Evidence map›Paper›PMID 40168074›Full record

ArticleJCI insight2025

Loss of GATA2 promotes invasion and predicts cancer recurrence and survival in uterine serous carcinoma.

Usha S Polaki, Trey E Gilpin, Apoorva T Patil, Emily Chiu, Ruth Baker, Peng Liu, Tatiana S Pavletich, Morteza Seifi, Paula M Mañán-Mejías, Jordan Morrissey and 13 more

Abstract read
In one paragraph

Article in JCI insight, 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

23 authors.

Usha S PolakiDepartment of Pathology and Laboratory Medicine and.
Trey E GilpinDepartment of Pathology and Laboratory Medicine and.
Apoorva T PatilDepartment of Pathology and Laboratory Medicine and.
Emily ChiuDepartment of Obstetrics and Gynecology, University of Wisconsin-Madison, Madison, Wisconsin USA.
Ruth BakerDepartment of Obstetrics, Gynecology, and Women's Health, University of Minnesota, Minneapolis, Minnesota, USA.
Peng LiuDepartment of Biostatistics and Medical Informatics and.
Tatiana S PavletichDepartment of Pathology and Laboratory Medicine and.
Morteza SeifiWisconsin State Laboratory of Hygiene, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.
Paula M Mañán-MejíasDepartment of Obstetrics and Gynecology, University of Wisconsin-Madison, Madison, Wisconsin USA.
Jordan MorrisseyDepartment of Pathology and Laboratory Medicine and.
Jenna PortDepartment of Pathology and Laboratory Medicine and.
Rene Welch SchwartzDepartment of Biostatistics and Medical Informatics and.
Irene M OngDepartment of Biostatistics and Medical Informatics and.
Dina El-RayesDepartment of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, Minnesota, USA.
Mahmoud A KhalifaDepartment of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, Minnesota, USA.
Pei HuiDepartment of Pathology, Yale University School of Medicine, New Haven, Connecticut, USA.
Vanessa L HornerDepartment of Pathology and Laboratory Medicine and.
María Virumbrales-MuñozDepartment of Obstetrics and Gynecology, University of Wisconsin-Madison, Madison, Wisconsin USA.
Britt K EricksonDepartment of Obstetrics, Gynecology, and Women's Health, University of Minnesota, Minneapolis, Minnesota, USA.
Lisa BarroilhetDepartment of Obstetrics and Gynecology, University of Wisconsin-Madison, Madison, Wisconsin USA.
Stephanie M McGregorDepartment of Pathology and Laboratory Medicine and.
Emery H BresnickDepartment of Cell and Regenerative Biology, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Daniel R MatsonDepartment of Pathology and Laboratory Medicine and.

Funding

UW COMPREHENSIVE CANCER CENTER SUPPORTP30CA014520 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI Justine Yang Bruce · 1985 to 2026
$142.6M
University of Minnesota Clinical and Translational Science Institute (UMN CTSI)UL1TR000114 · NCATS · UNIVERSITY OF MINNESOTA · PI BLAZAR, BRUCE R · 2012 to 2015
$35.0M
RESEARCH TRAINING IN HEMATOLOGYT32HL007899 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI Jane Ellen Churpek · 1998 to 2026
$8.2M
Hematopoietic Regulation via GATA SwitchesR01DK068634 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI Emery H. Bresnick · 2006 to 2026
$7.5M
Increasing access to cancer trials in Minnesota (InACT-MN)R50CA278811 · NCI · UNIVERSITY OF MINNESOTA · PI Britt Kristina Erickson · 2023 to 2026
$731k
The Role of the GATA2 Interactome in ErythropoiesisK08DK127244 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI MATSON, DANIEL R. · 2021 to 2025
$693k
Automated Tissue MicroarrayerS10OD023526 · OD · UNIVERSITY OF WISCONSIN-MADISON · PI MATKOWSKYJ, KRISTINA A. · 2018 to 2018
$184k
NCATS NIH HHS UL1 TR000114NCI NIH HHS P30 CA014520NCI NIH HHS R50 CA278811NHLBI NIH HHS T32 HL007899NIDDK NIH HHS K08 DK127244NIDDK NIH HHS R01 DK068634NIH HHS S10 OD023526
6 · The paper itself

Abstract

BACKGROUNDA priori knowledge of recurrence risk in patients with nonmetastatic (International Federation of Gynecology and Obstetrics [FIGO] stage I) uterine serous carcinoma (USC) would enable a risk-stratified approach to the use of adjuvant chemotherapy. This would greatly reduce treatment-related morbidity and be predicted to improve survival.METHODSGATA2 expression was scored by IHC across a retrospective multiinstitutional cohort of 195 primary USCs. Associations between GATA2 levels and clinicopathologic metrics were evaluated using Student's t test, Fisher's exact test, Kaplan-Meier method, and Cox proportional hazard ratio. Invasion in patient-derived USC cells was assessed by Student's t test. RNA-Seq, anti-GATA2 ChIP-Seq, and confirmatory Western blotting enabled identification of GATA2 targets.RESULTSPatients with FIGO stage I GATA2hi USCs had 100% recurrence-free and 100% cancer-related survival, which was significantly better than patients with GATA2lo USCs. In patients for whom adjuvant chemotherapy was omitted, patients with GATA2hi USC had 100% recurrence-free 5-year survival compared with 60% recurrence-free survival in patients with GATA2lo USC. Depletion of GATA2 in patient-derived USC cells increased invasion in vitro.CONCLUSIONRoutine GATA2 IHC identifies 33% of patients with FIGO stage I USC who have a greatly reduced risk of posthysterectomy USC recurrence. Our results suggest that a GATA2-guided personalized medicine approach could be rapidly implemented in most hospital settings, would reduce treatment-related morbidity, and would likely improve outcomes in patients with USC.FUNDINGNIH grants R01 DK068634, P30 CA014520, S10 OD023526, K08 DK127244, T32 HL007899, the UW-Madison Department of Pathology and Laboratory Medicine, the UW-Madison Centennial Scholars Program, the Diane Lindstrom Foundation, the American Cancer Society, the V Foundation, The Hartwell Foundation, and the UMN Department of Obstetrics, Gynecology, and Women's Health.

Indexed as

Cystadenocarcinoma, SerousGATA2 Transcription FactorNeoplasm Recurrence, LocalUterine NeoplasmsAgedBiomarkers, TumorFemaleHumansMiddle AgedNeoplasm InvasivenessPrognosisRetrospective StudiesBiomarkers, TumorGATA2 protein, humanGATA2 Transcription FactorCancerClinical ResearchObstetrics/gynecologyOncologyTumor suppressors

Identifiers

PMID40168074
PMCPMC12128953

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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.