Evidence map›Paper›PMID 33377455›Full record

ArticleInternational journal of stem cells2021

Human Stem Cell-Derived Retinal Pigment Epithelial Cells as a Model for Drug Screening and Pre-Clinical Assays Compared to ARPE-19 Cell Line.

Carolina Reis Oliveira, Mayara Rodrigues Brandão de Paiva, Marcela Coelho Silva Ribeiro, Gracielle Ferreira Andrade, Juliana Lott Carvalho, Dawidson Assis Gomes, Márcio Nehemy, Sílvia Ligório Fialho, Armando Silva-Cunha, Alfredo Miranda de Góes

Open access · diamondAbstract read
In one paragraph

Article in International journal of stem cells, 2021. 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
0.2field-weighted citation impact, top 48% 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, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Looking for In Vitro Models for Retinal Diseases.International journal of molecular sciences · 2021
    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 3 institutions in 1 country.

Carolina Reis Oliveira1Department of Biochemistry and Immunology, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Mayara Rodrigues Brandão de PaivaFaculty of Pharmacy, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Marcela Coelho Silva RibeiroFaculty of Pharmacy, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Gracielle Ferreira AndradeSENAN, Centro de Desenvolvimento da Tecnologia Nuclear - CDTN/CNEN, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Juliana Lott CarvalhoDepartment of Genomic Sciences and Biotechnology, Catholic University of Brasília, Brasília, Brazil.
Dawidson Assis Gomes1Department of Biochemistry and Immunology, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Márcio NehemyDepartment of Ophthalmology, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Sílvia Ligório FialhoPharmaceutical Research and Development, Ezequiel Dias Foundation, Belo Horizonte, Brazil.
Armando Silva-CunhaFaculty of Pharmacy, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Alfredo Miranda de Góes1Department of Biochemistry and Immunology, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Universidade Federal de Minas Gerais · BREzequiel Dias Foundation · BRUniversidade Católica de Brasília · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesEye diseases have a high socioeconomic impact on society and may be one of the fields in which most stem cell-related scientific accomplishments have been achieved recently. In this context, human Pluripotent Stem Cell (hPSC) technology arises as an important tool to produce and study human Embryonic Stem cell derived-Retinal Pigmented Epithelial Cells (hES-RPE) for several applications, such as cell therapy, disease modeling, and drug screening. The use of this technology in pre-clinical phases attends to the overall population desire for animal-free product development. Here, we aimed to compare hES-RPE cells with ARPE-19, one of the most commonly used retinal pigmented epithelial immortalized cell lines. METHODS AND

resultsFunctional, cellular and molecular data obtained suggest that hES-RPE cells more closely resembles native RPEs compared to ARPE-19. Furthermore, hES-RPE revealed an interesting robustness when cultured on human Bruch's membrane explants and after exposure to Cyclosporine (CSA), Sirolimus (SRL), Tacrolimus (TAC), Leflunomide (LEF) and Teriflunomide (TER). On these conditions, hES-RPE cells were able to survive at higher drug concentrations, while ARPE-19 cell line was more susceptible to cell death.

conclusionsTherefore, hES-RPEs seem to have the ability to incur a broader range of RPE functions than ARPE-19 and should be more thoroughly explored for drug screening.

Indexed as

ARPE-19Human embryonic stem cell derived-retinal pigmented epithelial cellsIn vitro modelIn vitro toxicology

Identifiers

PMID33377455
PMCPMC7904525
OpenAlexW3113457799

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.