Evidence mapPaperPMID 41516039Full record

ReviewInternational journal of molecular sciences2025

How Early-Life Programming During Embryogenesis Imprints Cellular Memory.

Norermi Firzana Alfian, Kei Uechi, Yoshiya Morishita, Kaname Sato, Maruhashi Yui, Jannatul Ferdous Jharna, Md Wasim Bari, Shiori Ishiyama, Kazuki Mochizuki, Satoshi Kishigami

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 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. Article
  2. 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

10 authors.

Norermi Firzana AlfianDepartment of Integrated Applied Life Science, Integrated Graduate School of Medicine, Engineering, and Agricultural Sciences, University of Yamanashi, Kofu 400-0016, Japan.ORCID 0009-0004-6493-669X
Kei UechiDepartment of Integrated Applied Life Science, Integrated Graduate School of Medicine, Engineering, and Agricultural Sciences, University of Yamanashi, Kofu 400-0016, Japan.
Yoshiya MorishitaDepartment of Integrated Applied Life Science, Integrated Graduate School of Medicine, Engineering, and Agricultural Sciences, University of Yamanashi, Kofu 400-0016, Japan.
Kaname SatoDepartment of Integrated Applied Life Science, Integrated Graduate School of Medicine, Engineering, and Agricultural Sciences, University of Yamanashi, Kofu 400-0016, Japan.
Maruhashi YuiDepartment of Integrated Applied Life Science, Integrated Graduate School of Medicine, Engineering, and Agricultural Sciences, University of Yamanashi, Kofu 400-0016, Japan.
Jannatul Ferdous JharnaDepartment of Integrated Applied Life Science, Integrated Graduate School of Medicine, Engineering, and Agricultural Sciences, University of Yamanashi, Kofu 400-0016, Japan.ORCID 0009-0004-9904-4253
Md Wasim BariFaculty of Life and Environmental Sciences, University of Yamanashi, Kofu 400-8510, Japan.ORCID 0000-0002-0813-3081
Shiori IshiyamaFaculty of Life and Environmental Sciences, University of Yamanashi, Kofu 400-8510, Japan.ORCID 0009-0006-9195-2331
Kazuki MochizukiFaculty of Life and Environmental Sciences, University of Yamanashi, Kofu 400-8510, Japan.ORCID 0000-0002-7929-4667
Satoshi KishigamiFaculty of Life and Environmental Sciences, University of Yamanashi, Kofu 400-8510, Japan.ORCID 0000-0001-9447-5100

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cellular memory, or epigenetic memory, represents the capacity for cells to retain information beyond the underlying DNA sequence. This heritable characteristic is primarily governed by epigenetic mechanisms which enable cells to maintain specialized characteristics across divisions. This persistent cellular state is essential for fundamental biological processes, such as maintaining tissue identity and facilitating cell differentiation, especially embryonic cells. Early-stage perturbations such as assisted reproductive technologies (ART) and nutritional stress links embryonic exposures to adult health and disease within the Developmental Origins of Health and Disease (DOHaD) framework. Crucially, memory established during early embryogenesis links these epigenetic modifications to adult long-term phenotypes related to metabolic disorders. These modifications-including DNA methylation, histone modifications, and non-coding RNAs-support cellular memory transmission across cell divisions, and in certain organisms, can be transmitted across generations without alterations to the DNA sequence. This review synthesizes recent advances in epigenetic pathways that mediate cellular memory, highlights critical preimplantation windows of vulnerability and outlines gaps necessary for mammalian developing interventions that safeguard future generations.

Indexed as

Embryonic DevelopmentEpigenesis, GeneticAnimalsDevelopmental Origins of Health and DiseaseDNA MethylationEpigenetic MemoryGene Expression Regulation, DevelopmentalHumanscellular memoryDOHaDembryogenesisepigenetic inheritance

Identifiers

PMID41516039
PMCPMC12786116

What Socratic 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 Socratic graph.