Evidence map›Paper›PMID 37686684›Full record

ArticleCancers2023

High-Throughput Drug Screening Revealed That Ciclopirox Olamine Can Engender Gastric Cancer Stem-like Cells.

Diana Pádua, Paula Figueira, Mariana Pinto, André Filipe Maia, Joana Peixoto, Raquel T Lima, António Pombinho, Carlos Filipe Pereira, Raquel Almeida, Patrícia Mesquita

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2023. 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
0.6field-weighted citation impact, top 30% 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, 4 citations in OpenAlex.

  1. Ciclopirox Olamine Inhibits the NLRP3 Inflammasome to Alleviate Inflammatory Diseases.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  2. Article
  3. Article
  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

10 authors at 2 institutions in 2 countries.

Diana Páduai3S-Institute for Research and Innovation in Health, University of Porto, 4200-135 Porto, Portugal.ORCID 0000-0002-5780-9842
Paula Figueirai3S-Institute for Research and Innovation in Health, University of Porto, 4200-135 Porto, Portugal.
Mariana Pintoi3S-Institute for Research and Innovation in Health, University of Porto, 4200-135 Porto, Portugal.ORCID 0009-0000-9179-291X
André Filipe Maiai3S-Institute for Research and Innovation in Health, University of Porto, 4200-135 Porto, Portugal.ORCID 0000-0001-5987-7016
Joana Peixotoi3S-Institute for Research and Innovation in Health, University of Porto, 4200-135 Porto, Portugal.ORCID 0000-0001-9469-5680
Raquel T Limai3S-Institute for Research and Innovation in Health, University of Porto, 4200-135 Porto, Portugal.ORCID 0000-0002-5838-9659
António Pombinhoi3S-Institute for Research and Innovation in Health, University of Porto, 4200-135 Porto, Portugal.
Carlos Filipe PereiraCNC-Center for Neuroscience and Cell Biology, University of Coimbra, 3004-517 Coimbra, Portugal.ORCID 0000-0002-9724-1382
Raquel Almeidai3S-Institute for Research and Innovation in Health, University of Porto, 4200-135 Porto, Portugal.
Patrícia Mesquitai3S-Institute for Research and Innovation in Health, University of Porto, 4200-135 Porto, Portugal.ORCID 0000-0002-4766-9831
Universidade do Porto · PTLund University · SE

Funding

Fundação para a Ciência e a Tecnologia (FCT), co-sponsored by Fundo Social Europeu (FSE) through North Portugal Regional Operational Programme SFRH/BD/146186/2019Norte Portugal Regional Operational Programme (NORTE 2020), under the PORTUGAL 2020 Partnership Agreement, through the European Regional Development Fund (FEDER) Norte-01-0145-FEDER-000051Programa Operacional Regional do Norte and European Regional Development Fund under the project "The Porto Comprehensive Cancer Center" - Consórcio PORTO.CCC. NORTE-01-0145-FEDER-072678
6 · The paper itself

Abstract

Cancer stem cells (CSCs) are relevant therapeutic targets for cancer treatment. Still, the molecular circuits behind CSC characteristics are not fully understood. The low number of CSCs can sometimes be an obstacle to carrying out assays that explore their properties. Thus, increasing CSC numbers via small molecule-mediated cellular reprogramming appears to be a valid alternative tool. Using the SORE6-GFP reporter system embedded in gastric non-CSCs (SORE6-), we performed a high-throughput image-based drug screen with 1200 small molecules to identify compounds capable of converting SORE6- to SORE6+ (CSCs). Here, we report that the antifungal agent ciclopirox olamine (CPX), a potential candidate for drug repurposing in cancer treatment, is able to reprogram gastric non-CSCs into cancer stem-like cells via activation of SOX2 expression and increased expression of C-MYC, HIF-1α, KLF4, and HMGA1. This reprogramming depends on the CPX concentration and treatment duration. CPX can also induce cellular senescence and the metabolic shift from oxidative phosphorylation (OXPHOS) to glycolysis. We also disclose that the mechanism underlying the cellular reprogramming is similar to that of cobalt chloride (CoCl

Indexed as

cancer stem cellscellular reprogrammingcellular senescenceciclopiroxcobalt chloridegastric cancermetabolic reprogrammingtranscription factors

Identifiers

PMID37686684
PMCPMC10487151
OpenAlexW4386417738

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.