Evidence map›Paper›PMID 35107765›Full record

ReviewCurrent atherosclerosis reports2022

SR-B1's Next Top Model: Structural Perspectives on the Functions of the HDL Receptor.

Hayley R Powers, Daisy Sahoo

Open access · bronzeAbstract readReview
In one paragraph

Review in Current atherosclerosis reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
6.8field-weighted citation impact, top 2% 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

15 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Improving Lipid Profiles ThroughFoods (Basel, Switzerland) · 2026
    Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Review
  12. New Insights on the Uptake and Trafficking of Coenzyme Q.Antioxidants (Basel, Switzerland) · 2023
    Review
  13. Article
  14. Review
  15. 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

2 authors at 1 institution in 1 country.

Hayley R PowersDepartment of Biochemistry, Medical College of Wisconsin, Milwaukee, WI, USA.
Daisy SahooDepartment of Biochemistry, Medical College of Wisconsin, Milwaukee, WI, USA. dsahoo@mcw.edu.ORCID 0000-0001-5210-6497
Medical College of Wisconsin · US

Funding

Selective Uptake and Hydrolysis of Cholesteryl Ester by SR-BIR01HL058012 · NHLBI · STATE UNIVERSITY NEW YORK STONY BROOK · PI SAHOO, DAISY · 1997 to 2023
$8.6M
Medical Scientist Training ProgramT32GM080202 · NIGMS · MEDICAL COLLEGE OF WISCONSIN · PI BARBIERI, JOSEPH T, SALZMAN, NITA H · 2010 to 2024
$5.7M
SR-BI and PCPE2: Novel partners in bi-directional cholesterol transportR01HL138907 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI SAHOO, DAISY, SORCI-THOMAS, MARY G · 2018 to 2021
$2.8M
Chronic gammaherpesvirus infection and high cholesterol: Adding fuel to the fireR21AI147500 · NIAID · MEDICAL COLLEGE OF WISCONSIN · PI SAHOO, DAISY, TARAKANOVA, VERA L. · 2020 to 2021
$424k
Identification of structural features of SR-BI that facilitate HDL-cholesterol clearanceF30HL151048 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI POWERS, HAYLEY R · 2020 to 2022
$145k
NHLBI NIH HHS F30 HL151048NHLBI NIH HHS R01 HL058012NHLBI NIH HHS R01 HL138907NIAID NIH HHS R21 AI147500NIGMS NIH HHS T32 GM080202
6 · The paper itself

Abstract

purpose of reviewThe binding of high-density lipoprotein (HDL) to its primary receptor, scavenger receptor class B type 1 (SR-B1), is critical for lowering plasma cholesterol levels and reducing cardiovascular disease risk. This review provides novel insights into how the structural elements of SR-B1 drive efficient function with an emphasis on bidirectional cholesterol transport. RECENT

findingsWe have generated a new homology model of full-length human SR-B1 based on the recent resolution of the partial structures of other class B scavenger receptors. Interrogating this model against previously published observations allows us to generate structurally informed hypotheses about SR-B1's ability to mediate HDL-cholesterol (HDL-C) transport. Furthermore, we provide a structural perspective as to why human variants of SR-B1 may result in impaired HDL-C clearance. A comprehensive understanding of SR-B1's structure-function relationships is critical to the development of therapeutic agents targeting SR-B1 and modulating cardiovascular disease risk.

Indexed as

Cardiovascular DiseasesCholesterol, HDLHumansLipoproteins, HDLReceptors, LipoproteinScavenger Receptors, Class BCholesterol, HDLhigh density lipoprotein receptorsLipoproteins, HDLReceptors, LipoproteinScavenger Receptors, Class BCardiovascular diseaseCholesterolHigh-density lipoproteinOligomerizationScavenger receptor class B type 1Structural biology

Identifiers

PMID35107765
PMCPMC8809234
OpenAlexW4210358347

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.