Evidence map›Paper›PMID 32998907›Full record

ArticleDisease models & mechanisms2020

Cells expressing PAX8 are the main source of homeostatic regeneration of adult mouse endometrial epithelium and give rise to serous endometrial carcinoma.

Dah-Jiun Fu, Andrea J De Micheli, Mallikarjun Bidarimath, Lora H Ellenson, Benjamin D Cosgrove, Andrea Flesken-Nikitin, Alexander Yu Nikitin

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Disease models & mechanisms, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.6field-weighted citation impact, top 8% 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

29 citing papers in PubMed, 44 citations in OpenAlex.

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  9. Phospholipid flippase ATP11A brokers uterine epithelial integrity and function.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Single-nuclei sequencing of uterine serous carcinoma reveals racial differences in immune signaling.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  15. Article
  16. Mechanisms of Regeneration and Fibrosis in the Endometrium.Annual review of cell and developmental biology · 2023
    Review
  17. Article
  18. Article
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  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Dah-Jiun FuDepartment of Biomedical Sciences, Cornell University, Ithaca, NY 14853, USA.
Andrea J De MicheliMeinig School of Biomedical Engineering, Cornell University, Ithaca, NY 14853, USA.ORCID 0000-0002-9985-2638
Mallikarjun BidarimathDepartment of Biomedical Sciences, Cornell University, Ithaca, NY 14853, USA.ORCID 0000-0002-9080-8737
Lora H EllensonMemorial Sloan-Kettering Cancer Center, New York, NY 10065, USA.
Benjamin D CosgroveMeinig School of Biomedical Engineering, Cornell University, Ithaca, NY 14853, USA.ORCID 0000-0003-2164-350X
Andrea Flesken-NikitinDepartment of Biomedical Sciences, Cornell University, Ithaca, NY 14853, USA af78@cornell.edu an58@cornell.edu.ORCID 0000-0003-3017-1399
Alexander Yu NikitinDepartment of Biomedical Sciences, Cornell University, Ithaca, NY 14853, USA af78@cornell.edu an58@cornell.edu.ORCID 0000-0002-3729-7982
Cornell University · USMemorial Sloan Kettering Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Revealing muscle stem cell heterogeneity in mice and humans through deep single-cell analysisR01AG058630 · NIA · CORNELL UNIVERSITY · PI COSGROVE, BENJAMIN DAVID · 2018 to 2022
$2.9M
Origins of Ovarian CarcinomaR01CA182413 · NCI · CORNELL UNIVERSITY · PI NIKITIN, ALEXANDER Y. · 2015 to 2019
$1.8M
Neuroendocrine mechanisms of prostate cancer progressionR01CA197160 · NCI · CORNELL UNIVERSITY · PI NIKITIN, ALEXANDER Y. · 2015 to 2020
$1.8M
NCI NIH HHS P30 CA008748NCI NIH HHS R01 CA182413NCI NIH HHS R01 CA197160NIA NIH HHS R01 AG058630
6 · The paper itself

Abstract

Humans and mice have cyclical regeneration of the endometrial epithelium. It is expected that such regeneration is ensured by tissue stem cells, but their location and hierarchy remain debatable. A number of recent studies have suggested the presence of stem cells in the mouse endometrial epithelium. At the same time, it has been reported that this tissue can be regenerated by stem cells of stromal/mesenchymal or bone marrow cell origin. Here, we describe a single-cell transcriptomic atlas of the main cell types of the mouse uterus and epithelial subset transcriptome and evaluate the contribution of epithelial cells expressing the transcription factor PAX8 to the homeostatic regeneration and malignant transformation of adult endometrial epithelium. According to lineage tracing, PAX8

Indexed as

HomeostasisRegenerationAgingAnimalsCell ProliferationDisease Models, AnimalEndometrial NeoplasmsEndometriumEpithelial CellsEpitheliumFemaleForkhead Transcription FactorsGene Expression ProfilingImmunophenotypingIntegrasesMice, TransgenicCre recombinaseForkhead Transcription FactorsFOXJ1 protein, mouseIntegrasesPAX8 Transcription FactorRNA, MessengerEndometrial cancerMouse modelsSingle-cell transcriptomeStem cells

Identifiers

PMID32998907
PMCPMC7648606
OpenAlexW3089364171

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.