Evidence map›Paper›PMID 27250034›Full record

ArticleOncotarget2016

Prognostic relevance of autophagy markers LC3B and p62 in esophageal adenocarcinomas.

Olivia Adams, Bastian Dislich, Sabina Berezowska, Anna M Schläfli, Christian A Seiler, Dino Kröll, Mario P Tschan, Rupert Langer

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

35 citing papers in PubMed, 56 citations in OpenAlex.

  1. The Roles of SQSTM1/p62 in Selective Autophagy and Oncogenic Signaling.International journal of molecular sciences · 2026
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  12. Frontiers in pharmacology · 2022
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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 1 institution in 1 country.

Olivia AdamsInstitute of Pathology, University of Bern, Bern, Switzerland.
Bastian DislichInstitute of Pathology, University of Bern, Bern, Switzerland.
Sabina BerezowskaInstitute of Pathology, University of Bern, Bern, Switzerland.
Anna M SchläfliInstitute of Pathology, University of Bern, Bern, Switzerland.
Christian A SeilerDepartment of Visceral Surgery and Medicine, Inselspital University Hospital Bern and University of Bern, Bern, Switzerland.
Dino KröllDepartment of Visceral Surgery and Medicine, Inselspital University Hospital Bern and University of Bern, Bern, Switzerland.
Mario P TschanInstitute of Pathology, University of Bern, Bern, Switzerland.
Rupert LangerInstitute of Pathology, University of Bern, Bern, Switzerland.
University of Bern · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Esophageal adenocarcinomas (EAC) are aggressive tumors with considerable rates of chemoresistance. Autophagy is a lysosome-dependent degradation process, characterized by the formation of vesicles called autophagosomes, and has been implicated in cancer. Protein light chain 3 B (LC3B) and p62 are associated with autophagosomal membranes and degraded. We aimed to assess the impact of basal autophagy on EAC. In EAC cell lines, an increase in LC3B and p62 was observed with increasing concentrations of the autophagy inhibitor chloroquine, which indicates functional basal autophagy. LC3B and p62 immunohistochemistry was performed on primary resected EAC. High LC3B and p62 expression was associated with earlier tumor stages (p < 0.05). High nuclear and cytoplasmic p62 staining were associated with a better prognosis (p = 0.006; p = 0.028). Various combinations of p62 expression with or without LC3B expression identified different prognostic groups. Tumors with low total p62 (p = 0.007) or low LC3B/low p62 expression had the worst outcome (p = 0.007; p = 0.005). A combination score of dot-like/cytoplasmic p62 and nuclear p62 staining was an independent prognostic parameter (p = 0.033; HR = 0.6). This study highlights the potential significance of basal autophagy in EAC biology. Tumors with low LC3B and p62 expression show the most aggressive behavior and may be candidates for autophagy regulating therapeutics.

Indexed as

AutophagyAdenocarcinomaAdultAgedAged, 80 and overBiomarkers, TumorEsophageal NeoplasmsFemaleHumansLysosomesMaleMicrotubule-Associated ProteinsMiddle AgedPrognosisRNA-Binding ProteinsTreatment OutcomeBiomarkers, TumorMAP1LC3B protein, humanMicrotubule-Associated ProteinsP62 protein, humanRNA-Binding Proteinsautophagyesophageal adenocarcinomaLC3Bp62Pathology Section

Identifiers

PMID27250034
PMCPMC5129929
OpenAlexW2405960299

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.