Evidence map›Paper›PMID 22935699›Full record

ArticleCell cycle (Georgetown, Tex.)2012

Identification of an estrogen-regulated circadian mechanism necessary for breast acinar morphogenesis.

Stefano Rossetti, Francesca Corlazzoli, Alex Gregorski, Nurul Hidayah A Azmi, Nicoletta Sacchi

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
0.5field-weighted citation impact, top 43% 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

25 citing papers in PubMed, 66 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Estrogens and the circadian system.Seminars in cell & developmental biology · 2022
    Review
  11. Article
  12. Review
  13. Review
  14. MYC-Associated Factor MAX is a Regulator of the Circadian Clock.International journal of molecular sciences · 2020
    Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. The sweet tooth of the circadian clock.Biochemical Society transactions · 2017
    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 2 institutions in 1 country.

Stefano RossettiDepartment of Cancer Genetics, Roswell Park Cancer Institute, Buffalo, NY, USA.
Francesca Corlazzoli
Alex Gregorski
Nurul Hidayah A Azmi
Nicoletta Sacchi
Cancer Genetics (United States) · USRoswell Park Comprehensive Cancer Center · US

Funding

Two-Spirit Films in Indigenous Cancer HealthP30CA016056 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI MARK G FRATTINI · 1985 to 2026
$116.6M
NCI NIH HHS P30 CA016056
6 · The paper itself

Abstract

Altered estrogen receptor α (ERA) signaling and altered circadian rhythms are both features of breast cancer. By using a method to entrain circadian oscillations in human cultured cells, we recently reported that the expression of key clock genes oscillates in a circadian fashion in ERA-positive breast epithelial cells but not in breast cancer cells, regardless of their ERA status. Moreover, we reported that ERA mRNA oscillates in a circadian fashion in ERA-positive breast epithelial cells, but not in ERA-positive breast cancer cells. By using ERA-positive HME1 breast epithelial cells, which can be both entrained in vitro and can form mammary gland-like acinar structures in three-dimensional (3D) culture, first we identified a circuit encompassing ERA and an estrogen-regulated loop consisting of two circadian clock genes, PER2 and BMAL1. Further, we demonstrated that this estrogen-regulated circuit is necessary for breast epithelial acinar morphogenesis. Disruption of this circuit due to ERA-knockdown, negatively affects the estrogen-sustained circadian PER2-BMAL1 mechanism as well as the formation of 3D HME1 acini. Conversely, knockdown of either PER2 or BMAL1, by hampering the PER2-BMAL1 loop of the circadian clock, negatively affects ERA circadian oscillations and 3D breast acinar morphogenesis. To our knowledge, this study provides the first evidence of the implication of an ERA-circadian clock mechanism in the breast acinar morphogenetic process.

Indexed as

Acinar CellsARNTL Transcription FactorsBreastCircadian RhythmDown-RegulationEstrogen Receptor alphaEstrogensFemaleGene Knockdown TechniquesHumansModels, BiologicalMorphogenesisPeriod Circadian ProteinsRNA, MessengerTranscription, GeneticARNTL Transcription FactorsBMAL1 protein, humanESR1 protein, humanEstrogen Receptor alphaEstrogensPER2 protein, humanPeriod Circadian ProteinsRNA, Messenger

Identifiers

PMID22935699
PMCPMC3478319
OpenAlexW2017333590

What OpenQuestion holds

Textmetadata
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.