Evidence map›Paper›PMID 25077556›Full record

ArticleJournal of proteome research2014

LC-MS profiling of N-Glycans derived from human serum samples for biomarker discovery in hepatocellular carcinoma.

Tsung-Heng Tsai, Minkun Wang, Cristina Di Poto, Yunli Hu, Shiyue Zhou, Yi Zhao, Rency S Varghese, Yue Luo, Mahlet G Tadesse, Dina Hazem Ziada and 4 more

Abstract readComparative Study
In one paragraph

Article in Journal of proteome research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

26 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. LC-MS/MS Isomeric Profiling ofBiomolecules · 2022
    Article
  6. Review
  7. Clinically Viable Assay for Monitoring Uromodulin Glycosylation.Journal of the American Society for Mass Spectrometry · 2021
    Article
  8. Review
  9. Article
  10. 8-plex LC-MS/MS Analysis of PermethylatedAnalytical chemistry · 2019
    Article
  11. Review
  12. Review
  13. Clinical application of quantitative glycomics.Expert review of proteomics · 2018
    Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. 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

14 authors at 5 institutions in 2 countries.

Tsung-Heng TsaiDepartment of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University Medical Center , Washington, DC 20057, United States.
Minkun Wang
Cristina Di Poto
Yunli Hu
Shiyue Zhou
Yi Zhao
Rency S Varghese
Yue Luo
Mahlet G Tadesse
Dina Hazem Ziada
Chirag S Desai
Kirti Shetty
Yehia Mechref
Habtom W Ressom
Georgetown University · USGeorgetown University Medical Center · USTexas Tech University · USMedStar Georgetown University Hospital · USTanta University Hospital · EG

Funding

Sensitive and Quantitative MS-bases Glycomic Mapping PlatformR01GM112490 · NIGMS · TEXAS TECH UNIVERSITY · PI MECHREF, YEHIA · 2014 to 2024
$3.2M
Analysis of LC-MS data to identify peptide and glycan biomarkers for hepatocellulR01CA143420 · NCI · GEORGETOWN UNIVERSITY · PI RESSOM, HABTOM W · 2010 to 2014
$1.4M
Quantitative analysis of LC-MS data for peptide and glycan biomarker discoveryR01GM086746 · NIGMS · GEORGETOWN UNIVERSITY · PI RESSOM, HABTOM W · 2010 to 2014
$1.3M
NCI NIH HHS R01 CA143420NIGMS NIH HHS R01 GM086746NIGMS NIH HHS R01 GM112490
6 · The paper itself

Abstract

Defining clinically relevant biomarkers for early stage hepatocellular carcinoma (HCC) in a high-risk population of cirrhotic patients has potentially far-reaching implications for disease management and patient health. Changes in glycan levels have been associated with the onset of numerous diseases including cancer. In the present study, we used liquid chromatography coupled with electrospray ionization mass spectrometry (LC-ESI-MS) to analyze N-glycans in sera from 183 participants recruited in Egypt and the U.S. and identified candidate biomarkers that distinguish HCC cases from cirrhotic controls. N-Glycans were released from serum proteins and permethylated prior to the LC-ESI-MS analysis. Through two complementary LC-ESI-MS quantitation approaches, global profiling and targeted quantitation, we identified 11 N-glycans with statistically significant differences between HCC cases and cirrhotic controls. These glycans can further be categorized into four structurally related clusters, matching closely with the implications of important glycosyltransferases in cancer progression and metastasis. The results of this study illustrate the power of the integrative approach combining complementary LC-ESI-MS based quantitation approaches to investigate changes in N-glycan levels between HCC cases and patients with liver cirrhosis.

Indexed as

Biomarkers, TumorCarcinoma, HepatocellularChromatography, LiquidEgyptGene Expression ProfilingHumansLiver CirrhosisLiver NeoplasmsMass SpectrometryPolysaccharidesUnited StatesBiomarkers, TumorPolysaccharidescancer biomarker discoveryglycomicshepatocellular carcinomaliver cirrhosismass spectrometrymultiple reaction monitoring

Identifiers

PMID25077556
PMCPMC4227556
OpenAlexW2315438426

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.