Evidence map›Paper›PMID 36831097›Full record

ReviewBiomedicines2023

Biomedical Advances in ABCA1 Transporter: From Bench to Bedside.

Hong Y Choi, Senna Choi, Iulia Iatan, Isabelle Ruel, Jacques Genest

Open access · goldAbstract readReview
In one paragraph

Review in Biomedicines, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

12 citing papers in PubMed, 13 citations in OpenAlex.

  1. Journal of clinical medicine · 2026
    Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Role ofCurrent medicinal chemistry · 2025
    Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
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

5 authors at 2 institutions in 1 country.

Hong Y ChoiResearch Institute of the McGill University Health Centre, Montréal, QC H4A 3J1, Canada.ORCID 0000-0003-2477-1128
Senna ChoiResearch Institute of the McGill University Health Centre, Montréal, QC H4A 3J1, Canada.
Iulia IatanCentre for Heart Lung Innovation, Department of Medicine, St. Paul's Hospital, University of British Columbia, Vancouver, BC V6Z 1Y6, Canada.
Isabelle RuelResearch Institute of the McGill University Health Centre, Montréal, QC H4A 3J1, Canada.ORCID 0000-0002-9491-8028
Jacques GenestResearch Institute of the McGill University Health Centre, Montréal, QC H4A 3J1, Canada.
McGill University Health Centre · CAUniversity of British Columbia · CA

Funding

The Canadian Institutes of Health Research PJT-165924
6 · The paper itself

Abstract

ATP-binding cassette transporter A1 (ABCA1) has been identified as the molecular defect in Tangier disease. It is biochemically characterized by absence of high-density lipoprotein cholesterol (HDL-C) in the circulation, resulting in the accumulation of cholesterol in lymphoid tissues. Accumulation of cholesterol in arteries is an underlying cause of atherosclerosis, and HDL-C levels are inversely associated with the presence of atherosclerotic cardiovascular disease (ASCVD). ABCA1 increases HDL-C levels by driving the generation of new HDL particles in cells, and cellular cholesterol is removed in the process of HDL generation. Therefore, pharmacological strategies that promote the HDL biogenic process by increasing ABCA1 expression and activity have been intensively studied to reduce ASCVD. Many ABCA1-upregulating agents have been developed, and some have shown promising effects in pre-clinical studies, but no clinical trials have met success yet. ABCA1 has long been an attractive drug target, but the failed clinical trials have indicated the difficulty of therapeutic upregulation of ABCA1, as well as driving us to: improve our understanding of the ABCA1 regulatory system; to develop more specific and sophisticated strategies to upregulate ABCA1 expression; and to search for novel druggable targets in the ABCA1-dependent HDL biogenic process. In this review, we discuss the beginning, recent advances, challenges and future directions in ABCA1 research aimed at developing ABCA1-directed therapies for ASCVD.

Indexed as

ABCA1atherosclerosischolesteroldesmocollin 1docetaxelhigh-density lipoprotein

Identifiers

PMID36831097
PMCPMC9953649
OpenAlexW4320918042

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.