Evidence map›Paper›PMID 31291759›Full record

ArticleArteriosclerosis, thrombosis, and vascular biology2019

Hepatic Forkhead Box Protein A3 Regulates ApoA-I (Apolipoprotein A-I) Expression, Cholesterol Efflux, and Atherogenesis.

Yuanyuan Li, Yanyong Xu, Kavita Jadhav, Yingdong Zhu, Liya Yin, Yanqiao Zhang

Open access · bronzeAbstract read
In one paragraph

Article in Arteriosclerosis, thrombosis, and vascular biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

21 citing papers in PubMed, 31 citations in OpenAlex.

  1. Veterinary sciences · 2026
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  12. Biomolecules · 2022
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  13. HDL and ASCVD.Advances in experimental medicine and biology · 2022
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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

6 authors at 1 institution in 1 country.

Yuanyuan LiFrom the Department of Integrative Medical Sciences, Northeast Ohio Medical University, Rootstown.
Yanyong XuFrom the Department of Integrative Medical Sciences, Northeast Ohio Medical University, Rootstown.
Kavita JadhavFrom the Department of Integrative Medical Sciences, Northeast Ohio Medical University, Rootstown.
Yingdong ZhuFrom the Department of Integrative Medical Sciences, Northeast Ohio Medical University, Rootstown.
Liya YinFrom the Department of Integrative Medical Sciences, Northeast Ohio Medical University, Rootstown.
Yanqiao ZhangFrom the Department of Integrative Medical Sciences, Northeast Ohio Medical University, Rootstown.
Northeast Ohio Medical University · US

Funding

Mechanisms Underlying the Pathogenesis of Non-alcoholic Fatty Liver DiseaseR01DK102619 · NIDDK · UNIVERSITY OF ARIZONA · PI Yanqiao Zhang · 2015 to 2026
$4.0M
Regulation of Lipid and Lipoprotein Metabolism by Nuclear ReceptorsR01HL103227 · NHLBI · NORTHEAST OHIO MEDICAL UNIVERSITY · PI YIN, LIYA, ZHANG, YANQIAO · 2011 to 2019
$3.1M
Identification of Novel Genes/Pathways That Regulate AtherogenesisR01HL142086 · NHLBI · NORTHEAST OHIO MEDICAL UNIVERSITY · PI ZHANG, YANQIAO · 2018 to 2021
$2.1M
Hepatic FOXA3 Links NAFLD to AtherosclerosisR01DK118805 · NIDDK · NORTHEAST OHIO MEDICAL UNIVERSITY · PI ZHANG, YANQIAO · 2019 to 2022
$2.0M
Identification of Novel Genes/Pathways That Regulate Lipid and Glucose MetabolismR01DK095895 · NIDDK · NORTHEAST OHIO MEDICAL UNIVERSITY · PI ZHANG, YANQIAO · 2012 to 2015
$1.3M
NHLBI NIH HHS R01 HL103227NHLBI NIH HHS R01 HL142086NIDDK NIH HHS R01 DK095895NIDDK NIH HHS R01 DK102619NIDDK NIH HHS R01 DK118805
6 · The paper itself

Abstract

objectiveTo determine the role of hepatic FOXA3 (forkhead box A3) in lipid metabolism and atherosclerosis. Approach and Results: Hepatic FOXA3 expression was reduced in diabetic or high fat diet-fed mice or patients with nonalcoholic steatohepatitis. We then used adenoviruses to overexpress or knock down hepatic FOXA3 expression. Overexpression of FOXA3 in the liver increased hepatic ApoA-I (apolipoprotein A-I) expression, plasma HDL-C (high-density lipoprotein cholesterol) level, macrophage cholesterol efflux, and macrophage reverse cholesterol transport. In contrast, knockdown of hepatic FOXA3 expression had opposite effects. We further showed that FOXA3 directly bound to the promoter of the Apoa1 gene to regulate its transcription. Finally, AAV8 (adeno-associated virus serotype 8)-mediated overexpression of human FOXA3 in the hepatocytes of Apoe

conclusionsHepatocyte FOXA3 protects against atherosclerosis by inducing ApoA-I and macrophage reverse cholesterol transport.

Indexed as

AnimalsApolipoprotein A-IAtherosclerosisBiological TransportCholesterolCholesterol, HDLFemaleHepatocyte Nuclear Factor 3-gammaHep G2 CellsHumansLiverMacrophagesMiceMice, Inbred C57BLApolipoprotein A-ICholesterolCholesterol, HDLFOXA3 protein, humanHepatocyte Nuclear Factor 3-gammaatherosclerosischolesterol effluxFOXA3livermacrophages

Identifiers

PMID31291759
PMCPMC6656627
OpenAlexW2961316843

What OpenQuestion holds

Textmetadata
LicenceTDM
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.