OSCR

NAT10-dependent N<sup>4</sup>-acetylcytidine reprograms R-loops and promotes cancer stem cell growth.

Overview

Authors: Xujia Wu1,2, Donghai Wang1,3,2, Suchet Taori1,2, Weichi Wu1,3,2, Deobrat Dixit4, Deguan Lv1, Steven J Mullett5,6, Stacy L Gelhaus5,6, Fanen Yuan1, Po Zhang1, Tengfei Huang1,3, Huairui Yuan1, Qiulian Wu1,3, Jeremy N Rich1,3,7,8,9
ORCID iDs: Jeremy N Rich
  1. Hillman Cancer Center, University of Pittsburgh Medical Center, Pittsburgh, PA, USA
  2. These authors contributed equally
  3. Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC, USA
  4. Department of Neurology and Herbert Irving Comprehensive Cancer Center, Columbia University, New York, NY, USA
  5. Department of Pharmacology and Chemical Biology, University of Pittsburgh, Pittsburgh, PA, USA
  6. Health Sciences Mass Spectrometry Core, University of Pittsburgh, Pittsburgh, PA, USA
  7. Department of Neurology, University of Pittsburgh, Pittsburgh, PA, USA
  8. Department of Neurology, University of North Carolina, Chapel Hill, NC, USA
  9. Lead contact
Journal: Cell reports, volume 45, issue 6, article 117408
Dates: published online 1 June 2026; in print 23 June 2026
Type: Research article · Language: English
License: CC BY-NC-ND
Identifiers: DOI 10.1016/j.celrep.2026.117408 · PMID 42228575 · PMCID PMC13589288 · OpenAlex W7163083095
Open access: gold, a free copy (OpenAlex)
Status: data only
Categories: human (organism), mouse (organism), other condition (population), cellular / molecular (subfield)
Methods: Statistics, Smoothing, state filtering, decompositions, Machine learning, Preprocessing, Connectivity
Keywords: Glioblastoma, Cancer Stem Cell, Egr1, Glioblastoma Stem Cell, Epitranscriptomics, Nat10, Cp: Neuroscience, Cp: Cancer, Ac(4)c, R-loop Remodelin
MeSH: Cytidine*, Glioblastoma*, N-Terminal Acetyltransferase E*, Neoplastic Stem Cells*, R-Loop Structures*, Animals, Brain Neoplasms, Cell Line, Tumor, Cell Proliferation, Chromatin, Early Growth Response Protein 1, Gene Expression Regulation, Neoplastic, Humans, Mice, N-Terminal Acetyltransferases, Promoter Regions, Genetic (* major topic)
Topic: Cancer, Hypoxia, and Metabolism (Cancer Research, Biochemistry, Genetics and Molecular Biology), according to OpenAlex
Funding: Defense Health Agency Consortium (HT9425-23-1-0689); National Institutes of Health (R01CA238662, NIHS10OD032141, R01CA268634, R35CA197718, NIHS10OD023402, R01NS103434); NCI NIH HHS (R01 CA268634, R35 CA197718, R01 CA238662); NIH HHS (S10 OD032141, S10 OD023402); University of Pittsburgh; NINDS NIH HHS (R01 NS134724, R01 NS103434, R01 NS136424); Sun Yat-sen University; Wuhan University; American Cancer Society (CSCC-LEAD-22-186-01-CSCC)
Citations: cited by 2 papers (Europe PMC); 95 references in the paper
Research resources: RRID:AB_10949503, Mouse monoclonal anti-His tag RRID:AB_11232599, RRID:AB_2118010, Rabbit polyclonal anti-NAT10 RRID:AB_2148944, RRID:AB_2210206, RRID:AB_2616028, RRID:AB_2687463, Rabbit polyclonal anti-OLIG1 RRID:AB_2788135, RRID:AB_2819183, RRID:AB_2827750, Rabbit monoclonal anti-TBK1 RRID:AB_2863061, Rabbit monoclonal anti-Phospho-TBK1 RRID:AB_2863910, Rabbit monoclonal anti-Phospho-STING RRID:AB_2864054, Rabbit recombinant anti-V5 tag RRID:AB_2878059, RRID:AB_2879008, Rabbit polyclonal anti-EGR1 RRID:AB_2881272, Mouse monoclonal anti-VEGFA RRID:AB_2882171, Rabbit polyclonal anti-TAZ RRID:AB_2889852, Rabbit monoclonal anti-STING RRID:AB_3083450, Mouse monoclonal anti-Histone H3 RRID:AB_3086558, Rabbit polyclonal anti-Histone H2A.X RRID:AB_3102323, RRID:AB_3102500, RRID:AB_3105389, Rabbit polyclonal anti-PDGFA RRID:AB_3669576, Rabbit monoclonal anti-TNF-alpha (TNFα) RRID:AB_3670472, RRID:AB_3670503, Mouse monoclonal anti-WLS/GPR177 RRID:AB_3719304

Abstract

The abstract is not reproduced here: the paper's license (CC BY-NC-ND) does not allow it. Read it in the paper, at the publisher or on Europe PMC.

Code

The paper links to its data, not to its authors' code: see the Data section.

The paper's code and data availability statement is in the Data section.

Tracing map

A tracing map links a paper to the code its authors published: this paper has none, so it has no map.

Data

Datasets cited

Code and data availability statement

The paper has a code and data availability statement. Its license (CC BY-NC-ND) does not allow reproducing it here; in short, from what the harvester recognized in it:

Read it in the paper: doi.org/10.1016/j.celrep.2026.117408.

Versions

The history of this record: each version stored by the harvester or made by a correction of its authors or of the maintainers of its code, and what changed in its facts. The texts of the paper (its abstract, its availability statements) are not part of it; versions that changed only those are not listed.

Version 2, 28 September 2026

  • Publisher: — → Cell Press
  • Authors: added Jeremy N Rich (0000-0001-7845-5302); removed Jeremy N Rich

Version 1, 27 September 2026: the first record

Recorded: type, language, journal, volume, issue, pages, dates, 14 authors, 10 keywords, 16 MeSH terms, 9 funders, 94 references, 27 RRIDs.

Cite

This paper

Wu, X., Wang, D., Taori, S., Wu, W., Dixit, D., Lv, D., Mullett, S. J., Gelhaus, S. L., Yuan, F., Zhang, P., Huang, T., Yuan, H., Wu, Q., & Rich, J. N. (2026). NAT10-dependent N<sup>4</sup>-acetylcytidine reprograms R-loops and promotes cancer stem cell growth. Cell reports, 45(6), 117408. https://doi.org/10.1016/j.celrep.2026.117408

BibTeX

@article{wu2026nat10,
author = {Wu, Xujia and Wang, Donghai and Taori, Suchet and Wu, Weichi and Dixit, Deobrat and Lv, Deguan and Mullett, Steven J and Gelhaus, Stacy L and Yuan, Fanen and Zhang, Po and Huang, Tengfei and Yuan, Huairui and Wu, Qiulian and Rich, Jeremy N},
title = {{NAT10-dependent N\<sup\>4\</sup\>-acetylcytidine reprograms R-loops and promotes cancer stem cell growth}},
journal = {Cell reports},
year = {2026},
month = jun,
volume = {45},
number = {6},
pages = {117408},
publisher = {Cell Press},
issn = {2211-1247},
doi = {10.1016/j.celrep.2026.117408},
url = {https://doi.org/10.1016/j.celrep.2026.117408},
pmid = {42228575},
pmcid = {PMC13589288}
}

RIS

TY - JOUR
AU - Wu, Xujia
AU - Wang, Donghai
AU - Taori, Suchet
AU - Wu, Weichi
AU - Dixit, Deobrat
AU - Lv, Deguan
AU - Mullett, Steven J
AU - Gelhaus, Stacy L
AU - Yuan, Fanen
AU - Zhang, Po
AU - Huang, Tengfei
AU - Yuan, Huairui
AU - Wu, Qiulian
AU - Rich, Jeremy N
TI - NAT10-dependent N<sup>4</sup>-acetylcytidine reprograms R-loops and promotes cancer stem cell growth
T2 - Cell reports
J2 - Cell Rep
PY - 2026
DA - 2026/06/01
VL - 45
IS - 6
SP - 117408
SN - 2211-1247
PB - Cell Press
DO - 10.1016/j.celrep.2026.117408
UR - https://doi.org/10.1016/j.celrep.2026.117408
LA - en
ER -

CSL-JSON

{
"id": "10.1016/j.celrep.2026.117408",
"type": "article-journal",
"title": "NAT10-dependent N<sup>4</sup>-acetylcytidine reprograms R-loops and promotes cancer stem cell growth",
"container-title": "Cell reports",
"author": [
{
"family": "Wu",
"given": "Xujia"
},
{
"family": "Wang",
"given": "Donghai"
},
{
"family": "Taori",
"given": "Suchet"
},
{
"family": "Wu",
"given": "Weichi"
},
{
"family": "Dixit",
"given": "Deobrat"
},
{
"family": "Lv",
"given": "Deguan"
},
{
"family": "Mullett",
"given": "Steven J"
},
{
"family": "Gelhaus",
"given": "Stacy L"
},
{
"family": "Yuan",
"given": "Fanen"
},
{
"family": "Zhang",
"given": "Po"
},
{
"family": "Huang",
"given": "Tengfei"
},
{
"family": "Yuan",
"given": "Huairui"
},
{
"family": "Wu",
"given": "Qiulian"
},
{
"family": "Rich",
"given": "Jeremy N"
}
],
"container-title-short": "Cell Rep",
"volume": "45",
"issue": "6",
"page": "117408",
"DOI": "10.1016/j.celrep.2026.117408",
"PMID": "42228575",
"PMCID": "PMC13589288",
"ISSN": "2211-1247",
"publisher": "Cell Press",
"URL": "https://doi.org/10.1016/j.celrep.2026.117408",
"language": "en",
"issued": {
"date-parts": [
[
2026,
6,
1
]
]
}
}

Similar papers

The papers with a page that share the most with this one: the tools found in their code, their categories, datasets, cited references and authors, the rarest counting most.

[1] doi:10.1038/s41467-026-74058-0
IQGAP3 bridges matrix stiffness with glioma stem cell maintenance and radioresistance by stabilizing SOX2.
Journal: Nature communications
In common: other condition, mouse, cellular / molecular, 8 references, author Jeremy N Rich
[2] doi:10.1016/j.xcrm.2026.102766 [code]
A longitudinal single-cell and spatial multiomic atlas of pediatric high-grade glioma.
Journal: Cell reports. Medicine
In common: other condition, cellular / molecular, 6 references
[3] doi:10.1371/journal.pgen.1012081
ADNP regulates chromatin architecture and lineage fidelity during neural differentiation.
Journal: PLoS genetics
In common: mouse, 5 references
[4] doi:10.1038/s41467-026-74124-7 [code]
Glioma-intrinsic MAPK/ERK signaling promotes immunotherapy efficacy through T cell infiltration and interferon responses.
Journal: Nature communications
In common: other condition, mouse, 4 references
[5] doi:10.1016/j.stemcr.2026.103049
A human-specific non-coding RNA for EFHC1, an epilepsy-associated gene, regulates neural stem cell proliferation for cortical development.
Journal: Stem cell reports
In common: mouse, 4 references
[6] doi:10.1172/jci.insight.198298
Development and characterization of triazole-based WDR5 inhibitors for the treatment of glioblastoma.
Journal: JCI insight
In common: other condition, mouse, 3 references
[7] doi:10.32604/or.2026.079221
Single-Cell Sequencing Reveals the Heterogeneity of Glioma and Identifies IGFBP2 as A Potential Therapeutic Target.
Journal: Oncology research
In common: other condition, mouse, cellular / molecular, 4 references
[8] doi:10.1242/jcs.264529
Increased Glycine-N-methyltransferase expression disrupts light-dependent gene expression rhythms in the Drosophila eye.
Journal: Journal of cell science
In common: cellular / molecular, 5 references
[9] doi:10.1002/1878-0261.70223
EDNRB-dependent endothelin signaling reduces proliferation and promotes proneural-to-mesenchymal transition in gliomas.
Journal: Molecular oncology
In common: other condition, cellular / molecular, 4 references
[10] doi:10.1038/s41467-026-71803-3 [code]
Charting the transition from in vitro gliogenesis to the in vivo maturation of human glial progenitor cells transplanted into the hypomyelinated mouse brain.
Journal: Nature communications
In common: mouse, cellular / molecular, 4 references

Contribute

The authors of this paper can claim it, correct its record and validate its tracing map, and the maintainers of its code (its owner, or a public member of its organization) correct what it says of their repository; anyone signed in can ask for its removal. Every request goes to OSCR's own machine, which answers it; your account page follows them.

Sign in with ORCID to claim this paper as one of its authors, correct its record or validate its tracing map: when the paper's metadata lists your ORCID iD, you are recognized at once. Maintainers of its code: sign in with GitHub, then claim the repository on your account page.

Request its removal

To ask OSCR to remove this record, the copies of its authors' scripts or its tracing map, use the removal request page: signed in, you say who you are, what to remove and why, then review and confirm the request. Published rules decide every request (how).

Discussion, reproductions, activity

Discussion: questions and error reports about this paper and its code, from signed-in readers and its authors. It opens with sign-in.

Reproductions: reports from readers who ran the authors' code: what they reproduced, with which environment, commit and data. It opens with sign-in.

Activity: what happens around this paper: new versions of its record, its map's validation, discussions and reproductions. It opens with sign-in.