Evidence map›Paper›PMID 25218443›Full record

ReviewThe Journal of steroid biochemistry and molecular biology2015

Acyl-CoA:cholesterol acyltransferases (ACATs/SOATs): Enzymes with multiple sterols as substrates and as activators.

Maximillian A Rogers, Jay Liu, Bao-Liang Song, Bo-Liang Li, Catherine C Y Chang, Ta-Yuan Chang

Open access · greenAbstract readReview
In one paragraph

Review in The Journal of steroid biochemistry and molecular biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed, 1 pooled it
6.2field-weighted citation impact, top 3% 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

75 citing papers in PubMed, 1 synthesis or guideline pooled it, 151 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Mechanism for oil-phase separation by the lipid droplet assembly complex.bioRxiv : the preprint server for biology · 2025
    Article
  6. Article
  7. Article
  8. mBio · 2025
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Enzymatically Formed Oxysterols and Cell Death.Advances in experimental medicine and biology · 2024
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review

15 more citing papers are in PubMed but not listed here.

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 4 institutions in 2 countries.

Maximillian A RogersDepartment of Biochemistry, Geisel School of Medicine, Dartmouth HB7200, Hanover, NH 03755, United States; Center for Interdisciplinary Cardiovascular Sciences, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, United States.
Jay LiuDepartment of Biochemistry, Geisel School of Medicine, Dartmouth HB7200, Hanover, NH 03755, United States.
Bao-Liang SongState Key Laboratory of Molecular Biology, Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, China.
Bo-Liang LiState Key Laboratory of Molecular Biology, Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, China.
Catherine C Y ChangDepartment of Biochemistry, Geisel School of Medicine, Dartmouth HB7200, Hanover, NH 03755, United States. Electronic address: Catherine.Chang@Dartmouth.Edu.
Ta-Yuan ChangDepartment of Biochemistry, Geisel School of Medicine, Dartmouth HB7200, Hanover, NH 03755, United States. Electronic address: ta.yuan.chang@dartmouth.edu.
Dartmouth College · USBrigham and Women's Hospital · USCenter for Excellence in Molecular Cell Science · CNChinese Academy of Sciences · CN

Funding

STRUCTURE/FUNCTION ANALYSIS OF ACATR01HL060306 · NHLBI · DARTMOUTH COLLEGE · PI CHANG, TA YUAN · 1998 to 2015
$5.5M
Impact of microglial cholesterol storage on neuroinflammationR01AG037609 · NIA · DARTMOUTH COLLEGE · PI CHANG, TA YUAN · 2010 to 2019
$3.3M
NHLBI NIH HHS HL 60306NHLBI NIH HHS R01 HL060306NIA NIH HHS AG37609NIA NIH HHS R01 AG037609
6 · The paper itself

Abstract

Cholesterol is essential to the growth and viability of cells. The metabolites of cholesterol include: steroids, oxysterols, and bile acids, all of which play important physiological functions. Cholesterol and its metabolites have been implicated in the pathogenesis of multiple human diseases, including: atherosclerosis, cancer, neurodegenerative diseases, and diabetes. Thus, understanding how cells maintain the homeostasis of cholesterol and its metabolites is an important area of study. Acyl-coenzyme A:cholesterol acyltransferases (ACATs, also abbreviated as SOATs) converts cholesterol to cholesteryl esters and play key roles in the regulation of cellular cholesterol homeostasis. ACATs are most unusual enzymes because (i) they metabolize diverse substrates including both sterols and certain steroids; (ii) they contain two different binding sites for steroidal molecules. In mammals, there are two ACAT genes that encode two different enzymes, ACAT1 and ACAT2. Both are allosteric enzymes that can be activated by a variety of sterols. In addition to cholesterol, other sterols that possess the 3-beta OH at C-3, including PREG, oxysterols (such as 24(S)-hydroxycholesterol and 27-hydroxycholesterol, etc.), and various plant sterols, could all be ACAT substrates. All sterols that possess the iso-octyl side chain including cholesterol, oxysterols, various plant sterols could all be activators of ACAT. PREG can only be an ACAT substrate because it lacks the iso-octyl side chain required to be an ACAT activator. The unnatural cholesterol analogs epi-cholesterol (with 3-alpha OH in steroid ring B) and ent-cholesterol (the mirror image of cholesterol) contain the iso-octyl side chain but do not have the 3-beta OH at C-3. Thus, they can only serve as activators and cannot serve as substrates. Thus, within the ACAT holoenzyme, there are site(s) that bind sterol as substrate and site(s) that bind sterol as activator; these sites are distinct from each other. These features form the basis to further pursue ACAT structure-function analysis, and can be explored to develop novel allosteric ACAT inhibitors for therapeutic purposes. This article is part of a Special Issue entitled 'Steroid/Sterol signaling'.

Indexed as

AnimalsEsterificationHumansNeurotransmitter AgentsPregnenoloneSterol O-AcyltransferaseSterolsNeurotransmitter AgentsPregnenoloneSterol O-AcyltransferaseSterolsAcyl-CoA:cholesterol acyltransferase (ACAT/SOAT)CholesterolOxysterolsPlant sterolsPregnenolone

Identifiers

PMID25218443
PMCPMC4851438
OpenAlexW2029770517

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.