Evidence map›Paper›PMID 24987953›Full record

ReviewInternational journal of molecular sciences2014

Interplay between Dioxin-mediated signaling and circadian clock: a possible determinant in metabolic homeostasis.

Chun Wang, Zhi-Ming Zhang, Can-Xin Xu, Shelley A Tischkau

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 26% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Aryl hydrocarbon receptor activation alters emergency hematopoiesis during influenza A virus infection.Toxicological sciences : an official journal of the Society of Toxicology · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. The Landscape of AhR Regulators and Coregulators to Fine-Tune AhR Functions.International journal of molecular sciences · 2021
    Review
  10. Article
  11. Article
  12. Article
  13. 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

4 authors at 2 institutions in 2 countries.

Chun WangDepartment of Pharmacology, Southern Illinois University School of Medicine, Springfield, IL 62702, USA. cwang@siumed.edu.
Zhi-Ming ZhangDepartment of Anesthesiology, Institute of Translation Medicine, the First People's Hospital of Chenzhou, Chenzhou 423000, China. otc0735@gmail.com.
Can-Xin XuDepartment of Pharmacology, Southern Illinois University School of Medicine, Springfield, IL 62702, USA. cxu@siumed.edu.
Shelley A TischkauDepartment of Pharmacology, Southern Illinois University School of Medicine, Springfield, IL 62702, USA. stischkau@siumed.edu.
Southern Illinois University School of Medicine · USChenzhou First People's Hospital · CN

Funding

Circadian Clock Disruption: A Mechanism for Dioxin-induced Metabolic SyndromeR01ES017774 · NIEHS · SOUTHERN ILLINOIS UNIVERSITY SCH OF MED · PI TISCHKAU, SHELLEY A · 2010 to 2013
$1.3M
NIEHS NIH HHS ES01774NIEHS NIH HHS R01 ES017774
6 · The paper itself

Abstract

The rotation of the earth on its axis creates the environment of a 24 h solar day, which organisms on earth have used to their evolutionary advantage by integrating this timing information into their genetic make-up in the form of a circadian clock. This intrinsic molecular clock is pivotal for maintenance of synchronized homeostasis between the individual organism and the external environment to allow coordinated rhythmic physiological and behavioral function. Aryl hydrocarbon receptor (AhR) is a master regulator of dioxin-mediated toxic effects, and is, therefore, critical in maintaining adaptive responses through regulating the expression of phase I/II drug metabolism enzymes. AhR expression is robustly rhythmic, and physiological cross-talk between AhR signaling and circadian rhythms has been established. Increasing evidence raises a compelling argument that disruption of endogenous circadian rhythms contributes to the development of disease, including sleep disorders, metabolic disorders and cancers. Similarly, exposure to environmental pollutants through air, water and food, is increasingly cited as contributory to these same problems. Thus, a better understanding of interactions between AhR signaling and the circadian clock regulatory network can provide critical new insights into environmentally regulated disease processes. This review highlights recent advances in the understanding of the reciprocal interactions between dioxin-mediated AhR signaling and the circadian clock including how these pathways relate to health and disease, with emphasis on the control of metabolic function.

Indexed as

Circadian ClocksHomeostasisAnimalsDioxinsEnvironmental IllnessHumansReceptors, Aryl HydrocarbonSignal TransductionDioxinsReceptors, Aryl Hydrocarbon

Identifiers

PMID24987953
PMCPMC4139808
OpenAlexW1974545462

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.