Evidence map›Paper›PMID 37878028›Full record

ArticleJournal of molecular medicine (Berlin, Germany)2024

Autophagy and nuclear morphometry are associated with histopathologic features in esophageal squamous cell carcinoma.

Ricardo Iserhard, Emily Ferreira Salles Pilar, Francine Hehn de Oliveira, Sidia Maria Callegari-Jacques, Paula Ferst, Fernanda Visioli, Antonio Barros Lopes, Patrícia Luciana da Costa Lopez, Eduardo Cremonese Filippi-Chiela

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of molecular medicine (Berlin, Germany), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 32% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
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

9 authors at 2 institutions in 1 country.

Ricardo IserhardGraduate Program in Gastroenterology and Hepatology, Faculty of Medical Sciences, Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre, Rio Grande do Sul, Brazil.
Emily Ferreira Salles PilarHospital de Clínicas de Porto Alegre, Porto Alegre, Rio Grande do Sul, Brazil.
Francine Hehn de OliveiraHospital de Clínicas de Porto Alegre, Porto Alegre, Rio Grande do Sul, Brazil.
Sidia Maria Callegari-JacquesDepartment of Genetics, UFRGS, Porto Alegre, Rio Grande do Sul, Brazil.
Paula FerstHospital de Clínicas de Porto Alegre, Porto Alegre, Rio Grande do Sul, Brazil.
Fernanda VisioliHospital de Clínicas de Porto Alegre, Porto Alegre, Rio Grande do Sul, Brazil.
Antonio Barros LopesGraduate Program in Gastroenterology and Hepatology, Faculty of Medical Sciences, Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre, Rio Grande do Sul, Brazil.
Patrícia Luciana da Costa LopezGraduate Program in Gastroenterology and Hepatology, Faculty of Medical Sciences, Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre, Rio Grande do Sul, Brazil.
Eduardo Cremonese Filippi-ChielaGraduate Program in Gastroenterology and Hepatology, Faculty of Medical Sciences, Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre, Rio Grande do Sul, Brazil. echiela@hcpa.edu.br.ORCID 0000-0001-8192-3779
Universidade Federal do Rio Grande do Sul · BRHospital de Clínicas de Porto Alegre · BR

Funding

Fundação de Apoio ao Ensino, Pesquisa e Assistência do Hospital das Clínicas da Faculdade de Medicina de Ribeirão Preto da Universidade de São Paulo 16-0233
6 · The paper itself

Abstract

Less than 15% of patients with esophageal squamous cell carcinoma (ESCC) survive 5 years after diagnosis. A better understanding of the biology of these tumors and the development of clinical biomarkers is needed. Autophagy is a physiological mechanism involved in the turnover of cellular components that plays a key role in cancer. This study evaluated the differential levels of three key regulators of autophagy (SQSTM1, MAP1LC3B, and BECN1) in patients with ESCC, associating autophagy with histopathologic features, including the grade of differentiation, mitotic rate, inflammation score, and the intensity of tumor-infiltrating lymphocytes. Nuclear morphometry of the tumor parenchyma was also assessed, associating it with autophagy and histopathology. All three markers significantly increased in patients with ESCC compared to the control group. Based on the mean expression of each protein in the control group, 57% of patients with ESCC had high levels of all three markers compared to control patients (14%). The most frequent profiles found in ESCC were BECN

Indexed as

Carcinoma, Squamous CellEsophageal NeoplasmsEsophageal Squamous Cell CarcinomaAutophagyBiomarkers, TumorHumansSequestosome-1 ProteinBiomarkers, TumorSequestosome-1 ProteinAutophagyEsophageal squamous cell carcinoma (ESCC)HistopathologyNuclear morphometryPrognosis

Identifiers

PMID37878028
OpenAlexW4387931606

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.