Evidence map›Paper›PMID 37755493›Full record

ArticleJournal of molecular medicine (Berlin, Germany)2023

Microdevices for cancer stem cell culture as a predictive chemotherapeutic response platform.

Eduardo Imanol Agüero, Denise Belgorosky, Julio Israel García-Silva, Ross Booth, Betiana Lerner, Maximiliano Sebastián Pérez, Ana María Eiján

Erratum issuedAbstract read
PubMed Publisher
In one paragraph

Article in Journal of molecular medicine (Berlin, Germany), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 42% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 3 countries.

Eduardo Imanol AgüeroFacultad de Ciencias Médicas, Instituto de Oncología "Ángel H. Roffo", Área de Investigación, Universidad de Buenos Aires, C1417DTB, Ciudad Autónoma de Buenos Aires, Argentina.
Denise BelgoroskyFacultad de Ciencias Médicas, Instituto de Oncología "Ángel H. Roffo", Área de Investigación, Universidad de Buenos Aires, C1417DTB, Ciudad Autónoma de Buenos Aires, Argentina.
Julio Israel García-SilvaConsejo Nacional de Investigaciones Científicas y Técnicas (CONICET), C1425FQB, Ciudad Autónoma de Buenos Aires, Argentina.
Ross BoothRoche Sequencing Solutions, Santa Clara, CA, 95050, USA.
Betiana LernerDepartment of Electrical and Computer Engineering, Florida International University (FIU), Miami, FL, 33174, USA.
Maximiliano Sebastián PérezDepartment of Electrical and Computer Engineering, Florida International University (FIU), Miami, FL, 33174, USA. maxperez@fiu.edu.
Ana María EijánFacultad de Ciencias Médicas, Instituto de Oncología "Ángel H. Roffo", Área de Investigación, Universidad de Buenos Aires, C1417DTB, Ciudad Autónoma de Buenos Aires, Argentina. anamariaeijan@gmail.com.ORCID 0000-0002-2723-0194
Consejo Nacional de Investigaciones Científicas y Técnicas · ARNational Technological University · ARUniversidad de Buenos Aires · AR

Funding

Agencia Nacional de Promoción Científica y Tecnológica PICT-2017-0776Agencia Nacional de Promoción Científica y Tecnológica PICT 2018-02804Agencia Nacional de Promoción de la Investigación, el Desarrollo Tecnológico y la Innovación PICT START-UP-2020-00017Consejo Nacional de Investigaciones Científicas y Técnicas PIP9671/14Secretaria de Ciencia y Tecnica, Universidad de Buenos Aires 20720190100005BA
6 · The paper itself

Abstract

Microfluidic platforms for clinical use are a promising translational strategy for cancer research specially for drug screening. Identifying cancer stem cells (CSC) using sphere culture techniques in microfluidic devices (MDs) showed to be better reproducing physiological responses than other in vitro models and allow the optimization of samples and reagents. We evaluated individual sphere proliferation and stemness toward chemotherapeutic treatment (CT) with doxorubicin and cisplatin in bladder cancer cell lines (MB49-I and J82) cultured in MDs used as CSC treatment response platform. Our results confirm the usefulness of this device to evaluate the CT effect in sphere-forming efficiency, size, and growth rate from individual spheres within MDs and robust information comparable to conventional culture plates was obtained. The expression of pluripotency genetic markers (Oct4, Sox2, Nanog, and CD44) could be analyzed by qPCR and immunofluorescence in spheres growing directly in MDs. MDs are a suitable platform for sphere isolation from tumor samples and can provide information about CT response. Microfluidic-based CSC studies could provide information about treatment response of cancer patients from small samples and can be a promising tool for CSC-targeted specific treatment with potential in precision medicine. KEY MESSAGES: We have designed a microfluidic platform for CSC enriched culture by tumor sphere formation. Using MDs, we could quantify and determine sphere response after CT using murine and human cell lines as a proof of concept. MDs can be used as a tumor-derived sphere isolation platform to test the effect of antitumoral compounds in sphere proliferation.

Indexed as

Drug Delivery SystemsNeoplasmsAnimalsCell Line, TumorHumansMiceNeoplastic Stem CellsBladder cancerCancer stem cellsChemotherapeutic treatmentLab-on-a-chipMicrofluidic devices

Identifiers

PMID37755493
OpenAlexW4387078305

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.