Skip to content
DraconiticResearch
Search Sources API
190,860 studies31 sourcesUpdated 35 min ago
Peer-reviewedCC BYFrontiers in toxicology

Exploring long noncoding RNAs as a molecular connection between immune response and autism spectrum disorder

  1. 1College of Human Medicine, Michigan State University , , ,

Abstract

Autism spectrum disorder (ASD) is a neurodevelopmental condition increasingly linked to immune dysregulation, with long noncoding RNAs (lncRNAs) emerging as potential regulators of both neural and immune processes. This study commenced by analyzing ten unique lncRNAs and integrated ASD whole-blood datasets using the online platform GTex to identify expression of lncRNAs in various tissues. Moreover, the platform Network Analyst was utilized to assess differentially expressed lncRNAs and associated transcriptomic networks. A total of 93 upregulated and 51 downregulated lncRNAs were identified in people with ASD with tissue specific enrichment observed for MSNP1AS and LNC01238 in immune related systems. The transcription factor CEBPA was shown to interact with the upregulated lncRNA MALAT1, which influenced immune cell differentiation, inflammation and cytokine signaling. Intriguingly CEBPA simultaneously interacted with downregulated lnc RNA MIR22HG. Comparatively, downregulated lncRNAs were associated with the transcription factors TEAD2, CEBPA, CTCF, E2F4, TFAP2C, HIF1A, ETS1, HNF4A, SNAPC4, STAT1, STAT2, TEAD2, FOXC1, BRCA1, AR, E2F4, EOMES, SPI1, DACH1, E2F1, TP63, HMAP1, KLF9, HDGF, and MAZ. Overall, the findings support a role for lncRNAs in ASD pathophysiology and immune dysregulation, pointing to their potential as biomarkers and potential therapeutic targets for future research.

Related

  1. Identification of Peripheral Blood mIR-128-3p Molecular Signature in Children with Autism Spectrum Disorder
    TN Popov, SD Minchev, TI Vachev
    Balkan journal of medical genetics : BJMGPeer-reviewedCC BYFull textGenetics & genomicsEurope PMC
  2. Exploring the role of readthrough-inducing molecule 2,6-diaminopurine to increase immune response against cancer cells
    Carmen Sandoval Pacheco, Alice Leroy, Mehdi Derhourhi +21
    Molecular TherapyPeer-reviewedCC BY2 citedImmunologyHAL
  3. TensorPLS: an R package for exploring molecular and temporal patterns in longitudinal omics data using PLS-DA
    A. Giordano, A. Conesa, L. Balzano Nogueira
    bioRxivPreprintCC BYFull textBioinformatics & computational biologybioRxiv
  4. Exploring piling behavior in aviary-housed laying hens in response to age, management practices, and social influences
    Valentina Bongiorno, Ahmed B.A. Ali, Janice M. Siegford
    Poultry SciencePeer-reviewedCC BY 4.0Full textZoology & animal behaviourPMC
  5. A reproducible buccal transcriptomic response to music exposure in autism spectrum disorder: insights into the oral-brain axis
    A. Gomez Carballa, N. E. Z. Mallah, L. Navarro +2
    bioRxivPreprintCC BY-NC-NDFull textGenetics & genomicsbioRxiv
BibTeX
@article{roschyk2026exploring,
  title = {{Exploring long noncoding RNAs as a molecular connection between immune response and autism spectrum disorder}},
  author = {Anaya Roschyk and Daniel B. Campbell},
  journal = {Frontiers in toxicology},
  year = {2026},
  month = oct,
  doi = {10.3389/ftox.2026.1893084},
  url = {https://europepmc.org/article/PMC/PMC13720281},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - Exploring long noncoding RNAs as a molecular connection between immune response and autism spectrum disorder
AU  - Anaya Roschyk
AU  - Daniel B. Campbell
PY  - 2026
DA  - 2026/10/16
JO  - Frontiers in toxicology
DO  - 10.3389/ftox.2026.1893084
UR  - https://europepmc.org/article/PMC/PMC13720281
AB  - Autism spectrum disorder (ASD) is a neurodevelopmental condition increasingly linked to immune dysregulation, with long noncoding RNAs (lncRNAs) emerging as potential regulators of both neural and immune processes. This study commenced by analyzing ten unique lncRNAs and integrated ASD whole-blood datasets using the online platform GTex to identify expression of lncRNAs in various tissues. Moreover, the platform Network Analyst was utilized to assess differentially expressed lncRNAs and associated transcriptomic networks. A total of 93 upregulated and 51 downregulated lncRNAs were identified in people with ASD with tissue specific enrichment observed for MSNP1AS and LNC01238 in immune related systems. The transcription factor CEBPA was shown to interact with the upregulated lncRNA MALAT1, which influenced immune cell differentiation, inflammation and cytokine signaling. Intriguingly CEBPA simultaneously interacted with downregulated lnc RNA MIR22HG. Comparatively, downregulated lncRNAs were associated with the transcription factors TEAD2, CEBPA, CTCF, E2F4, TFAP2C, HIF1A, ETS1, HNF4A, SNAPC4, STAT1, STAT2, TEAD2, FOXC1, BRCA1, AR, E2F4, EOMES, SPI1, DACH1, E2F1, TP63, HMAP1, KLF9, HDGF, and MAZ. Overall, the findings support a role for lncRNAs in ASD pathophysiology and immune dysregulation, pointing to their potential as biomarkers and potential therapeutic targets for future research.
SN  - 2673-3080
ER  -