Evidence map›Paper›PMID 32237116›Full record

ReviewPharmacology research & perspectives2020

Lipid-based gene delivery to macrophage mitochondria for atherosclerosis therapy.

Felix H Zakirov, Dongwei Zhang, Andrey V Grechko, Wei-Kai Wu, Anastasia V Poznyak, Alexander N Orekhov

Open access · goldAbstract readReview
In one paragraph

Review in Pharmacology research & perspectives, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 23% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. How Advanced Is Nanomedicine for Atherosclerosis?International journal of nanomedicine · 2025
    Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Review
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  10. 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

6 authors at 6 institutions in 3 countries.

Felix H ZakirovI. M. Sechenov First Moscow State Medical University (Sechenov University), Moscow, Russian Federation.
Dongwei ZhangDiabetes Research Center, Traditional Chinese Medicine School, Beijing University of Chinese Medicine, Beijing, China.
Andrey V GrechkoFederal Research and Clinical Center of Intensive Care Medicine and Rehabilitology, Moscow, Russian Federation.
Wei-Kai WuDepartment of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.
Anastasia V PoznyakInstitute for Atherosclerosis Research, Skolkovo Innovative Center, Moscow, Russia.
Alexander N OrekhovInstitute of Human Morphology, Moscow, Russia.ORCID 0000-0002-6495-1628
Beijing University of Chinese Medicine · CNInstitute for Atherosclerosis Research · RUNational Taiwan University Hospital · TWResearch Institute of General Pathology and Pathophysiology, the Russian Academy of Medical Sciences · RUSechenov University · RUV.A. Negovsky Scientific Research Institute of General Reanimatology · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Atherosclerosis with associated cardiovascular diseases remains one of the main causes of disability and death worldwide, requiring development of new solutions for prevention and treatment. Macrophages are the key effectors of a series of events involved in atherogenesis, such as inflammation, plaque formation, and changes in lipid metabolism. Some of these events were shown to be associated with mitochondrial dysfunction and excessive mitochondrial DNA (mtDNA) damage. Moreover, macrophages represent a promising target for novel therapeutic approaches that are based on the expression of various receptors and nanoparticle uptake. Lipid-based gene delivery to mitochondria is considered to be an interesting strategy for mtDNA damage correction. To date, several nanocarriers and their modifications have been developed that demonstrate high transfection efficiency and low cytotoxicity. This review discusses the possibilities of lipid-based gene delivery to macrophage mitochondria for atherosclerosis therapy.

Indexed as

Gene Transfer TechniquesAnimalsCardiovascular DiseasesDNA DamageDNA, MitochondrialHumansLipidsMacrophagesMitochondriaNanotechnologyDNA, MitochondrialLipidsatherosclerosisgene deliveryliposomesmacrophagesmitochondrial dysfunctionmtDNA damage

Identifiers

PMID32237116
PMCPMC7111069
OpenAlexW3014458416

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.