Evidence map›Paper›PMID 40658268›Full record

ArticleHistochemistry and cell biology2025

Differentiation to insulin-positive cells from human amnion epithelial cells using a pancreatic development mimicry protocol.

Daniel Martínez-Rodríguez, Jonathan Salazar-Alonso, Axel Castro-Abrego, Daniela Ávila-González, Omar Martínez-Alarcón, Anayansi Molina-Hernández, Alejandro Martínez-Juárez, Héctor Salvador Godoy-Morales, Diana Elizabeth Lara-Barragán, Wendy Portillo and 3 more

Abstract read
In one paragraph

Article in Histochemistry and cell biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Review
  2. August in focus in HCB.Histochemistry and cell biology · 2025
    Article
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

13 authors.

Daniel Martínez-RodríguezDepartamento de Fisiología y Desarrollo Celular, Instituto Nacional de Perinatología Isidro Espinosa de Lo Reyes, Torre de Investigación 3Er Piso, Montes Urales 800, Colonia Lomas de Virreyes, Delegación Miguel Hidalgo, 11000, Mexico City, Mexico.
Jonathan Salazar-AlonsoDepartamento de Fisiología y Desarrollo Celular, Instituto Nacional de Perinatología Isidro Espinosa de Lo Reyes, Torre de Investigación 3Er Piso, Montes Urales 800, Colonia Lomas de Virreyes, Delegación Miguel Hidalgo, 11000, Mexico City, Mexico.
Axel Castro-AbregoDepartamento de Fisiología y Desarrollo Celular, Instituto Nacional de Perinatología Isidro Espinosa de Lo Reyes, Torre de Investigación 3Er Piso, Montes Urales 800, Colonia Lomas de Virreyes, Delegación Miguel Hidalgo, 11000, Mexico City, Mexico.
Daniela Ávila-GonzálezDepartamento de Fisiología y Desarrollo Celular, Instituto Nacional de Perinatología Isidro Espinosa de Lo Reyes, Torre de Investigación 3Er Piso, Montes Urales 800, Colonia Lomas de Virreyes, Delegación Miguel Hidalgo, 11000, Mexico City, Mexico.
Omar Martínez-AlarcónDepartamento de Fisiología y Desarrollo Celular, Instituto Nacional de Perinatología Isidro Espinosa de Lo Reyes, Torre de Investigación 3Er Piso, Montes Urales 800, Colonia Lomas de Virreyes, Delegación Miguel Hidalgo, 11000, Mexico City, Mexico.
Anayansi Molina-HernándezDepartamento de Fisiología y Desarrollo Celular, Instituto Nacional de Perinatología Isidro Espinosa de Lo Reyes, Torre de Investigación 3Er Piso, Montes Urales 800, Colonia Lomas de Virreyes, Delegación Miguel Hidalgo, 11000, Mexico City, Mexico.
Alejandro Martínez-JuárezDepartamento de Fisiología y Desarrollo Celular, Instituto Nacional de Perinatología Isidro Espinosa de Lo Reyes, Torre de Investigación 3Er Piso, Montes Urales 800, Colonia Lomas de Virreyes, Delegación Miguel Hidalgo, 11000, Mexico City, Mexico.
Héctor Salvador Godoy-MoralesUnidad de Medicina Reproductiva, Hospital Angeles Pedregal, 10700, Mexico City, Mexico.
Diana Elizabeth Lara-BarragánDepartamento de Ginecología y Obstetricia, Hospital Angeles Pedregal, 10700, Mexico City, Mexico.
Wendy PortilloInstituto de Neurobiologia, UNAM, 76230, Santiago de Queretaro, Mexico.
Nestor Emmanuel Díaz-MartínezLaboratorio de Reprogramación Celular y Bioingenería de Tejidos, Biotecnología Médica y Farmacéutica, Centro de Investigación y Asistencia en tecnología y Diseño del Estado de jalisoc (CIATEJ), Guadalajara, Jalisco, Mexico.
Guadalupe García-LópezDepartamento de Fisiología y Desarrollo Celular, Instituto Nacional de Perinatología Isidro Espinosa de Lo Reyes, Torre de Investigación 3Er Piso, Montes Urales 800, Colonia Lomas de Virreyes, Delegación Miguel Hidalgo, 11000, Mexico City, Mexico. guadalupegl2000@yahoo.com.mx.
Nestor Fabián DíazDepartamento de Fisiología y Desarrollo Celular, Instituto Nacional de Perinatología Isidro Espinosa de Lo Reyes, Torre de Investigación 3Er Piso, Montes Urales 800, Colonia Lomas de Virreyes, Delegación Miguel Hidalgo, 11000, Mexico City, Mexico. nfdiaz00@yahoo.com.mx.

Funding

Consejo Nacional de Humanidades, Ciencias y Tecnologías A1-S-8450Instituto Nacional de Perinatología 2019-1-40Instituto Nacional de Perinatología 21081Instituto Nacional de Perinatología,Mexico 2018-1-150
6 · The paper itself

Abstract

Diabetes mellitus (DM) is characterized by the loss or dysfunction pancreatic β-cells. Human amniotic epithelial cells (hAEC), which retain pluripotency markers and are readily obtainable from term placentas, represent a promising alternative source of stem cells. We investigated whether hAECs can be guided through pancreatic ontogeny to generate insulin-producing β-like cells. hAEC from uncomplicated term deliveries were expanded to passage 1 and exposed to a four-stage differentiation sequence that sequentially modulated Activin/WNT, KGF/TGF-β, retinoic-acid/hedgehog, and EGF/Noggin signaling. Stage progression was monitored by end-point RT-PCR and quantitative immunofluorescence for hallmark transcription factors. After definitive endoderm induction, 64% of cells were Brachyury positive and 71% were WNT3A positive; primitive-gut specification yielded 57% HNF1B

Indexed as

AmnionCell DifferentiationEpithelial CellsInsulinInsulin-Secreting CellsPancreasCells, CulturedFemaleHumansInsulinDifferentiationHuman amniotic epithelial cellsPancreatic beta cells

Identifiers

PMID40658268
PMCPMC12259741

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.