Evidence map›Paper›PMID 30360449›Full record

ReviewInternational journal of molecular sciences2018

Novel Transcriptional Mechanisms for Regulating Metabolism by Thyroid Hormone.

Brijesh Kumar Singh, Rohit Anthony Sinha, Paul Michael Yen

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
3.4field-weighted citation impact, top 6% 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, 1 synthesis or guideline pooled it, 49 citations in OpenAlex.

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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

3 authors at 3 institutions in 3 countries.

Brijesh Kumar SinghLaboratory of Hormonal Regulation, Cardiovascular and Metabolic Disorders Program, Duke-NUS Medical School, Singapore 169857, Singapore. singhbrijeshk@duke-nus.edu.sg.ORCID 0000-0003-4615-3988
Rohit Anthony SinhaDepartment of Endocrinology, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Raebareli Road, Lucknow 226014, Uttar Pradesh, India. anthony.rohit@gmail.com.
Paul Michael YenLaboratory of Hormonal Regulation, Cardiovascular and Metabolic Disorders Program, Duke-NUS Medical School, Singapore 169857, Singapore. paul.yen@duke-nus.edu.sg.
Duke-NUS Medical School · SGDuke University · USSanjay Gandhi Post Graduate Institute of Medical Sciences · IN

Funding

DBT India Alliance IA/I/16/2/502691National Medical Research Council CIRG/1340/2012National Medical Research Council NMRC/CSA Grant/MH95:03/1-8National Medical Research Council NMRC/OFYIRG/0002/2016
6 · The paper itself

Abstract

The thyroid hormone plays a key role in energy and nutrient metabolisms in many tissues and regulates the transcription of key genes in metabolic pathways. It has long been believed that thyroid hormones (THs) exerted their effects primarily by binding to nuclear TH receptors (THRs) that are associated with conserved thyroid hormone response elements (TREs) located on the promoters of target genes. However, recent transcriptome and ChIP-Seq studies have challenged this conventional view as discordance was observed between TH-responsive genes and THR binding to DNA. While THR association with other transcription factors bound to DNA, TH activation of THRs to mediate effects that do not involve DNA-binding, or TH binding to proteins other than THRs have been invoked as potential mechanisms to explain this discrepancy, it appears that additional novel mechanisms may enable TH to regulate the mRNA expression. These include activation of transcription factors by SIRT1 via metabolic actions by TH, the post-translational modification of THR, the THR co-regulation of transcription with other nuclear receptors and transcription factors, and the microRNA (miR) control of RNA transcript expression to encode proteins involved in the cellular metabolism. Together, these novel mechanisms enlarge and diversify the panoply of metabolic genes that can be regulated by TH.

Indexed as

AnimalsERRalpha Estrogen-Related ReceptorForkhead Box Protein O1HumansLipid MetabolismMicroRNAsNon-alcoholic Fatty Liver DiseaseReceptors, EstrogenThyroid HormonesERRalpha Estrogen-Related ReceptorForkhead Box Protein O1MicroRNAsReceptors, EstrogenThyroid Hormonesestrogen-related receptor alpha (ERRαforkhead box protein O1 (FOXO1)gene transcriptionlipid metabolismmetabolismmicroRNAsmicroRNAs (miRs)non-alcoholic fatty liver disease (NAFLD)SIRT1thyroid hormone

Identifiers

PMID30360449
PMCPMC6214012
OpenAlexW2896887402

What OpenQuestion holds

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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.