Evidence map›Paper›PMID 40119460›Full record

ArticleJournal of nanobiotechnology2025

Recombinant high-density lipoprotein targeted delivery of celastrol to promote foam cells lipophagy against early atherosclerosis.

Yang Li, Xiaoxia Xue, Liuchunyang Yu, Jinxiu Qian, Xiaoyu Li, Meng Tian, Jue Yang, Rongjun Deng, Cheng Lu, Cheng Xiao and 1 more

Abstract read
In one paragraph

Article in Journal of nanobiotechnology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
–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

9 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Nanomaterials-Based Immunotherapy for Atherosclerosis.Small (Weinheim an der Bergstrasse, Germany) · 2026
    Review
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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

11 authors.

Yang LiSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, China.
Xiaoxia XueSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, China.
Liuchunyang YuSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, China.
Jinxiu QianSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, China.
Xiaoyu LiSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, China.
Meng TianSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, China.
Jue YangSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, China.
Rongjun DengSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, China.
Cheng LuInstitute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences, Beijing, China. lv_cheng0816@163.com.
Cheng XiaoInstitute of Clinical Medicine, China-Japan Friendship Hospital, Beijing, China. xiaocheng@zryhyy.com.cn.
Yuanyan LiuSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, China. yyliu_1980@163.com.

Funding

the National Natural Science Foundation of China No. U22A20374
6 · The paper itself

Abstract

introductionAtherosclerosis serving as the main underlying factor of cardiovascular disease (CVD) remains the primary cause of mortality and morbidity globally, while the deposition of massive cholesterol in macrophage-derived foam cells exerts pivotal roles in the occurrence and progression of atherosclerosis. Celastrol (CEL) is a bioactive ingredient owning potent capability to modulate lipid metabolism, whereas the poor bioavailability and potential toxicity limit its clinical application.

objectivesThis study aims to design a CEL-loaded recombinant high-density lipoprotein (rHDL) delivery platform for active targeting, which may effectively promote lipid degradation in foam cells and reversely transport excessive cholesterol to the liver for metabolism in time.

methodsThe rHDL loaded with CEL (CEL-rHDL) was prepared by the thin film dispersion method. Then the anti-atherosclerotic efficacy and targeted delivery to foam cells of atherosclerotic lesions were verified both in vitro and in vivo. RNA-sequence was applied to reveal the potential mechanism against early atherosclerosis, which was further validated through several molecular biology experiments.

resultsThe prepared CEL-rHDL increased the targeting efficiency to foam cells of atherosclerotic lesions, mitigated its off-target toxicity, and improved anti-atherosclerotic efficacy. Importantly, CEL-rHDL decreased lipid storage in foam cells by triggering lipophagy via the activation of Ca

conclusionA combination of hypolipidemic chemo-intervention with rHDL participated specific and reverse delivery may offer a promising strategy for biocompatible treatment of early atherosclerosis.

Indexed as

AtherosclerosisFoam CellsLipoproteins, HDLPentacyclic TriterpenesTriterpenesAnimalsCholesterolDrug Delivery SystemsHumansLipid MetabolismMaleMiceMice, Inbred C57BLRAW 264.7 CellsRecombinant ProteinscelastrolCholesterolLipoproteins, HDLPentacyclic TriterpenesRecombinant ProteinsTriterpenesAtherosclerosisCelastrolLipophagyrHDLTargeted delivery

Identifiers

PMID40119460
PMCPMC11929195

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.