Evidence map›Paper›PMID 37108213›Full record

ArticleInternational journal of molecular sciences2023

Compositional Analysis of Glycosaminoglycans in Different Lung Cancer Types-A Pilot Study.

Domonkos Pál, Gábor Tóth, Simon Sugár, Kata Dorina Fügedi, Dániel Szabó, Ilona Kovalszky, Dávid Papp, Gitta Schlosser, Csaba Tóth, Tamás Tornóczky and 2 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.5field-weighted citation impact, top 12% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

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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

12 authors at 6 institutions in 1 country.

Domonkos PálMS Proteomics Research Group, Research Centre for Natural Sciences, H-1117 Budapest, Hungary.ORCID 0000-0002-0226-0004
Gábor TóthMS Proteomics Research Group, Research Centre for Natural Sciences, H-1117 Budapest, Hungary.ORCID 0000-0003-1428-7906
Simon SugárMS Proteomics Research Group, Research Centre for Natural Sciences, H-1117 Budapest, Hungary.ORCID 0000-0001-9728-5732
Kata Dorina FügediMS Proteomics Research Group, Research Centre for Natural Sciences, H-1117 Budapest, Hungary.
Dániel SzabóMS Proteomics Research Group, Research Centre for Natural Sciences, H-1117 Budapest, Hungary.ORCID 0000-0003-3375-395X
Ilona Kovalszky1st Department of Pathology and Experimental Cancer Research, Semmelweis University, H-1085 Budapest, Hungary.ORCID 0000-0002-0179-3378
Dávid PappMTA-ELTE Lendület Ion Mobility Mass Spectrometry Research Group, ELTE Eötvös Loránd University, H-1117 Budapest, Hungary.
Gitta SchlosserMTA-ELTE Lendület Ion Mobility Mass Spectrometry Research Group, ELTE Eötvös Loránd University, H-1117 Budapest, Hungary.ORCID 0000-0002-7637-7133
Csaba TóthTeaching Hospital Markusovszky, University of Pécs, H-9700 Szombathely, Hungary.
Tamás TornóczkyDepartment of Pathology, Faculty of Medicine and Clinical Center, University of Pécs, H-7624 Pécs, Hungary.
László DrahosMS Proteomics Research Group, Research Centre for Natural Sciences, H-1117 Budapest, Hungary.ORCID 0000-0001-9589-6652
Lilla TuriákMS Proteomics Research Group, Research Centre for Natural Sciences, H-1117 Budapest, Hungary.ORCID 0000-0002-2139-8156
HUN-REN Research Centre for Natural Sciences · HUSemmelweis University · HUEötvös Loránd University · HUBudapest University of Technology and Economics · HUMarkusovszky Egyetemi Oktatókórház · HUUniversity of Pecs · HU

Funding

Hungarian Academy of Sciences János Bolyai Research Scholarship, KGYNK 2022-23Hungarian Academy of Sciences Lendület (Momentum) ProgramHungarian Ministry for Innovation and Technology ELTE Thematic Excellence ProgrammeNational Research, Development, and Innovation Fund, Hungary 2018-1.2.1-NKP-2018-00005, FK 131603, SNN 138407
6 · The paper itself

Abstract

Lung cancer is one of the most commonly diagnosed cancer types. Studying the molecular changes that occur in lung cancer is important to understand tumor formation and identify new therapeutic targets and early markers of the disease to decrease mortality. Glycosaminoglycan chains play important roles in various signaling events in the tumor microenvironment. Therefore, we have determined the quantity and sulfation characteristics of chondroitin sulfate and heparan sulfate in formalin-fixed paraffin-embedded human lung tissue samples belonging to different lung cancer types as well as tumor adjacent normal areas. Glycosaminoglycan disaccharide analysis was performed using HPLC-MS following on-surface lyase digestion. Significant changes were identified predominantly in the case of chondroitin sulfate; for example, the total amount was higher in tumor tissue compared to the adjacent normal tissue. We also observed differences in the degree of sulfation and relative proportions of individual chondroitin sulfate disaccharides between lung cancer types and adjacent normal tissue. Furthermore, the differences in the 6-

Indexed as

GlycosaminoglycansLung NeoplasmsChondroitin SulfatesDisaccharidesHeparan SulfateHumansPilot ProjectsTumor MicroenvironmentChondroitin SulfatesDisaccharidesGlycosaminoglycansHeparan Sulfateadenocarcinomachondroitin sulfateglycosaminoglycanheparan sulfateHPLClarge cell carcinomalung cancermass spectrometrysmall cell carcinomasquamous cell carcinoma

Identifiers

PMID37108213
PMCPMC10138872
OpenAlexW4365147397

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.