Evidence map›Paper›PMID 26504856›Full record

ArticleJournal of immunology research2015

Liver Expression of Sulphotransferase 2A1 Enzyme Is Impaired in Patients with Primary Sclerosing Cholangitis: Lack of the Response to Enhanced Expression of PXR.

Ewa Wunsch, Marta Klak, Urszula Wasik, Malgorzata Milkiewicz, Malgorzata Blatkiewicz, Elzbieta Urasinska, Olivier Barbier, Dariusz Bielicki, Dimitrios P Bogdanos, Elwyn Elias and 1 more

Open access · goldAbstract read
In one paragraph

Article in Journal of immunology research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

14 citing papers in PubMed, 22 citations in OpenAlex.

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  9. The Role of Sulfotransferases in Liver Diseases.Drug metabolism and disposition: the biological fate of chemicals · 2020
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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

11 authors at 5 institutions in 4 countries.

Ewa WunschDepartment of Clinical and Molecular Biochemistry, Pomeranian Medical University, 70-111 Szczecin, Poland.
Marta KlakDepartment of Medical Biology, Pomeranian Medical University, 70-111 Szczecin, Poland.
Urszula WasikDepartment of Medical Biology, Pomeranian Medical University, 70-111 Szczecin, Poland.
Malgorzata MilkiewiczDepartment of Medical Biology, Pomeranian Medical University, 70-111 Szczecin, Poland.
Malgorzata BlatkiewiczDepartment of Medical Biology, Pomeranian Medical University, 70-111 Szczecin, Poland.
Elzbieta UrasinskaDepartment of Pathology, Pomeranian Medical University, 71-252 Szczecin, Poland.
Olivier BarbierLaboratory of Molecular Pharmacology, CHU Québec and Faculty of Pharmacy, Laval University, Québec, QC, Canada.
Dariusz BielickiDepartment of Gastroenterology, Pomeranian Medical University, 71-252 Szczecin, Poland.
Dimitrios P BogdanosLiver Sciences, Division of Liver Transplantation and Mucosal Biology, King's College London School of Medicine, Denmark Hill Campus, London SE5 9RS, UK ; Faculty of Medicine, School of Health Sciences, University of Thessaly, Larissa 41110, Greece.
Elwyn EliasLiver and Hepatobiliary Unit, Queen Elizabeth Hospital, University of Birmingham, Birmingham B15 2TT, UK.
Piotr MilkiewiczDepartment of Clinical and Molecular Biochemistry, Pomeranian Medical University, 70-111 Szczecin, Poland ; Liver and Internal Medicine Unit, Department of General, Transplant and Liver Surgery, Medical University of Warsaw, 02-097 Warsaw, Poland.
Pomeranian Medical University · PLMedical University of Warsaw · PLQueen Elizabeth Hospital Birmingham · GBUniversité Laval · CAUniversity of Thessaly · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimSulphotransferase 2A1 (SULT2A1) exerts hepatoprotective effects. Transcription of SULT2A1 gene is induced by pregnane-X-receptor (PXR) and can be repressed by miR-378a-5p. We studied the PXR/SULT2A1 axis in chronic cholestatic conditions: primary sclerosing cholangitis (PSC) and primary biliary cirrhosis (PBC). MATERIALS/

methodsWestern-blot/PCRs for SULT2A1/PXR were performed in PSC (n = 11), PBC (n = 19), and control liver tissues (n = 19). PXR and SULT2A1 mRNA was analyzed in intestinal tissues from 22 PSC patients. Genomic DNA was isolated from blood of PSC patients (n = 120) and an equal number of healthy volunteers. Liver miRNA expression was evaluated using Affymetrix-Gene-Chip miRNA4.0.

resultsIncreased PXR protein was observed in both PSC and PBC compared to controls and was accompanied by a significant increase of SULT2A1 in PBC but not in PSC. Decreased expression of SULT2A1 mRNA was also seen in ileum of patients with PSC. Unlike PBC, miRNA analysis in PSC has shown a substantial increase in liver miR-378a-5p.

conclusionsPSC is characterized by disease-specific impairment of SULT2A1 expression following PXR activation, a phenomenon which is not noted in PBC, and may account for the impaired hepatoprotection in PSC. miRNA analysis suggests that SULT2A1 expression in PSC may be regulated by miR-378a-5p, connoting its pathogenic role.

Indexed as

AdolescentAdultAgedBase SequenceCholangitis, SclerosingFemaleGene Expression RegulationHumansIntestine, SmallLiverLiver Cirrhosis, BiliaryMaleMicroRNAsMiddle AgedMolecular Sequence DataPolymorphism, Single Nucleotidealcohol sulfotransferaseMicroRNAsMIRN378 microRNA, humanPregnane X ReceptorReceptors, SteroidRNA, MessengerSulfotransferases

Identifiers

PMID26504856
PMCPMC4609469
OpenAlexW1931624384

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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.