Evidence map›Paper›PMID 30212533›Full record

ArticlePloS one2018

Ex vivo drug sensitivity testing as a means for drug repurposing in esophageal adenocarcinoma.

Ines Lohse, Hassan Al-Ali, Claude-Henry Volmar, Annamil D Alvarez Trotta, Shaun P Brothers, Anthony J Capobianco, Claes Wahlestedt

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. 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
0.4field-weighted citation impact, top 39% 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, 8 citations in OpenAlex.

  1. Drug Sensitivity Testing in Osteosarcoma: A Case Report.Current oncology (Toronto, Ont.) · 2025
    Article
  2. Article
  3. Review
  4. Recycling the Purpose of Old Drugs to Treat Ovarian Cancer.International journal of molecular sciences · 2020
    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 1 institution in 1 country.

Ines LohseCenter for Therapeutic Innovation, Miller School of Medicine, University of Miami, Miami, Florida, United States of America.
Hassan Al-AliSylvester Comprehensive Cancer Center, University of Miami, Miami, Florida, United States of America.
Claude-Henry VolmarCenter for Therapeutic Innovation, Miller School of Medicine, University of Miami, Miami, Florida, United States of America.ORCID 0000-0001-9437-051X
Annamil D Alvarez TrottaSylvester Comprehensive Cancer Center, University of Miami, Miami, Florida, United States of America.
Shaun P BrothersCenter for Therapeutic Innovation, Miller School of Medicine, University of Miami, Miami, Florida, United States of America.
Anthony J CapobiancoSylvester Comprehensive Cancer Center, University of Miami, Miami, Florida, United States of America.
Claes WahlestedtCenter for Therapeutic Innovation, Miller School of Medicine, University of Miami, Miami, Florida, United States of America.ORCID 0000-0003-4471-5916
University of Miami · US

Funding

Development of Nociceptin Receptor Agonists for Post-Traumatic Stress DisorderR01MH110441 · NIMH · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI BROTHERS, SHAUN P · 2016 to 2019
$3.0M
Epigenetic Signaling Pathways Contributing to Alcohol DependenceR01AA023781 · NIAAA · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI HEILIG, MARKUS ALEXANDER, WAHLESTEDT, CLAES ROBERT · 2015 to 2019
$2.1M
Small Molecule Identification for the Nociceptin Receptor to Treat Cocaine AbuseR01DA035055 · NIDA · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI WAHLESTEDT, CLAES ROBERT · 2012 to 2016
$1.7M
Upregulation of Iduronidase Enzyme in MPSI DiseaseR01NS092671 · NINDS · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI BROTHERS, SHAUN P · 2016 to 2020
$1.7M
Long noncoding RNAs and chromatin regulation in cocaine addictionR21DA035592 · NIDA · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI WAHLESTEDT, CLAES ROBERT · 2014 to 2015
$381k
NIAAA NIH HHS R01 AA023781NIDA NIH HHS R01 DA035055NIDA NIH HHS R21 DA035592NIMH NIH HHS R01 MH110441NINDS NIH HHS R01 NS092671
6 · The paper itself

Abstract

backgroundEsophageal cancer remains one of the hardest cancers to treat with rising incidence rates, low overall survival and high levels of treatment resistance. The lack of clinically available biomarkers hinder diagnosis and treatment stratification. While large scale sequencing approaches have uncovered a number of molecular makers, little has translated in the routine treatment of esophageal cancer patients. MATERIAL AND

methodsWe evaluate the treatment response towards a panel of 215 FDA-approved and 163 epigenetic compounds of 4 established and 2 patient-derived esophageal cancer cell lines. Cell viability was evaluated after 72h of treatment using cell titer glow. The drug sensitivity testing results for gemcitabine and cisplatin were validated using clonogenic assays.

resultsThe tested cell lines display different drug sensitivity profiles, although we found compounds that display efficacy in all of the tested established or patient-derived cell lines. Clonogenic assays confirmed the validity of the drug sensitivity testing results. Using the epigenetic library, we observed high sensitivity towards a number of epigenetic modifiers. DISCUSSION: Ex vivo drug sensitivity testing may present a viable option for the treatment stratification of esophageal cancer patients and holds the potential to greatly improve patient outcome while reducing treatment toxicity.

Indexed as

AdenocarcinomaAntineoplastic AgentsCell Line, TumorCell SurvivalDrug Evaluation, PreclinicalDrug RepositioningEsophageal NeoplasmsHumansAntineoplastic Agents

Identifiers

PMID30212533
PMCPMC6136712
OpenAlexW2890241566

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.