Evidence map›Paper›PMID 40221170›Full record

ArticleGynecologic oncology2025

An inducible FOXL2-dependent mouse model of ovarian adult type granulosa cell tumor.

Jian Li, Thomas Welte, Katherine Calzoncinth, Veena K Vuttaradhi, Allison L Brodsky, Kwong-Kwok Wong, Manu M Sebastian, Barrett Lawson, Charles V Kingsley, R Tyler Hillman

Abstract read
In one paragraph

Article in Gynecologic oncology, 2025. 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

10 authors.

Jian LiDepartment of Gynecologic Oncology and Reproductive Medicine, Division of Surgery, The University of Texas M.D. Anderson Cancer Center, Houston, TX, United States of America.
Thomas WelteDepartment of Gynecologic Oncology and Reproductive Medicine, Division of Surgery, The University of Texas M.D. Anderson Cancer Center, Houston, TX, United States of America.
Katherine CalzoncinthDepartment of Gynecologic Oncology and Reproductive Medicine, Division of Surgery, The University of Texas M.D. Anderson Cancer Center, Houston, TX, United States of America.
Veena K VuttaradhiDepartment of Gynecologic Oncology and Reproductive Medicine, Division of Surgery, The University of Texas M.D. Anderson Cancer Center, Houston, TX, United States of America.
Allison L BrodskyDepartment of Gynecologic Oncology and Reproductive Medicine, Division of Surgery, The University of Texas M.D. Anderson Cancer Center, Houston, TX, United States of America.
Kwong-Kwok WongDepartment of Gynecologic Oncology and Reproductive Medicine, Division of Surgery, The University of Texas M.D. Anderson Cancer Center, Houston, TX, United States of America.
Manu M SebastianDepartment of Veterinary Medicine and Surgery, Division of Discovery Science, The University of Texas MD Anderson Cancer Center, Houston, TX, United States of America.
Barrett LawsonDepartment of Pathology, Division of Pathology/Lab Medicine, University of Texas MD Anderson Cancer Center, Houston, TX, United States of America.
Charles V KingsleyDepartment of Imaging Physics, Small Animal Imaging Research Facility, University of Texas MD Anderson Cancer Center, Houston, TX, United States of America.
R Tyler HillmanDepartment of Gynecologic Oncology and Reproductive Medicine, Division of Surgery, The University of Texas M.D. Anderson Cancer Center, Houston, TX, United States of America; Department of Genomic Medicine, Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, United States of America; CPRIT Scholar in Cancer Research, Houston, TX, United States of America. Electronic address: rthillman@mdanderson.org.

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
Training of Academic Gynecologic OncologistsT32CA101642 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI ANIL K SOOD, Kathleen Schmeler · 2005 to 2026
$9.2M
NCI NIH HHS P30 CA016672NCI NIH HHS T32 CA101642
6 · The paper itself

Abstract

backgroundAdult-type granulosa cell tumors (AGCTs) are rare ovarian sex cord/stromal tumors with near-universal hotspot mutations in FOXL2 (c.C402G; p.Cys134Trp). Progress in the treatment of relapsed AGCT has been hindered by the lack of high-fidelity FOXL2-based mouse models. To address this critical unmet need, we created and validated a genetically engineered inducible mouse model of the human FOXL2 mutation that recapitulates the key features of the human disease.

methodsGene targeting in embryonic stem cells was used to introduce a Cre-inducible Foxl2

resultsFemale Amhr2-Cre; Foxl2

conclusionsA Amhr2-Cre; Foxl2

Indexed as

Disease Models, AnimalForkhead Box Protein L2Granulosa Cell TumorOvarian NeoplasmsAnimalsFemaleHumansMagnetic Resonance ImagingMiceMice, TransgenicMutationForkhead Box Protein L2FOXL2 protein, humanFoxl2 protein, mouseGranulosa cell tumorMouse modelTranslational science

Identifiers

PMID40221170
PMCPMC12246815

What OpenQuestion holds

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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.