Evidence map›Paper›PMID 26259963›Full record

ArticleVirchows Archiv : an international journal of pathology2015

In recurrent primary biliary cirrhosis after liver transplantation, biliary epithelial cells show increased expression of mitochondrial proteins.

Motoko Sasaki, Maylee Hsu, Matthew M Yeh, Yasuni Nakanuma

Abstract read
PubMed Publisher
In one paragraph

Article in Virchows Archiv : an international journal of pathology, 2015. 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
1.0field-weighted citation impact, top 26% 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, 13 citations in OpenAlex.

  1. Article
  2. Article
  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

4 authors at 3 institutions in 2 countries.

Motoko SasakiDepartment of Human Pathology, Kanazawa University Graduate School of Medicine, Kanazawa, 920-8640, Japan. m8sasaki@med.kanazawa-u.ac.jp.
Maylee HsuDepartment of Pathology, University of Washington, Seattle, WA, 98195, USA.
Matthew M YehDepartment of Pathology, University of Washington, Seattle, WA, 98195, USA.
Yasuni NakanumaDepartment of Human Pathology, Kanazawa University Graduate School of Medicine, Kanazawa, 920-8640, Japan.
University of Washington · USKanazawa University · JPShizuoka Cancer Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In biliary epithelial lesions in primary biliary cirrhosis (PBC), mitochondrial proteins associated with deregulated autophagy are abnormally expressed. We examined whether this could be used as a diagnostic marker for end-stage PBC and recurrent PBC after liver transplantation. We examined the expression of the mitochondrial protein pyruvate dehydrogenase complex-E2 component and cytochrome c oxidase, subunit I (CCO), the autophagy-related marker microtubule-associated protein-light chain 3 (LC3), and p62/sequestosome-1 and the senescence markers p16(Ink4a) and p21(WAF1/Cip1) in small bile ducts and bile ductules in explanted livers from patients with PBC (n = 20) in comparison with liver tissue from control patients (n = 21) and post-transplant samples including recurrent PBC and cellular rejection (n = 28). Intense granular expression of mitochondrial proteins was significantly more frequent in small bile ducts in explanted livers with PBC than in control livers (p < 0.05). Post-transplant samples comprised of three groups: group A (positive for mitochondrial proteins, n = 7), group B (positive for either autophagy-related or senescence markers but negative for mitochondrial proteins, n = 7), and group C (all negative, n = 14). All but one case of group A were clinically and histologically diagnosed as recurrent PBC. In contrast, all cases of group B were diagnosed as cellular rejection. This study suggests that the expression of mitochondrial proteins in small bile ducts may be a useful diagnostic marker for end-stage PBC and recurrent PBC after liver transplantation.

Indexed as

Alanine TransaminaseAutophagyBile DuctsBiomarkersCyclin-Dependent Kinase Inhibitor p16Dihydrolipoyllysine-Residue AcetyltransferaseElectron Transport Complex IVEpithelial CellsHumansLiver Cirrhosis, BiliaryLiver TransplantationMitochondrial ProteinsNeoplasm ProteinsRecurrenceRNA-Binding ProteinsAlanine TransaminaseBiomarkersCDKN2A protein, humanCyclin-Dependent Kinase Inhibitor p16cytochrome c oxidase subunit I, humanDihydrolipoyllysine-Residue AcetyltransferaseElectron Transport Complex IVMitochondrial ProteinsNeoplasm ProteinsP62 protein, humanRNA-Binding ProteinsAutophagy and cellular senescenceBiliary epithelial cellPost-liver transplant rejectionPrimary biliary cirrhosisPyruvate dehydrogenase complex-E2 component

Identifiers

PMID26259963
OpenAlexW1161903148

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.