, integrated with multi-omics data, may improve the understanding and use of novel biomarkers such as glycans and glycoconjugates. Among altered components in tumorigenesis, N-glycans exhibit substantial biomarker potential, when analyzed with their protein carriers. However, such data are distributed across publications and databases of diverse formats, which hamper their use in research and clinical application. Mass spectrometry measures of 50 N-glycans on 7 serum proteins in liver disease were integrated (as a panel) into a cancer biomarker data model, providing a unique identifier, standard nomenclature, links to glycan resources, and accession and ontology annotations to standard protein, gene, disease, and biomarker information. Data provenance was documented with a standardized United States Food and Drug Administration-supported BioCompute Object. Using the biomarker data model allows the capture of granular information, such as glycans with different levels of abundance in cirrhosis, hepatocellular carcinoma, and transplant groups. Such representation in a standardized data model harmonizes glycomics data in a unified framework, making glycan-protein biomarker data exploration more available to investigators and to other data resources. The biomarker data model we describe can be used by researchers to describe their novel glycan and glycoconjugate biomarkers; it can integrate N-glycan biomarker data with multi-source biomedical data and can foster discovery and insight within a unified data framework for glycan biomarker representation, thereby making the data FAIR (Findable, Accessible, Interoperable, Reusable) (https://www.go-fair.org/fair-principles/).

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsBiomarkersBiomarkers, TumorGlycomicsHumansPolysaccharidesBiomarkersBiomarkers, TumorPolysaccharidescancer biomarker paneldata integrationglyco-informaticsliver diseaseN-linked glycans

Identifiers

PMID35925813
PMCPMC9487899
OpenAlexW4289783315

What OpenQuestion holds

Textmetadata
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.