Evidence map›Paper›PMID 37716459›Full record

ArticleThe Journal of steroid biochemistry and molecular biology2023

Global expression analysis of endometrial cancer cells in response to progesterone identifies new therapeutic targets.

Kristina W Thiel, Andreea M Newtson, Eric J Devor, Yuping Zhang, Paige K Malmrose, Jianling Bi, Haley A Losh, Suzy Davies, Lane E Smith, Jamie Padilla and 8 more

Open access · greenAbstract read
In one paragraph

Article in The Journal of steroid biochemistry and molecular biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 26% of its field
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

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

18 authors at 6 institutions in 1 country.

Kristina W ThielDepartment of Obstetrics and Gynecology, Carver College of Medicine, University of Iowa, Iowa City, IA, USA; Holden Comprehensive Cancer Center, University of Iowa, Iowa City, IA, USA.
Andreea M NewtsonDepartment of Obstetrics and Gynecology, Carver College of Medicine, University of Iowa, Iowa City, IA, USA; Department of Obstetrics and Gynecology, University of Nebraska, Omaha, NE, USA.
Eric J DevorDepartment of Obstetrics and Gynecology, Carver College of Medicine, University of Iowa, Iowa City, IA, USA; Holden Comprehensive Cancer Center, University of Iowa, Iowa City, IA, USA.
Yuping ZhangDepartment of Obstetrics and Gynecology, Carver College of Medicine, University of Iowa, Iowa City, IA, USA.
Paige K MalmroseDepartment of Obstetrics and Gynecology, Carver College of Medicine, University of Iowa, Iowa City, IA, USA.
Jianling BiDepartment of Obstetrics and Gynecology, Carver College of Medicine, University of Iowa, Iowa City, IA, USA.
Haley A LoshDepartment of Obstetrics and Gynecology, Carver College of Medicine, University of Iowa, Iowa City, IA, USA.
Suzy DaviesDepartment of Neurosciences, University of New Mexico Health Sciences Center, Albuquerque, NM, USA.
Lane E SmithDepartment of Internal Medicine, University of New Mexico Health Sciences Center, Albuquerque, NM, USA; University of New Mexico Comprehensive Cancer Center, Albuquerque, NM, USA.
Jamie PadillaDepartment of Internal Medicine, University of New Mexico Health Sciences Center, Albuquerque, NM, USA; University of New Mexico Comprehensive Cancer Center, Albuquerque, NM, USA.
Stephanie M LeivaDepartment of Obstetrics and Gynecology, Carver College of Medicine, University of Iowa, Iowa City, IA, USA.
Chad E GrueterDepartment of Internal Medicine, Carver College of Medicine, the University of Iowa, Iowa City, IA, USA.
Patrick BrehenyHolden Comprehensive Cancer Center, University of Iowa, Iowa City, IA, USA; Department of Biostatistics, College of Public Health, University of Iowa, Iowa City, IA, USA.
Christy R HaganDepartment of Biochemistry and Molecular Biology, University of Kansas Medical Center, Kansas City, KS, USA.
Miles A PufallDepartment of Biochemistry and Molecular Biology, University of Iowa, Iowa City, IA, USA.
Jason GertzDepartment of Oncological Sciences, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.
Yan GuoUniversity of New Mexico Comprehensive Cancer Center, Albuquerque, NM, USA.
Kimberly K LeslieDepartment of Obstetrics and Gynecology, Carver College of Medicine, University of Iowa, Iowa City, IA, USA; Holden Comprehensive Cancer Center, University of Iowa, Iowa City, IA, USA; Department of Internal Medicine, University of New Mexico Health Sciences Center, Albuquerque, NM, USA; University of New Mexico Comprehensive Cancer Center, Albuquerque, NM, USA. Electronic address: kkleslie@unm.salud.edu.
University of Iowa · USUniversity of New Mexico · USNew Mexico Cancer Center · USUniversity of Kansas Medical Center · USUniversity of Nebraska at Omaha · USUniversity of Utah · US

Funding

Viral VectorP30CA086862 · NCI · UNIVERSITY OF IOWA · PI Jon C.D. Houtman · 2000 to 2026
$70.0M
Route 66 Endometrial Cancer SPOREP50CA265793 · NCI · WASHINGTON UNIVERSITY · PI Esther Jiaxin Lu · 2023 to 2026
$11.6M
Targeted Therapy for Endometrial CancerR01CA099908 · NCI · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI LESLIE, KIMBERLY K. · 2002 to 2023
$5.8M
In situ evaluation of combinatorial gene regulation in the human genomeR01HG008974 · NHGRI · UNIVERSITY OF UTAH · PI GERTZ, JASON · 2017 to 2021
$3.2M
Attacking aggressive p53 mutants in gynecologic cancerK22CA263783 · NCI · UNIVERSITY OF IOWA · PI THIEL, KRISTINA W · 2022 to 2024
$561k
Optimal DNA Brain-Penetrating Nanoparticle (DNA-BPN) Formulation for Glioblastoma (GBM) TreatmentF31CA210610 · NCI · JOHNS HOPKINS UNIVERSITY · PI NEGRON, KARINA · 2016 to 2018
$125k
NCI NIH HHS F31 CA210610NCI NIH HHS K22 CA263783NCI NIH HHS P30 CA086862NCI NIH HHS P50 CA265793NCI NIH HHS R01 CA099908NHGRI NIH HHS R01 HG008974
6 · The paper itself

Abstract

Progesterone prevents development of endometrial cancers through its receptor (PR) although the molecular mechanisms have yet to be fully characterized. In this study, we performed a global analysis of gene regulation by progesterone using human endometrial cancer cells that expressed PR endogenously or exogenously. We found progesterone strongly inhibits multiple components of the platelet derived growth factor receptor (PDGFR), Janus kinase (JAK), signal transducer and activator of transcription (STAT) pathway through PR. The PDGFR/JAK/STAT pathway signals to control numerous downstream targets including AP-1 transcription factors Fos and Jun. Treatment with inhibitors of the PDGFR/JAK/STAT pathway significantly blocked proliferation in multiple novel patient-derived organoid models of endometrial cancer, and activation of this pathway was found to be a poor prognostic signal for the survival of patients with endometrial cancer from The Cancer Genome Atlas. Our study identifies this pathway as central to the growth-limiting effects of progesterone in endometrial cancer and suggests that inhibitors of PDGFR/JAK/STAT should be considered for future therapeutic interventions.

Indexed as

Endometrial NeoplasmsJanus KinasesFemaleHumansProgesteroneSignal TransductionSTAT Transcription FactorsJanus KinasesProgesteroneSTAT Transcription FactorsEndometrial cancerFosJanus kinase (JAK)JunPlatelet derived growth factor receptor (PDGFR)Progesterone receptor (PR)Signal transducer and activator of transcription (STAT)

Identifiers

PMID37716459
PMCPMC11171468
OpenAlexW4386783150

What OpenQuestion holds

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Registered trials

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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.