Evidence map›Paper›PMID 27655834›Full record

ArticleCarcinogenesis2016

Prevention of DNA damage in Barrett's esophageal cells exposed to acidic bile salts.

Vikas Bhardwaj, Andela Horvat, Olga Korolkova, Mary K Washington, Wael El-Rifai, Sergey I Dikalov, Alexander I Zaika

Open access · bronzeAbstract read
In one paragraph

Article in Carcinogenesis, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Antioxidants (Basel, Switzerland) · 2023
    Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Gastroesophageal Reflux Induces Protein Adducts in the Esophagus.Cellular and molecular gastroenterology and hepatology · 2019
    Article
  12. Article
  13. 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

7 authors at 2 institutions in 1 country.

Vikas BhardwajDepartment of Veterans Affairs, Tennessee Valley Healthcare System, Nashville, TN 37212, USA.
Andela HorvatDepartment of Surgery.
Olga KorolkovaDepartment of Surgery.
Mary K WashingtonDepartment of Cancer Biology and.
Wael El-RifaiDepartment of Surgery.
Sergey I DikalovDivision of Clinical Pharmacology, Vanderbilt University Medical Center and Vanderbilt-Ingram Cancer Center, Nashville, TN 37232, USA.
Alexander I ZaikaDepartment of Veterans Affairs, Tennessee Valley Healthcare System, Nashville, TN 37212, USA, alex.zaika@vanderbilt.edu.
VA Tennessee Valley Healthcare System · USVanderbilt University Medical Center · US

Funding

Translational Analysis CoreP30DK058404 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RICHARD M. PEEK · 2002 to 2026
$29.9M
The Molecular Functions of APE1 in Barrett's TumorigenesisR01CA206563 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI EL-RIFAI, WAEL · 2015 to 2020
$2.2M
Mechanisms of Tumorigenic Transformation of Barretts EsophagusR01CA206564 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI ZAIKA, ALEXANDER I. · 2015 to 2019
$1.8M
Regulation of gastroesophageal reflux-associated tumorigenesisI01BX002115 · VA · VETERANS HEALTH ADMINISTRATION · PI ZAIKA, ALEXANDER I. · 2014 to 2024
–
BLRD Research Career Scientist Award ApplicationIK6BX003787 · VA · VETERANS HEALTH ADMINISTRATION · PI WAEL EL-RIFAI · 2017 to 2026
–
BLRD VA I01 BX002115BLRD VA IK6 BX003787NCI NIH HHS R01 CA206563NCI NIH HHS R01 CA206564NIDDK NIH HHS P30 DK058404
6 · The paper itself

Abstract

Esophageal adenocarcinoma (EA) is one of the fastest rising tumors in the USA. The major risk factor for EA is gastroesophageal reflux disease (GERD). During GERD, esophageal cells are exposed to refluxate which contains gastric acid frequently mixed with duodenal bile. This may lead to mucosal injury and Barrett's metaplasia (BE) that are important factors contributing to development of EA. In this study, we investigated DNA damage in BE cells exposed to acidic bile salts and explored for potential protective strategies. Exposure of BE cells to acidic bile salts led to significant DNA damage, which in turn, was due to generation of reactive oxygen species (ROS). We found that acidic bile salts induce a rapid increase in superoxide radicals and hydrogen peroxide, which were determined using electron paramagnetic resonance spectroscopy and Amplex Red assay. Analyzing a panel of natural antioxidants, we identified apocynin to be the most effective in protecting esophageal cells from DNA damage induced by acidic bile salts. Mechanistic analyses showed that apocynin inhibited ROS generation and increases the DNA repair capacity of BE cells. We identified BRCA1 and p73 proteins as apocynin targets. Downregulation of p73 inhibited the protective effect of apocynin. Taken together, our results suggest potential application of natural compounds such as apocynin for prevention of reflux-induced DNA damage and GERD-associated tumorigenesis.

Indexed as

AcetophenonesAcidsAdenocarcinomaAntioxidantsBarrett EsophagusBile Acids and SaltsBRCA1 ProteinCell Line, TumorDNA DamageDNA RepairEsophageal NeoplasmsGastric AcidGastroesophageal RefluxHumansReactive Oxygen SpeciesAcetophenonesacetovanilloneAcidsAntioxidantsBile Acids and SaltsBRCA1 ProteinBRCA1 protein, humanReactive Oxygen Species

Identifiers

PMID27655834
PMCPMC5137263
OpenAlexW2522192589

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.