Evidence map›Paper›PMID 33390931›Full record

ArticleFrontiers in pharmacology2020

Synergetic Effect of rHDL and LXR Agonist on Reduction of Atherosclerosis in Mice.

Emily E Morin, Yanhong Guo, Hongliang He, Wenmin Yuan, Whitney N Souery, Maria V Fawaz, Yuqing Eugene Chen, Anna Schwendeman

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.0field-weighted citation impact, top 12% 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

4 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Molecules (Basel, Switzerland) · 2022
    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

8 authors at 3 institutions in 1 country.

Emily E MorinDepartment of Pharmaceutical Sciences, University of Michigan, Ann Arbor, MI, United States.
Yanhong GuoDepartment of Internal Medicine, University of Michigan, NCRC, Ann Arbor, MI, United States.
Hongliang HeDepartment of Pharmaceutical Sciences, University of Michigan, Ann Arbor, MI, United States.
Wenmin YuanDepartment of Pharmaceutical Sciences, University of Michigan, Ann Arbor, MI, United States.
Whitney N SoueryDepartment of Pharmaceutical Sciences, University of Michigan, Ann Arbor, MI, United States.
Maria V FawazDepartment of Medicinal Chemistry, University of Michigan, Ann Arbor, MI, United States.
Yuqing Eugene ChenDepartment of Internal Medicine, University of Michigan, NCRC, Ann Arbor, MI, United States.
Anna SchwendemanDepartment of Pharmaceutical Sciences, University of Michigan, Ann Arbor, MI, United States.
University of Michigan–Ann Arbor · USMichigan Cancer Research Consortium · USBioSurfaces (United States) · US

Funding

WOMEN'S CANCERS RESEARCH PROGRAMP30CA118100 · NCI · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI Yolanda Sanchez · 2005 to 2026
$57.1M
FAIR Data Competency and Machine Learning Readiness for Biomedical ScientistsK12GM088021 · NIGMS · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI REBECCA S. HARTLEY, Diane Lidke · 2009 to 2026
$16.4M
NCI NIH HHS P30 CA118100NIGMS NIH HHS K12 GM088021
6 · The paper itself

Abstract

High-density lipoproteins (HDLs) are unique in that they play an important role in the reverse cholesterol transport process. However, reconstituted HDL (rHDL) infusions have demonstrated limited beneficial effect in clinical practice. This is perhaps a consequence of the limited cholesterol efflux abilities of atheroma macrophages due to decreased expression of cholesterol transporters in advanced atheromas and following rHDL infusion treatment. Thus, we propose that a combination therapy of rHDL and a liver X receptor (LXR) agonist could maximize the therapeutic benefit of rHDL by upregulating ATP-binding cassette transporters A-1 (ABCA1) and ATP-binding cassette transporter G-1 (ABCG1), and enhancing cholesterol efflux to rHDL. In macrophages, rHDL downregulated the expression of ABCA1/G1 in a dose- and rHDL composition-dependent manner. Although LXR agonist, T0901317 (T1317), upregulated the expression of ABCA1 and ABCG1, the drug itself did not have any effect on cholesterol efflux (6.6 ± 0.5%) while the combination of rHDL and T1317 exhibited enhanced cholesterol efflux from [

Indexed as

atherosclerosischolesterol effluxcoronary artery diseasehigh-density lipoproteinliver X receptor

Identifiers

PMID33390931
PMCPMC7772318
OpenAlexW3112413966

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.