Evidence map›Paper›PMID 24759789›Full record

ArticleBiology of reproduction2014

Tissue-specific changes in molecular clocks during the transition from pregnancy to lactation in mice.

Theresa M Casey, Jennifer Crodian, Emily Erickson, Karen K Kuropatwinski, Anatoli S Gleiberman, Marina P Antoch

Open access · bronzeAbstract read
In one paragraph

Article in Biology of reproduction, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

23 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
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  12. Observational
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  15. Gestational disruptions in metabolic rhythmicity of the liver, muscle, and placenta affect fetal size.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2017
    Article
  16. Article
  17. CLOCK regulates mammary epithelial cell growth and differentiation.American journal of physiology. Regulatory, integrative and comparative physiology · 2016
    Article
  18. Circadian clocks and breast cancer.Breast cancer research : BCR · 2016
    Review
  19. Article
  20. 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

6 authors at 3 institutions in 1 country.

Theresa M CaseyDepartment of Animal Science, Purdue University, West Lafayette, Indiana theresa-casey@purdue.edu.
Jennifer CrodianDepartment of Animal Science, Purdue University, West Lafayette, Indiana.
Emily EricksonDepartment of Animal Science, Purdue University, West Lafayette, Indiana.
Karen K KuropatwinskiDepartment of Molecular and Cellular Biology, Roswell Park Cancer Institute, Buffalo, New York.
Anatoli S GleibermanCleveland BioLabs, Buffalo, New York.
Marina P AntochDepartment of Molecular and Cellular Biology, Roswell Park Cancer Institute, Buffalo, New York.
Purdue University West Lafayette · USRoswell Park Comprehensive Cancer Center · USCleveland BioLabs (United States) · US

Funding

Two-Spirit Films in Indigenous Cancer HealthP30CA016056 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI MARK G FRATTINI · 1985 to 2026
$116.6M
Engineering of Proteins for CrystallographyR01GM095847 · NIGMS · UNIVERSITY OF VIRGINIA · PI DEREWENDA, ZYGMUNT S, EISENBERG, DAVID · 2011 to 2014
$1.6M
An intercross between the circadian and NFkB pathwaysR01GM095874 · NIGMS · ROSWELL PARK CANCER INSTITUTE CORP · PI ANTOCH, MARINA, GUDKOV, ANDREI V · 2011 to 2014
$1.4M
Do circadian clocks coordinate physiological changes needed to initiate lactationR03HD062692 · NICHD · PURDUE UNIVERSITY · PI ANTOCH, MARINA, CASEY, THERESA MARIE · 2010 to 2010
$92k
NCI NIH HHS P30 CA016056NICHD NIH HHS 1R03HD062692-01A1NICHD NIH HHS R03 HD062692NIGMS NIH HHS GM095847NIGMS NIH HHS R01 GM095847NIGMS NIH HHS R01 GM095874
6 · The paper itself

Abstract

Circadian clocks regulate homeostasis and mediate responses to stressors. Lactation is one of the most energetically demanding periods of an adult female's life. Peripartum changes occur in almost every organ so the dam can support neonatal growth through milk production while homeostasis is maintained. How circadian clocks are involved in adaptation to lactation is currently unknown. The abundance and temporal pattern of core clock genes' expression were measured in suprachiasmatic nucleus, liver, and mammary from late pregnant and early lactation mice. Tissue-specific changes in molecular clocks occurred between physiological states. Amplitude and robustness of rhythms increased in suprachiasmatic nucleus and liver. Mammary rhythms of core molecular clock genes were suppressed. Attenuated rhythms appeared to be a physiological adaptation of mammary to lactation, because manipulation of timing of suckling resulting in significant differences in plasma prolactin and corticosterone had no effect on amplitude. Analysis of core clock proteins revealed that the stoichiometric relationship between positive (CLOCK) and negative (PER2) components remained 1:1 in liver but was increased to 4:1 in mammary during physiological transition. Induction of differentiation of mammary epithelial cell line HC11 with dexamethasone, insulin, and prolactin resulted in similar stoichiometric changes among positive and negative clock regulators, and prolactin induced phase shifts in HC11 Arntl expression rhythm. Data support that distinct mechanisms drive periparturient changes in mammary clock. Stoichiometric change in clock regulators occurs with gland differentiation. Suppression of mammary clock gene expression rhythms represents a physiological adaptation to suckling cues. Adaptations in mammary clock are likely needed in part to support suckling demands of neonates.

Indexed as

AnimalsARNTL Transcription FactorsBasic Helix-Loop-Helix ProteinsCell LineCircadian RhythmCircadian Rhythm Signaling Peptides and ProteinsCryptochromesEpithelial CellsFemaleLactationLiverMaleMammary Glands, AnimalMice, Inbred C57BLMilkNerve Tissue ProteinsARNTL Transcription FactorsBasic Helix-Loop-Helix ProteinsBmal1 protein, mouseCircadian Rhythm Signaling Peptides and ProteinsCry1 protein, mouseCry2 protein, mouseCryptochromesNerve Tissue ProteinsNpas2 protein, mousePer1 protein, mousePer2 protein, mousePer3 protein, mousePeriod Circadian Proteinscircadian clocklactationlivermammarypregnancyprolactinSCN

Identifiers

PMID24759789
PMCPMC4094001
OpenAlexW2138158893

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.