Evidence map›Paper›PMID 40089157›Full record

ArticleMolecules and cells2025

Cholesterol sulfate as a negative regulator of cellular cholesterol homeostasis.

Le Ba Nam, Sung-Jin Kim, Tan Khanh Nguyen, Chang-Yun Jeong, June-Yong Lee, Jun-Seok Lee, Jeong Taeg Seo, Seok Jun Moon

Abstract read
In one paragraph

Article in Molecules and cells, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

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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.

Le Ba NamDepartment of Oral Biology, BK21 PLUS Project, Yonsei University College of Dentistry, Seoul 03722, Korea.
Sung-Jin KimDepartment of Oral Histology and Developmental Biology, School of Dentistry and Dental Research Institute, Seoul National University, Seoul 03080, Korea.
Tan Khanh NguyenDepartment of Oral Biology, BK21 PLUS Project, Yonsei University College of Dentistry, Seoul 03722, Korea.
Chang-Yun JeongDepartment of Microbiology, BK21 PLUS Project, Yonsei University College of Medicine, Seoul 03722, Republic of Korea.
June-Yong LeeDepartment of Microbiology, BK21 PLUS Project, Yonsei University College of Medicine, Seoul 03722, Republic of Korea.
Jun-Seok LeeDepartment of Pharmacology, Korea University College of Medicine, Seoul 02841, Republic of Korea.
Jeong Taeg SeoDepartment of Oral Biology, BK21 PLUS Project, Yonsei University College of Dentistry, Seoul 03722, Korea.
Seok Jun MoonDepartment of Oral Biology, BK21 PLUS Project, Yonsei University College of Dentistry, Seoul 03722, Korea. Electronic address: sjmoon@yuhs.ac.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cholesterol sulfate (CS), one of the most abundant cholesterol derivatives, recently emerged as a key regulatory molecule in several physiological processes. Here, we demonstrate multiple mechanisms by which CS reduces intracellular cholesterol levels. CS promotes the proteasomal degradation of 3-hydroxy-3-methylglutaryl-CoA reductase reductase by enhancing insulin-induced gene-mediated ubiquitination, thereby inhibiting cholesterol synthesis. In addition, CS blocks low-density lipoprotein receptor endocytosis, reducing low-density lipoprotein cholesterol uptake. CS further suppresses the proteolytic activation of sterol regulatory element-binding protein 2, a master transcription factor governing cholesterol synthesis and uptake. Using in vitro and in vivo models, we show that CS lowers cholesterol by targeting both the cholesterol synthesis and uptake pathways, while also modulating an important feedback loop via sterol regulatory element-binding protein 2. These findings highlight the potential of CS as a modulator of cholesterol metabolism, offering new therapeutic insights into cholesterol-related disorders.

Indexed as

CholesterolCholesterol EstersHomeostasisAnimalsEndocytosisHumansHydroxymethylglutaryl CoA ReductasesMiceReceptors, LDLSterol Regulatory Element Binding Protein 2UbiquitinationCholesterolCholesterol Esterscholesteryl sulfateHydroxymethylglutaryl CoA ReductasesReceptors, LDLSterol Regulatory Element Binding Protein 23-Hydroxy-3-methylglutaryl-CoA reductaseCholesterolCholesterol homeostasisCholesterol sulfateLow-density lipoprotein receptor

Identifiers

PMID40089157
PMCPMC12182261

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.