Evidence map›Paper›PMID 33539963›Full record

ReviewMolecular and cellular endocrinology2021

Long noncoding RNAs-a new dimension in the molecular architecture of the bile acid/FXR pathway.

Yonghe Ma, Jamie Harris, Ping Li, Haiming Cao

Open access · greenAbstract readReview
In one paragraph

Review in Molecular and cellular endocrinology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 54% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Article
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

4 authors at 1 institution in 1 country.

Yonghe MaCardiovascular Branch, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, MD, 20892, USA.
Jamie HarrisCardiovascular Branch, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, MD, 20892, USA.
Ping LiCardiovascular Branch, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, MD, 20892, USA.
Haiming CaoCardiovascular Branch, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, MD, 20892, USA. Electronic address: haiming.cao@nih.gov.
National Institutes of Health · US

Funding

Molecular Basis of Obesity and Obesity-induced Metabolic DiseasesZIAHL006103 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI CAO, HAIMING · 2011 to 2025
$19.8M
Modeling Type II Diabetes and Lipodystrophy Using Patient-Specific iPS CellsZIAHL006159 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI CAO, HAIMING · 2012 to 2025
$14.2M
Intramural NIH HHS ZIA HL006103Intramural NIH HHS ZIA HL006159
6 · The paper itself

Abstract

Bile acids, regarded as the body's detergent for digesting lipids, also function as critical signaling molecules that regulate cholesterol and triglyceride levels in the body. Bile acids are the natural ligands of the nuclear receptor, FXR, which controls an intricate network of cellular pathways to maintain metabolic homeostasis. In recent years, growing evidence supports that many cellular actions of the bile acid/FXR pathway are mediated by long non-coding RNAs (lncRNAs), and lncRNAs are in turn powerful regulators of bile acid levels and FXR activities. In this review, we highlight the substantial progress made in the understanding of the functional and mechanistic role of lncRNAs in bile acid metabolism and how lncRNAs connect bile acid activity to additional metabolic processes. We also discuss the potential of lncRNA studies in elucidating novel molecular mechanisms of the bile acid/FXR pathway and the promise of lncRNAs as potential diagnostic markers and therapeutic targets for diseases associated with altered bile acid metabolism.

Indexed as

Signal TransductionAnimalsBile Acids and SaltsDiseaseHumansLiverReceptor, Farnesoid X-ActivatedReceptors, Cytoplasmic and NuclearRNA, Long NoncodingBile Acids and SaltsReceptor, Farnesoid X-ActivatedReceptors, Cytoplasmic and NuclearRNA, Long Noncoding

Identifiers

PMID33539963
PMCPMC8437140
OpenAlexW3127480450

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.