Evidence map›Paper›PMID 39273639›Full record

ArticleInternational journal of molecular sciences2024

Functional Analysis of RE1 Silencing Transcription Factor as a Putative Tumor Suppressor in Human Endometrial Cancer.

Yasmin Abedin, Paige Minchella, Riley Peterson, Francesca Gonnella, Amanda Graham, Ian Cook, Melissa Javellana, Andrea Jewell, Lori Spoozak, Warren B Nothnick

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. 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.

Yasmin AbedinDepartment of Obstetrics and Gynecology, University of Kansas Medical Center, Kansas City, KS 66160, USA.ORCID 0000-0001-7628-1919
Paige MinchellaDepartment of Cell Biology and Physiology, University of Kansas Medical Center, Kansas City, KS 66160, USA.
Riley PetersonDepartment of Cell Biology and Physiology, University of Kansas Medical Center, Kansas City, KS 66160, USA.
Francesca GonnellaDepartment of Cell Biology and Physiology, University of Kansas Medical Center, Kansas City, KS 66160, USA.
Amanda GrahamDepartment of Cell Biology and Physiology, University of Kansas Medical Center, Kansas City, KS 66160, USA.
Ian CookDepartment of Obstetrics and Gynecology, University of Kansas Medical Center, Kansas City, KS 66160, USA.
Melissa JavellanaDepartment of Obstetrics and Gynecology, University of Kansas Medical Center, Kansas City, KS 66160, USA.
Andrea JewellDepartment of Obstetrics and Gynecology, University of Kansas Medical Center, Kansas City, KS 66160, USA.ORCID 0000-0002-4752-6662
Lori SpoozakDepartment of Obstetrics and Gynecology, University of Kansas Medical Center, Kansas City, KS 66160, USA.ORCID 0000-0002-3359-7291
Warren B NothnickDepartment of Obstetrics and Gynecology, University of Kansas Medical Center, Kansas City, KS 66160, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Uterine cancer is the most common gynecologic malignancy in the United States, with endometrioid endometrial adenocarcinoma (EC) being the most common histologic sub-type. Considering the molecular classifications of EC, efforts have been made to identify additional biomarkers that can assist in diagnosis, prognosis, and individualized therapy. We sought to explore the relationship of Repressor Element 1 (RE1) silencing transcription factor (REST), which downregulates neuronal genes in non-neuronal tissue, along with matrix metalloproteinase-24 (MMP24) and EC. We analyzed the expression of REST and MMP24 in 31 cases of endometrial cancer and 16 controls. We then explored the baseline expression of REST and MMP24 in two EC cell lines (Ishikawa and HEC-1-A) compared to a benign cell line (t-HESC) and subsequently evaluated proliferation, migration, and invasion in the setting of loss of

Indexed as

Cell MovementCell ProliferationEndometrial NeoplasmsGene Expression Regulation, NeoplasticRepressor ProteinsAgedBiomarkers, TumorCell Line, TumorFemaleGenes, Tumor SuppressorHumansMiddle AgedNeoplasm InvasivenessRE1-Silencing Transcription FactorBiomarkers, TumorRE1-Silencing Transcription FactorRepressor Proteinsendometrial cancerendometrioid sub-typegene expressioninvasionmigrationMMP24proliferationprotein expressionREST

Identifiers

PMID39273639
PMCPMC11395688

What OpenQuestion holds

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LicenceCC BY
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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.