Evidence map›Paper›PMID 27432117›Full record

ArticleJournal of biological rhythms2016

Genetic and Environmental Models of Circadian Disruption Link SRC-2 Function to Hepatic Pathology.

Tiffany Fleet, Erin Stashi, Bokai Zhu, Kimal Rajapakshe, Kathrina L Marcelo, Nicole M Kettner, Blythe K Gorman, Cristian Coarfa, Loning Fu, Bert W O'Malley and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of biological rhythms, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
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  10. SRC-2 Coactivator: a role in human metabolic evolution and disease.Molecular medicine (Cambridge, Mass.) · 2020
    Article
  11. Review
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  15. Precision medicine in alcoholic and nonalcoholic fatty liver disease via modulating the gut microbiota.American journal of physiology. Gastrointestinal and liver physiology · 2016
    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

11 authors at 3 institutions in 1 country.

Tiffany FleetInterdepartmental Department in Translational Biology and Molecular Medicine, Baylor College of Medicine, Houston, Texas.
Erin StashiDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas.
Bokai ZhuDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas.
Kimal RajapaksheDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas.
Kathrina L MarceloDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas.
Nicole M KettnerDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas.
Blythe K GormanDepartment of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas Weill Medical College, Cornell University, New York, New York.
Cristian CoarfaDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas.
Loning FuDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas.
Bert W O'MalleyDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas Dan L. Duncan Cancer Center, Baylor College of Medicine, Houston, Texas york@bcm.edu.
Brian YorkDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas Dan L. Duncan Cancer Center, Baylor College of Medicine, Houston, Texas york@bcm.edu.
Baylor College of Medicine · USChildren's Cancer Center · USCornell University · US

Funding

ProteomicsU19DK062434 · NIDDK · UNIVERSITY OF TEXAS SW MED CTR/DALLAS · PI MANGELSDORF, DAVID J · 2002 to 2011
$37.4M
TISSUE COACTIVATOR AND RECEPTOR EXPRESSION FINGERPRINTSP01DK059820 · NIDDK · INSTITUT DE GENETIQUE ET BIOLOGIE MOLECU · PI O'MALLEY, BERT W · 2001 to 2016
$23.1M
REPRODUCTIVE HORMONES: BIOLOGICAL AND MOLECULAR ACTIONSR01HD008188 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI DAVID M LONARD, JOHN P LYDON · 1985 to 2026
$16.3M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM007330 · NIGMS · BAYLOR COLLEGE OF MEDICINE · PI PLON, SHARON E. · 1985 to 2019
$15.6M
Diabetes Endocrinology Research CenterP30DK079638 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI CHAN, LAWRENCE · 2008 to 2012
$6.4M
STRUCTURE/FUNCTION OF GENETIC ENGINEERED CALMODULINSR01GM033976 · NIGMS · DUKE UNIVERSITY · PI MEANS, ANTHONY R · 1985 to 2015
$5.4M
The Study of the Circadian Rhythm in p53 SignalingR01CA137019 · NCI · BAYLOR COLLEGE OF MEDICINE · PI FU, LONING NONE · 2010 to 2014
$1.5M
Steroid Receptor Coactivator-2 as a key hepatic tumor suppressor and circadian meF31CA171350 · NCI · BAYLOR COLLEGE OF MEDICINE · PI STASHI, ERIN · 2012 to 2014
$119k
SRC-2 and AMPKa2 in liver metabolism and Non-Alcoholic Fatty Liver DiseaseF31DK107254 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI FLEET, TIFFANY C. · 2016 to 2017
$88k
NCI NIH HHS F31 CA171350NCI NIH HHS R01 CA137019NICHD NIH HHS R01 HD008188NIDDK NIH HHS F31 DK107254NIDDK NIH HHS P01 DK059820NIDDK NIH HHS P30 DK079638NIDDK NIH HHS U19 DK062434NIGMS NIH HHS R01 GM033976NIGMS NIH HHS T32 GM007330
6 · The paper itself

Abstract

Circadian rhythmicity is a fundamental process that synchronizes behavioral cues with metabolic homeostasis. Disruption of daily cycles due to jet lag or shift work results in severe physiological consequences including advanced aging, metabolic syndrome, and even cancer. Our understanding of the molecular clock, which is regulated by intricate positive feedforward and negative feedback loops, has expanded to include an important metabolic transcriptional coregulator, Steroid Receptor Coactivator-2 (SRC-2), that regulates both the central clock of the suprachiasmatic nucleus (SCN) and peripheral clocks including the liver. We hypothesized that an environmental uncoupling of the light-dark phases, termed chronic circadian disruption (CCD), would lead to pathology similar to the genetic circadian disruption observed with loss of SRC-2 We found that CCD and ablation of SRC-2 in mice led to a common comorbidity of metabolic syndrome also found in humans with circadian disruption, non-alcoholic fatty liver disease (NAFLD). The combination of SRC-2(-/-) and CCD results in a more robust phenotype that correlates with human non-alcoholic steatohepatitis (NASH) and hepatocellular carcinoma (HCC) gene signatures. Either CCD or SRC-2 ablation produces an advanced aging phenotype leading to increased mortality consistent with other circadian mutant mouse models. Collectively, our studies demonstrate that SRC-2 provides an essential link between the behavioral activities influenced by light cues and the metabolic homeostasis maintained by the liver.

Indexed as

AgingAnimalsCarcinoma, HepatocellularCircadian ClocksCircadian RhythmDisease Models, AnimalHumansLiverLiver NeoplasmsMiceNon-alcoholic Fatty Liver DiseaseNuclear Receptor Coactivator 2Period Circadian ProteinsPhotoperiodSuprachiasmatic NucleusNuclear Receptor Coactivator 2Period Circadian Proteinschronic circadian disruptionlivermetabolismNAFLDnon-alcoholic fatty liver diseaseSRC-2

Identifiers

PMID27432117
PMCPMC5248931
OpenAlexW2505255885

What OpenQuestion holds

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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.