Evidence map›Paper›PMID 34376780›Full record

ArticleLaboratory investigation; a journal of technical methods and pathology2021

A novel human endometrial epithelial cell line for modeling gynecological diseases and for drug screening.

Youngran Park, Jin-Gyoung Jung, Zheng-Cheng Yu, Ryoichi Asaka, Wenjing Shen, Yeh Wang, Wei-Hung Jung, Alicja Tomaszewski, Geoff Shimberg, Yun Chen and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Laboratory investigation; a journal of technical methods and pathology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

19 citing papers in PubMed, 28 citations in OpenAlex.

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  18. Strategies for modelling endometrial diseases.Nature reviews. Endocrinology · 2022
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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

14 authors at 1 institution in 1 country.

Youngran ParkDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Jin-Gyoung JungDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Zheng-Cheng YuDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Ryoichi AsakaDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.ORCID 0000-0003-4450-5142
Wenjing ShenDepartment of Gynecology and Obstetrics, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Yeh WangDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Wei-Hung JungDepartment of Mechanical Engineering, Johns Hopkins University, Baltimore, MD, USA.
Alicja TomaszewskiDepartment of Gynecology and Obstetrics, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Geoff ShimbergDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Yun ChenDepartment of Mechanical Engineering, Johns Hopkins University, Baltimore, MD, USA.ORCID 0000-0001-6917-7814
Vamsi ParimiDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Stephanie GaillardDepartment of Gynecology and Obstetrics, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Ie-Ming ShihDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA. ishih@jhmi.edu.
Tian-Li WangDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA. tlw@jhmi.edu.ORCID 0000-0002-7082-449X
Johns Hopkins University · US

Funding

SPORE in Ovarian CancerP50CA228991 · NCI · JOHNS HOPKINS UNIVERSITY · PI Amanda Nickles Fader · 2018 to 2026
$20.5M
Role of cancer-associated mutations in endometriosisR01HD096147 · NICHD · JOHNS HOPKINS UNIVERSITY · PI SEGARS, JAMES H., SHIH, IE-MING · 2019 to 2023
$3.4M
Experimental Therapeutics by targeting Spleen Tyrosine KinaseR01CA215483 · NCI · JOHNS HOPKINS UNIVERSITY · PI SHIH, IE-MING · 2017 to 2021
$1.9M
Tension-Sensitive Drug Release System to Enhance Targeting SelectivityR21EB029677 · NIBIB · JOHNS HOPKINS UNIVERSITY · PI CHEN, YUN · 2020 to 2020
$610k
Acquisition of a Cyfuse Regenova 3D Bio-printerS10OD025193 · OD · JOHNS HOPKINS UNIVERSITY · PI CHEN, YUN · 2019 to 2019
$401k
Engineered Fibroblasts as Cell Therapy to Treat Colorectal Cancer via Tumor Stroma StabilizationF99CA253759 · NCI · JOHNS HOPKINS UNIVERSITY · PI JUNG, WEI-HUNG · 2020 to 2021
$93k
NCI NIH HHS F99 CA253759NCI NIH HHS P50 CA228991NCI NIH HHS R01 CA215483NIBIB NIH HHS R21 EB029677NICHD NIH HHS R01 HD096147NIH HHS S10 OD025193
6 · The paper itself

Abstract

Endometrium-related malignancies including uterine endometrioid carcinoma, ovarian clear cell carcinoma and ovarian endometrioid carcinoma are major types of gynecologic cancer, claiming more than 13,000 women's lives annually in the United States. In vitro cell models that recapitulate "normal" endometrial epithelial cells and their malignant counterparts are critically needed to facilitate the studies of pathogenesis in endometrium-related carcinomas. To achieve this objective, we have established a human endometrial epithelial cell line, hEM3, through immortalization and clonal selection from a primary human endometrium culture. hEM3 exhibits stable growth in vitro without senescence. hEM3 expresses protein markers characteristic of the endometrial epithelium, and they include PAX8, EpCAM, cytokeratin 7/8, and ER. hEM3 does not harbor pathogenic germline mutations in genes involving DNA mismatch repair (MMR) or homologous repair (HR) pathways. Despite its unlimited capacity of in vitro proliferation, hEM3 cells are not transformed, as they are not tumorigenic in immunocompromised mice. The cell line is amenable for gene editing, and we have established several gene-specific knockout clones targeting ARID1A, a tumor suppressor gene involved in the SWI/SNF chromatin remodeling. Drug screening demonstrates that both HDAC inhibitor and PARP inhibitor are effective in targeting cells with ARID1A deletion. Together, our data support the potential of hEM3 as a cell line model for studying the pathobiology of endometrium-related diseases and for developing effective precision therapies.

Indexed as

Cell LineDrug Evaluation, PreclinicalEpithelial CellsAnimalsEndometriumFemaleHumansMiceReceptors, EstrogenReceptors, Estrogen

Identifiers

PMID34376780
PMCPMC8720294
OpenAlexW3188434637

What OpenQuestion holds

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Read underepoch 390

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.