Evidence map›Paper›PMID 41489619›Full record

ReviewHuman reproduction update2026

Beyond integration: towards benchmarks for developmental potential in human stem cell-derived embryo models.

Dorian G Luijkx, Leila Ashtar, Nienke de Graeff, Edith Coonen, Stefan Giselbrecht, Guido M W R de Wert, Erik J Vrij, Rhiannon Grant, Ana M Pereira Daoud

Abstract readReview
In one paragraph

Review in Human reproduction update, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

9 authors.

Dorian G LuijkxDepartment for Cell Biology-Inspired Tissue Engineering, MERLN Institute for Technology-Inspired Regenerative Medicine, Maastricht University, Maastricht, The Netherlands.ORCID 0000-0001-8670-1470
Leila AshtarDepartment for Cell Biology-Inspired Tissue Engineering, MERLN Institute for Technology-Inspired Regenerative Medicine, Maastricht University, Maastricht, The Netherlands.ORCID 0009-0001-0513-8549
Nienke de GraeffDepartment of Medical Ethics and Health Law, Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0002-0045-4366
Edith CoonenDepartment of Clinical Genetics, Maastricht University Medical Center, Maastricht, The Netherlands.ORCID 0000-0002-8601-7369
Stefan GiselbrechtDepartment for Cell Biology-Inspired Tissue Engineering, MERLN Institute for Technology-Inspired Regenerative Medicine, Maastricht University, Maastricht, The Netherlands.ORCID 0000-0002-1354-0167
Guido M W R de WertDepartment of Obstetrics & Gynecology, GROW Research Institute for Oncology and Reproduction, Maastricht University, Maastricht, The Netherlands.ORCID 0000-0002-0410-4902
Erik J VrijDepartment for Cell Biology-Inspired Tissue Engineering, MERLN Institute for Technology-Inspired Regenerative Medicine, Maastricht University, Maastricht, The Netherlands.ORCID 0000-0003-0702-5609
Rhiannon GrantInstitute for Bioengineering, School of Engineering, University of Edinburgh, Edinburgh, UK.ORCID 0000-0003-1507-2042
Ana M Pereira DaoudDepartment of Medical Ethics and Health Law, Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0002-0675-8133

Funding

Dutch Organization for Health Research and DevelopmentDutch Organization for Health Research and Development 10250022120001Dutch Organization for Health Research and Development 10250022120002GREAT consortiumHipGametes consortiumNovo Nordisk Foundation Center for Stem Cell Medicine NNF21CC0073729reNEWStichting De WeijerhorstZonMw 10250022120001
6 · The paper itself

Abstract

backgroundStem cell-based embryo models (SCBEMs) are clusters of pluripotent stem cells that can mimic morphological and functional aspects of early human embryos to different degrees. When cultured from human cells, SCBEMs offer technically scalable and amenable tools that can help refine, reduce, and, in the future, perhaps replace the use of animals and human embryos in fundamental and clinical research. These advantages propelled the development of SCBEMs, and several distinct types have been generated over the past decade, including gastruloids, axioloids, blastoids, and post-implantation-like embryoids. For purposes of governance, advisory reports distinguish between SCBEMs based on their presumed capacity to continuously undergo organized human development-referred to here as developmental potential. However, since functionally testing this potential by transferring human SCBEMs to a uterus would be unethical and is recommended to be prohibited, scientists lack clear or consistent ways to assess it. OBJECTIVE AND RATIONALE: This narrative review aims to tackle the question of how to assess developmental potential in SCBEMs by clarifying the different ways in which it can be and is being conceptualized. We achieve this by synthesizing insights from governance, science, and ethics. First, we examine how developmental potential is described in contemporary governance frameworks, and which aspects are emphasized. Next, we discuss biological markers for developmental potential and show how their scientific basis (in embryos, let alone SCBEMs) remains poorly understood. Then, we explore how the aspects considered relevant for assessments of developmental potential in governance and science may pre-emptively hinge on underlying conceptual interpretations and lead to differing normative implications. SEARCH

methodsThis narrative review combines insights from both the academic and grey literature on the (ethics of) embryo models. Original and review articles were selected from PubMed and Biorxiv with the main focus on articles published since 2015. Search terms included: embryo quality, in vitro fertilization, Gardner system, blastoid, gastruloid, embryo research, potentiality argument, developmental potential, transcriptomics, epigenetics, embryo metabolism, and related terms. Additional sources were identified through snowballing. This work focuses predominantly on human SCBEMs, but references to animal models are made. OUTCOMES: Comparison of the descriptions currently recommended for governance suggests at least three criteria that are used to assess developmental potential in SCBEMs: composition, organization, and interaction. Scientifically, developmental potential is multifaceted and only partly characterized, making it necessary to measure a broader range of aspects, using human embryos as benchmarks when possible. Since the range and significance of these aspects can be shaped by underlying accounts of developmental potential, contemporary advisory reports are examined to explore if and how they connote interpretations of developmental potential as possibility, probability, and predisposition. WIDER IMPLICATIONS: Categorization of the regulatory and scientific criteria currently used to assess developmental potential shows that they are underpinned by distinct interpretations of the concept, revealing tensions and questions for further inquiry. By synthesizing insights from governance, science, and ethics, this review thus aims to contribute to the responsible advancement of the SCBEM field and to support its coherent and transparent governance. REGISTRATION NUMBER: N/A.

Indexed as

Embryo, MammalianEmbryonic DevelopmentModels, BiologicalPluripotent Stem CellsBenchmarkingHumansbenchmarksdevelopmental potentialethicsgovernancehuman stem cell-based embryo modelsintegrationscience

Identifiers

PMID41489619
PMCPMC13139666

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.