Evidence map›Paper›PMID 41495107›Full record

ArticleScientific reports2026

Transcriptomic analysis of preimplantation mouse embryos exposed to nanoplastics using RNA sequencing.

Hyeong-Ju You, Yu-Jin Jo, Jeongwoo Kwon, Seung-Bin Yoon, Changsic Youn, Yejin Kim, Man-Jong Kang, Ji-Su Kim

Abstract read
In one paragraph

Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Hyeong-Ju You *Primate Resources Center (PRC), Korea Research Institute of Bioscience and Biotechnology (KRIBB), Nengme-gil 351-33, Jeongeup-si, 56216, Jeollabuk-do, Republic of Korea.
Yu-Jin Jo *Primate Resources Center (PRC), Korea Research Institute of Bioscience and Biotechnology (KRIBB), Nengme-gil 351-33, Jeongeup-si, 56216, Jeollabuk-do, Republic of Korea.
Jeongwoo KwonPrimate Resources Center (PRC), Korea Research Institute of Bioscience and Biotechnology (KRIBB), Nengme-gil 351-33, Jeongeup-si, 56216, Jeollabuk-do, Republic of Korea.
Seung-Bin YoonPrimate Resources Center (PRC), Korea Research Institute of Bioscience and Biotechnology (KRIBB), Nengme-gil 351-33, Jeongeup-si, 56216, Jeollabuk-do, Republic of Korea.
Changsic YounPrimate Resources Center (PRC), Korea Research Institute of Bioscience and Biotechnology (KRIBB), Nengme-gil 351-33, Jeongeup-si, 56216, Jeollabuk-do, Republic of Korea.
Yejin KimPrimate Resources Center (PRC), Korea Research Institute of Bioscience and Biotechnology (KRIBB), Nengme-gil 351-33, Jeongeup-si, 56216, Jeollabuk-do, Republic of Korea.
Man-Jong KangDepartment of Animal Science, Chonnam National University, 77, Yongbong-ro, Buk-gu, Gwangju, 61186, Korea. mjkang@chonnam.ac.kr.
Ji-Su KimPrimate Resources Center (PRC), Korea Research Institute of Bioscience and Biotechnology (KRIBB), Nengme-gil 351-33, Jeongeup-si, 56216, Jeollabuk-do, Republic of Korea. kimjs@kribb.re.kr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The increasing prevalence of nanoplastics (NPs) in the environment has raised concerns regarding their potential risks to ecosystems and human health. NP exposure has been shown to interfere with cellular processes; however, their effects on preimplantation embryonic development remain unclear. Given the critical role of zygotic genome activation and early cell cycle progression, disruption during this period can significantly affect embryonic viability. To investigate the molecular effects of polymethylmethacrylate (PMMA)-NPs on early embryonic development, mouse zygotes were exposed to 0.1 or 1 mg/mL PMMA-NPs, and RNA sequencing was performed on four-cell stage embryos. Differential gene expression analysis revealed that 0.1 mg/mL NP exposure affected genes related to DNA damage repair, transcriptional regulation, and cellular homeostasis while 1 mg/mL NP exposure altered the expression of genes associated with apoptotic signaling, cell cycle arrest, and failure of blastocyst formation, suggesting a concentration-dependent effect on developmental progression. Thus, PMMA-NP exposure disrupts early embryonic development by inducing specific transcriptomic changes that potentially affect genome integrity and developmental competency. This study provides new insights into the molecular mechanisms underlying NP-induced embryo toxicity and elucidates the effect of NPs on preimplantation embryo development.

Indexed as

BlastocystGene Expression ProfilingNanoparticlesTranscriptomeAnimalsEmbryonic DevelopmentFemaleGene Expression Regulation, DevelopmentalMiceSequence Analysis, RNAZygoteEmbryo RNA sequencingMouse embryo developmentNanoplastics

Identifiers

PMID41495107
PMCPMC12780008

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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.