Evidence map›Paper›PMID 41424301›Full record

ArticleHistopathology2026

GREB1-rearranged uterine tumour shares a common DNA methylation signature with ESR1-rearranged UTROSCT.

Cheng-Han Lee, Yow-Shan Lee, Jennifer A Bennett, David L Kolin, Jen-Chieh Lee, Hsuan-Ying Huang, Martin Köbel, Mark Sementsov, Brendan C Dickson, Christian Koelsche and 3 more

Abstract read
In one paragraph

Article in Histopathology, 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. 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

13 authors.

Cheng-Han LeeDepartment of Laboratory Medicine and Pathology, University of Alberta, Edmonton, Alberta, Canada.ORCID https://orcid.org/0000-0003-2094-1222
Yow-Shan LeeDepartment of Family Medicine, Cathay General Hospital, Taipei, Taiwan.ORCID https://orcid.org/0009-0003-7470-8319
Jennifer A BennettUniversity of Chicago Medical Center, Chicago, Illinois, USA.ORCID https://orcid.org/0000-0001-8155-7131
David L KolinDivision of Women's and Perinatal Pathology, Department of Pathology, Brigham and Women's Hospital, Boston, Massachusetts, USA.ORCID https://orcid.org/0000-0002-7631-6525
Jen-Chieh LeeDepartment of Pathology, National Taiwan University Hospital, National Taiwan University College of Medicine, Taipei, Taiwan.ORCID https://orcid.org/0000-0001-7739-5934
Hsuan-Ying HuangDepartment of Anatomic Pathology, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung, Taiwan.ORCID https://orcid.org/0000-0002-1216-7751
Martin KöbelDepartment of Pathology and Laboratory Medicine, University of Calgary, Calgary, Alberta, Canada.ORCID https://orcid.org/0000-0002-6615-2037
Mark SementsovInstitute of Pathology, Heidelberg University Hospital, Heidelberg, Germany.ORCID https://orcid.org/0009-0006-8591-2237
Brendan C DicksonDepartment of Pathology and Laboratory Medicine, Sinai Health System and University of Toronto, Toronto, Ontario, Canada.ORCID https://orcid.org/0000-0003-2269-6216
Christian KoelscheInstitute of Pathology, Ludwig Maximilians University Hospital Munich, Munich, Germany.ORCID https://orcid.org/0000-0001-8763-8864
Friedrich KommossInstitute of Pathology, Medizin Campus Bodensee, Friedrichshafen, Germany.
Andreas von DeimlingDepartment of Neuropathology, Heidelberg University Hospital, Heidelberg, Germany.ORCID https://orcid.org/0000-0002-5863-540X
Felix K F KommossInstitute of Pathology, Heidelberg University Hospital, Heidelberg, Germany.ORCID https://orcid.org/0000-0003-0876-9087

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesGREB1-rearranged uterine tumours encompass a group of uterine mesenchymal tumours with varied histologic appearances. The fusion partners to GREB1 include NCOA1-3, SS18 and NR4A3. Given that some GREB1-rearranged uterine tumours exhibit histologic features of uterine tumours resembling ovarian sex cord tumour (UTROSCT), there is a general belief that GREB1-rearranged uterine mesenchymal tumours are part of the UTROSCT family.

methodsIn this study, we applied global DNA methylation and copy number analyses to a series of 10 GREB1-rearranged uterine tumours and 21 classic UTROSCTs (7 of which were molecularly confirmed to harbour ESR1::NCOA2/3 fusions).

resultsWe found that GREB1-rearranged uterine tumors show an overlap in their global methylation profiles with UTROSCT, including ESR1::NCOA2/3 positive cases. Together, these tumours form a DNA methylation cluster separate from uterine smooth muscle tumours (leiomyomas and leiomyosarcomas), endometrial stromal sarcomas (low-grade and high-grade), embryonal rhabdomyosarcoma and SMARCA4-deficient uterine sarcomas. However, despite their epigenetic similarity, there were two notable differences. First, GREB1-rearranged uterine tumours as a group displayed a greater degree of genomic complexity with more extensive copy number alterations than conventional UTROSCTs, including those harbouring ESR1::NCOA2/3. Second, GREB1-rearranged uterine tumours frequently lacked overt sex cord morphology: while all 7 ESR1::NCOA2/3 UTROSCTs demonstrated corded, nested, trabecular and/or tubular/sertoliform patterns, only 1 GREB1-rearranged uterine tumour displayed a prominent trabecular pattern, with the remaining cases showing exclusively or predominantly diffuse/solid growth.

conclusionsOverall, our findings confirm that GREB1-rearranged uterine tumours are part of the UTROSCT spectrum, though they frequently exhibit a more diffuse growth pattern and a higher degree of genomic instability.

Indexed as

DNA MethylationEstrogen Receptor alphaNeoplasm ProteinsSex Cord-Gonadal Stromal TumorsUterine NeoplasmsAdultFemaleGene RearrangementHumansMiddle AgedNuclear Receptor Coactivator 2ESR1 protein, humanEstrogen Receptor alphaGREB1 protein, humanNCOA2 protein, humanNeoplasm ProteinsNuclear Receptor Coactivator 2DNA methylationESR1GREB1uterine sarcomaUTROSCT

Identifiers

PMID41424301
PMCPMC12975671

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.