Evidence map›Paper›PMID 35344068›Full record

ArticleAnalytical and bioanalytical chemistry2022

Expression of glycosaminoglycans in cirrhotic liver and hepatocellular carcinoma-a pilot study including etiology.

Gábor Tóth, Domonkos Pál, Simon Sugár, Ilona Kovalszky, Katalin Dezső, Gitta Schlosser, László Drahos, Lilla Turiák

Open access · hybridAbstract read
In one paragraph

Article in Analytical and bioanalytical chemistry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.4field-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

9 citing papers in PubMed, 14 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

8 authors at 4 institutions in 1 country.

Gábor TóthMS Proteomics Research Group, Research Centre for Natural Sciences, Magyar tudósok körútja 2, H-1117, Budapest, Hungary.ORCID http://orcid.org/0000-0003-1428-7906
Domonkos PálMS Proteomics Research Group, Research Centre for Natural Sciences, Magyar tudósok körútja 2, H-1117, Budapest, Hungary.ORCID http://orcid.org/0000-0002-0226-0004
Simon SugárMS Proteomics Research Group, Research Centre for Natural Sciences, Magyar tudósok körútja 2, H-1117, Budapest, Hungary.ORCID http://orcid.org/0000-0001-9728-5732
Ilona Kovalszky1st Department of Pathology and Experimental Cancer Research, Semmelweis University, Üllői út 26, 1085, Budapest, Hungary.ORCID http://orcid.org/0000-0002-0179-3378
Katalin Dezső1st Department of Pathology and Experimental Cancer Research, Semmelweis University, Üllői út 26, 1085, Budapest, Hungary.ORCID http://orcid.org/0000-0002-4856-0483
Gitta SchlosserMTA-ELTE Lendület Ion Mobility Mass Spectrometry Research Group, Eötvös Loránd University, Pázmány Péter sétány 1, 1117, Budapest, Hungary.ORCID http://orcid.org/0000-0002-7637-7133
László DrahosMS Proteomics Research Group, Research Centre for Natural Sciences, Magyar tudósok körútja 2, H-1117, Budapest, Hungary.ORCID http://orcid.org/0000-0001-9589-6652
Lilla TuriákMS Proteomics Research Group, Research Centre for Natural Sciences, Magyar tudósok körútja 2, H-1117, Budapest, Hungary. turiak.lilla@ttk.hu.ORCID http://orcid.org/0000-0002-2139-8156
HUN-REN Research Centre for Natural Sciences · HUSemmelweis University · HUBudapest University of Technology and Economics · HUEötvös Loránd University · HU

Funding

Hungarian National Excellence program NTP-NFTÖ-20-B-0203Magyar Tudományos Akadémia János Bolyai Research ScholarshipNemzeti Kutatási Fejlesztési és Innovációs Hivatal 2018-1.2.1-NKP-2018-00005Nemzeti Kutatási Fejlesztési és Innovációs Hivatal FK 131603Nemzeti Kutatási Fejlesztési és Innovációs Hivatal FK 138673Nemzeti Kutatási Fejlesztési és Innovációs Hivatal K 119283Nemzeti Kutatási Fejlesztési és Innovációs Hivatal PD 121187
6 · The paper itself

Abstract

Chronic liver diseases have both high incidence and mortality rates; therefore, a deeper understanding of the underlying molecular mechanisms is essential. We have determined the content and sulfation pattern of chondroitin sulfate (CS) and heparan sulfate (HS) in human hepatocellular carcinoma and cirrhotic liver tissues, considering the etiology of the diseases. A variety of pathological conditions such as alcoholic liver disease, hepatitis B and C virus infections, and primary sclerosing cholangitis were studied. Major differences were observed in the total abundance and sulfation pattern of CS and HS chains. For example, the 6-O-sulfation of CS is fundamentally different regarding etiologies of cirrhosis, and a 2-threefold increase in HS N-sulfation/O-sulfation ratio was observed in hepatocellular carcinoma compared to cirrhotic tissues.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsChondroitin SulfatesGlycosaminoglycansHeparan SulfateHumansLiver CirrhosisPilot ProjectsChondroitin SulfatesGlycosaminoglycansHeparan SulfateChondroitin sulfateCirrhosisGlycosaminoglycanHeparan sulfateHepatocellular carcinomaLiver cancer

Identifiers

PMID35344068
PMCPMC8958808
OpenAlexW4221023168

What Socratic 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 Socratic graph.