Evidence map›Paper›PMID 39691991›Full record

ArticleThe Journal of pathology2025

Genomic characterization and histologic analysis of uterine leiomyosarcoma arising from leiomyoma with bizarre nuclei.

Christopher Felicelli, Xinyan Lu, Zachary Coty-Fattal, Yue Feng, Ping Yin, Matthew John Schipma, Julie J Kim, Lawrence J Jennings, Serdar E Bulun, Jian-Jun Wei

Abstract read
In one paragraph

Article in The Journal of pathology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

10 authors.

Christopher FelicelliDepartment of Pathology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Xinyan LuDepartment of Pathology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Zachary Coty-FattalDepartment of Pathology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Yue FengDepartment of Pathology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Ping YinDepartment of Obstetrics and Gynecology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Matthew John SchipmaLurie Cancer Center, Northwestern University, Feinberg School of Medicine, Chicago, IL, USA.
Julie J KimDepartment of Obstetrics and Gynecology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Lawrence J JenningsDepartment of Pathology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Serdar E BulunDepartment of Obstetrics and Gynecology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Jian-Jun WeiDepartment of Pathology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.ORCID 0000-0003-0281-2793

Funding

Reactive Oxygen Species in the Initiation, Survival and Racial Disparity of Uterine LeiomyomaR01CA254367 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI KIM, JI-YONG JULIE, WEI, JIAN-JUN · 2020 to 2025
$2.9M
NCI NIH HHS R01 CA254367
6 · The paper itself

Abstract

Leiomyoma with bizarre nuclei (LM-BN) is a rare variant of leiomyoma with a benign clinical course. In contrast, leiomyosarcoma (LMS) is a high-grade, malignant neoplasm characterized by high recurrence rates and poor survival. While LM-BN and LMS show distinct morphologies, they share similar immunoprofiles and molecular alterations, with both considered 'genomically unstable'. Rare cases of LM-BN associated with LMS have been reported; however, the histogenesis and molecular relationship between these two tumors remains unclear. In this study, we assessed 11 cases of LMS arising in conjunction with LM-BN confirmed by histology and immunohistochemistry (IHC), further analyzed by clinical, histologic, and molecular characteristics of these distinct components. LM-BN and LMS had similar p16 and p53 IHC patterns, but LMS had a higher Ki-67 index and lower estrogen and progesterone eceptor expression. Digital image analysis based on cytologic features revealed spatial relationships between LMS and LM-BN. Genomic copy number alterations (CNAs) demonstrated the same clonal origin of LMS arising from existing LM-BN through conserved CNAs. LMS harbored highly complex CNAs and more frequent losses of the TP53, RB1, and PTEN genomic regions than LM-BN (p = 0.0031), with CDKN2A/B deletion identified in LMS only. Mutational profiling revealed many shared oncogenic alterations in both LM-BN and LMS; however, additional mutations were present within LMS, indicative of tumor progression through progressive genomic instability. Analysis of spatial transcriptomes defined uniquely expressed gene signatures that matched the geographic distribution of LM-BN, LMS, and other cell types. Our findings indicate for the first time that a subset of LMS arises from an existing LM-BN, and highly complex genomic alterations could be potential high risks associated with disease progression in LM-BN. © 2024 The Author(s). The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.

Indexed as

Cell NucleusLeiomyomaLeiomyosarcomaUterine NeoplasmsAdultAgedBiomarkers, TumorDNA Copy Number VariationsFemaleHumansImmunohistochemistryMiddle AgedBiomarkers, Tumorcopy number alterationdigital image analysisimmunohistochemistryleiomyoma with bizarre nucleioncogene sequencingspatial transcriptometumor progressionuterine leiomyosarcoma

Identifiers

PMID39691991
PMCPMC11717496

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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.