Evidence map›Paper›PMID 24729624›Full record

ArticleJournal of lipid research2014

RNA binding protein HuR regulates the expression of ABCA1.

Cristina M Ramírez, Chin Sheng Lin, Kotb Abdelmohsen, Leigh Goedeke, Je-Hyun Yoon, Julio Madrigal-Matute, Jose L Martin-Ventura, Dat T Vo, Philip J Uren, Luiz O Penalva and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of lipid research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

26 citing papers in PubMed, 44 citations in OpenAlex.

  1. Review
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  11. ABCA1, ABCG1, and Cholesterol Homeostasis.Advances in experimental medicine and biology · 2022
    Article
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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

12 authors at 8 institutions in 3 countries.

Cristina M RamírezVascular Biology and Therapeutics Program, Department of Comparative Medicine, Yale University School of Medicine, New Haven, CT 06520 Departments of Medicine and Cell Biology, New York University School of Medicine, New York, NY 10016.
Chin Sheng LinDepartments of Medicine and Cell Biology, New York University School of Medicine, New York, NY 10016 Division of Cardiology, Department of Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan, Republic of China.
Kotb AbdelmohsenLaboratory of Genetics, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224.
Leigh GoedekeVascular Biology and Therapeutics Program, Department of Comparative Medicine, Yale University School of Medicine, New Haven, CT 06520 Departments of Medicine and Cell Biology, New York University School of Medicine, New York, NY 10016.
Je-Hyun YoonLaboratory of Genetics, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224.
Julio Madrigal-MatuteDepartments of Medicine and Cell Biology, New York University School of Medicine, New York, NY 10016.
Jose L Martin-VenturaVascular Research Lab, IIS-Fundación Jimenez Díaz, Autónoma University, Madrid 28040, Spain.
Dat T VoChildren's Cancer Research Institute, Department of Cellular and Structural Biology, University of Texas Health Science Center at San Antonio, San Antonio, TX 78229.
Philip J UrenMolecular and Computational Biology, University of Southern California, Los Angeles, CA 90089.
Luiz O PenalvaChildren's Cancer Research Institute, Department of Cellular and Structural Biology, University of Texas Health Science Center at San Antonio, San Antonio, TX 78229.
Myriam GorospeLaboratory of Genetics, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224.
Carlos Fernández-HernandoVascular Biology and Therapeutics Program, Department of Comparative Medicine, Yale University School of Medicine, New Haven, CT 06520 Departments of Medicine and Cell Biology, New York University School of Medicine, New York, NY 10016.
New York University · USNational Institutes of Health · USCancer Research Institute · USHospital Universitario Fundación Jiménez Díaz · ESNational Institute on Aging · USThe University of Texas Health Science Center at San Antonio · USUniversity of Southern California · USYale University · US

Funding

Post-transcriptional regulation of energy usage: glucose and lipid metabolismZIAAG000394 · NIA · NATIONAL INSTITUTE ON AGING · PI GOROSPE, MYRIAM · 2009 to 2025
$18.7M
Caveolin-1 in Lipoprotein Metabolism and Atherosclerosis.R01HL106063 · NHLBI · YALE UNIVERSITY · PI FERNANDEZ HERNANDO, CARLOS · 2011 to 2016
$2.5M
Role of microRNAs in lipid metabolism and cardiovascular diseaseR01HL107953 · NHLBI · YALE UNIVERSITY · PI FERNANDEZ HERNANDO, CARLOS · 2011 to 2016
$2.4M
MiR-33 and Aging: Implications for Metabolic SyndromeF31AG043318 · NIA · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI GOEDEKE, LEIGH · 2012 to 2014
$125k
NHLBI NIH HHS R01 HL106063NHLBI NIH HHS R01 HL107953NIA NIH HHS F31 AG043318
6 · The paper itself

Abstract

ABCA1 is a major regulator of cellular cholesterol efflux and plasma HDL biogenesis. Even though the transcriptional activation of ABCA1 is well established, the posttranscriptional regulation of ABCA1 expression is poorly understood. Here, we investigate the potential contribution of the RNA binding protein (RBP) human antigen R (HuR) on the posttranscriptional regulation of ABCA1 expression. RNA immunoprecipitation assays demonstrate a direct interaction between HuR and ABCA1 mRNA. We found that HuR binds to the 3' untranslated region of ABCA1 and increases ABCA1 translation, while HuR silencing reduces ABCA1 expression and cholesterol efflux to ApoA1 in human hepatic (Huh-7) and monocytic (THP-1) cells. Interestingly, cellular cholesterol levels regulate the expression, intracellular localization, and interaction between HuR and ABCA1 mRNA. Finally, we found that HuR expression was significantly increased in macrophages from human atherosclerotic plaques, suggesting an important role for this RBP in controlling macrophage cholesterol metabolism in vivo. In summary, we have identified HuR as a novel posttranscriptional regulator of ABCA1 expression and cellular cholesterol homeostasis, thereby opening new avenues for increasing cholesterol efflux from atherosclerotic foam macrophages and raising circulat-ing HDL cholesterol levels.

Indexed as

Gene Expression RegulationApolipoprotein A-IAtherosclerosisATP Binding Cassette Transporter 1CholesterolELAV-Like Protein 1Foam CellsHomeostasisHumansRNA, MessengerTHP-1 CellsABCA1 protein, humanAPOA1 protein, humanApolipoprotein A-IATP Binding Cassette Transporter 1CholesterolELAVL1 protein, humanELAV-Like Protein 1RNA, MessengerATP binding cassette transporter A1cholesterol effluxhuman antigen Rlipid homeostasisposttranscriptional regulation

Identifiers

PMID24729624
PMCPMC4031938
OpenAlexW2099938245

What OpenQuestion holds

Textmetadata
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.