Evidence map›Paper›PMID 36399508›Full record

ArticleNucleic acids research2022

Glucocorticoids unmask silent non-coding genetic risk variants for common diseases.

Thanh Thanh L Nguyen, Huanyao Gao, Duan Liu, Trudy Janice Philips, Zhenqing Ye, Jeong-Heon Lee, Geng-Xian Shi, Kaleigh Copenhaver, Lingxin Zhang, Lixuan Wei and 10 more

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

9 citing papers in PubMed, 11 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

20 authors at 3 institutions in 1 country.

Thanh Thanh L NguyenDepartment of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic; Rochester, MN, USA.ORCID 0000-0002-2281-6540
Huanyao GaoDepartment of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic; Rochester, MN, USA.
Duan LiuDepartment of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic; Rochester, MN, USA.ORCID 0000-0003-1065-246X
Trudy Janice PhilipsDepartment of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic; Rochester, MN, USA.
Zhenqing YeDepartment of Health Sciences Research, Mayo Clinic; Rochester, MN, USA.
Jeong-Heon LeeEpigenomics Program, Center for Individualized Medicine, Mayo Clinic; Rochester, MN, USA.
Geng-Xian ShiEpigenomics Program, Center for Individualized Medicine, Mayo Clinic; Rochester, MN, USA.
Kaleigh CopenhaverDepartment of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic; Rochester, MN, USA.
Lingxin ZhangDepartment of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic; Rochester, MN, USA.ORCID 0000-0001-7068-7168
Lixuan WeiDepartment of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic; Rochester, MN, USA.
Jia YuDepartment of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic; Rochester, MN, USA.
Huan ZhangDepartment of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic; Rochester, MN, USA.ORCID 0000-0002-3968-6463
Abhijeet BarathDepartment of Neuroscience, Mayo Clinic; Rochester, MN, USA.
Maggie LuongDepartment of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic; Rochester, MN, USA.
Cheng ZhangDepartment of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic; Rochester, MN, USA.ORCID 0000-0003-3843-1562
Alexandre Gaspar-MaiaEpigenomics Program, Center for Individualized Medicine, Mayo Clinic; Rochester, MN, USA.
Hu LiDepartment of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic; Rochester, MN, USA.
Liewei WangDepartment of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic; Rochester, MN, USA.
Tamas OrdogEpigenomics Program, Center for Individualized Medicine, Mayo Clinic; Rochester, MN, USA.
Richard M WeinshilboumDepartment of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic; Rochester, MN, USA.
Mayo Clinic · USThe University of Texas Health Science Center at San Antonio · USUniversity of Minnesota Rochester · US

Funding

Women's Cancer ProgramP30CA015083 · NCI · MAYO CLINIC ROCHESTER · PI Lila J. Rutten · 1985 to 2026
$151.3M
Pharmacogenetics of Phase II Drug Metabolizing EnzymesU19GM061388 · NIGMS · MAYO CLINIC ROCHESTER · PI WEINSHILBOUM, RICHARD M. · 2010 to 2014
$15.8M
INHERITED VARIATIONS IN DRUG-METABOLIZING ENZYMESR01GM028157 · NIGMS · MAYO CLINIC ROCHESTER · PI WEINSHILBOUM, RICHARD M. · 1985 to 2019
$6.9M
Interstitial Cells of Cajal in Diabetic GastropathyR01DK058185 · NIDDK · UNIVERSITY OF NEVADA RENO · PI ORDOG, TAMAS · 2002 to 2020
$5.2M
Alcohol Use Disorder: Acamprosate Pharmacometabolomics-informed PharmacogenomicsR01AA027486 · NIAAA · MAYO CLINIC ROCHESTER · PI Ming-Fen Ho, Richard M. Weinshilboum · 2018 to 2026
$4.0M
Epigenetic dysregulation in diabetic enteric neuropathyR01DK126827 · NIDDK · MAYO CLINIC ROCHESTER · PI ORDOG, TAMAS · 2021 to 2024
$2.1M
NCI NIH HHS P30 CA015083NIAAA NIH HHS R01 AA027486NIDDK NIH HHS R01 DK058185NIDDK NIH HHS R01 DK126827NIGMS NIH HHS R01 GM028157NIGMS NIH HHS U19 GM061388
6 · The paper itself

Abstract

Understanding the function of non-coding genomic sequence variants represents a challenge for biomedicine. Many diseases are products of gene-by-environment interactions with complex mechanisms. This study addresses these themes by mechanistic characterization of non-coding variants that influence gene expression only after drug or hormone exposure. Using glucocorticoid signaling as a model system, we integrated genomic, transcriptomic, and epigenomic approaches to unravel mechanisms by which variant function could be revealed by hormones or drugs. Specifically, we identified cis-regulatory elements and 3D interactions underlying ligand-dependent associations between variants and gene expression. One-quarter of the glucocorticoid-modulated variants that we identified had already been associated with clinical phenotypes. However, their affected genes were 'unmasked' only after glucocorticoid exposure and often with function relevant to the disease phenotypes. These diseases involved glucocorticoids as risk factors or therapeutic agents and included autoimmunity, metabolic and mood disorders, osteoporosis and cancer. For example, we identified a novel breast cancer risk gene, MAST4, with expression that was repressed by glucocorticoids in cells carrying the risk genotype, repression that correlated with MAST4 expression in breast cancer and treatment outcomes. These observations provide a mechanistic framework for understanding non-coding genetic variant-chemical environment interactions and their role in disease risk and drug response.

Indexed as

GlucocorticoidsRegulatory Sequences, Nucleic AcidHumansPharmacogeneticsQuantitative Trait LociRisk FactorsGlucocorticoids

Identifiers

PMID36399508
PMCPMC9723631
OpenAlexW4309306014

What OpenQuestion holds

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Registered trials

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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.