Evidence map›Paper›PMID 32934200›Full record

ArticleNature communications2020

TET2 directs mammary luminal cell differentiation and endocrine response.

Mi Ran Kim, Meng-Ju Wu, Yingsheng Zhang, Jer-Yen Yang, Chun Ju Chang

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

35 citing papers in PubMed, 48 citations in OpenAlex.

  1. Review
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  13. Mechanisms of Regulation of Cell Fate in Breast Development and Cancer.Advances in experimental medicine and biology · 2025
    Review
  14. Review
  15. Review
  16. Selective Estrogen Receptor Modulators' (SERMs) Influence onInternational journal of molecular sciences · 2024
    Article
  17. Article
  18. Article
  19. Review
  20. Review
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

5 authors at 4 institutions in 2 countries.

Mi Ran Kim *School of Sciences, Arts & Education, Ivy Tech Community College, Lafayette, IN, USA.
Meng-Ju Wu *Center for Cancer Research, Massachusetts General Hospital, Boston, MA, USA.
Yingsheng ZhangDepartment of Medicine and Biological Sciences, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Jer-Yen YangGraduate Institute of Biomedical Sciences, College of Medicine, China Medical University, Taichung, 40402, Taiwan. jyyang@mail.cmu.edu.tw.ORCID http://orcid.org/0000-0003-2789-8888
Chun Ju ChangGraduate Institute of Biomedical Sciences, College of Medicine, China Medical University, Taichung, 40402, Taiwan. achang68@mail.cmu.edu.tw.
Roswell Park Comprehensive Cancer Center · USCedars-Sinai Medical Center · USHarvard University · USIvy Tech Community College of Indiana · US

Funding

Two-Spirit Films in Indigenous Cancer HealthP30CA016056 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI Dean G. Tang · 1985 to 2026
$116.6M
Transgenic Mouse Core Facility Shared Resource (TMCF-SR)P30CA023168 · NCI · PURDUE UNIVERSITY WEST LAFAYETTE · PI Andrea L Kasinski · 1985 to 2026
$43.4M
NCI NIH HHS P30 CA016056NCI NIH HHS P30 CA023168
6 · The paper itself

Abstract

Epigenetic regulation plays an important role in governing stem cell fate and tumorigenesis. Lost expression of a key DNA demethylation enzyme TET2 is associated with human cancers and has been linked to stem cell traits in vitro; however, whether and how TET2 regulates mammary stem cell fate and mammary tumorigenesis in vivo remains to be determined. Here, using our recently established mammary specific Tet2 deletion mouse model, the data reveals that TET2 plays a pivotal role in mammary gland development and luminal lineage commitment. We show that TET2 and FOXP1 form a chromatin complex that mediates demethylation of ESR1, GATA3, and FOXA1, three key genes that are known to coordinately orchestrate mammary luminal lineage specification and endocrine response, and also are often silenced by DNA methylation in aggressive breast cancers. Furthermore, Tet2 deletion-PyMT breast cancer mouse model exhibits enhanced mammary tumor development with deficient ERα expression that confers tamoxifen resistance in vivo. As a result, this study elucidates a role for TET2 in governing luminal cell differentiation and endocrine response that underlies breast cancer resistance to anti-estrogen treatments.

Indexed as

Cell DifferentiationAnimalsBreast NeoplasmsCell LineageDioxygenasesDNA-Binding ProteinsDNA MethylationEndocrine SystemEpigenesis, GeneticEstradiolEstrogen Receptor alphaEstrogensFemaleHumansMammary Glands, AnimalMiceDioxygenasesDNA-Binding ProteinsEstradiolEstrogen Receptor alphaEstrogensProto-Oncogene ProteinsTet2 protein, mouse

Identifiers

PMID32934200
PMCPMC7493981
OpenAlexW3087589406

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.