Evidence map›Paper›PMID 20568694›Full record

ArticleMolecular pharmaceutics2010

Effect of cholesterol nanodomains on the targeting of lipid-based gene delivery in cultured cells.

Long Xu, Thomas J Anchordoquy

Open access · greenAbstract read
In one paragraph

Article in Molecular pharmaceutics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

20 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Article
  3. Anti-F1000Research · 2020
    Article
  4. Article
  5. Nanoparticle uptake by circulating leukocytes: A major barrier to tumor delivery.Journal of controlled release : official journal of the Controlled Release Society · 2018
    Article
  6. Article
  7. Intracellular trafficking of hybrid gene delivery vectors.Journal of controlled release : official journal of the Controlled Release Society · 2015
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Questioning the Use of PEGylation for Drug Delivery.Drug delivery and translational research · 2013
    Article
  14. The effects of lipoplex formulation variables on the protein corona and comparisons with in vitro transfection efficiency.Journal of controlled release : official journal of the Controlled Release Society · 2013
    Article
  15. Article
  16. Cholesterol domains enhance transfection.Therapeutic delivery · 2013
    Article
  17. Article
  18. Ligands located within a cholesterol domain enhance gene delivery to the target tissue.Journal of controlled release : official journal of the Controlled Release Society · 2012
    Article
  19. Article
  20. 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

2 authors at 1 institution in 1 country.

Long XuSchool of Pharmacy, University of Colorado Denver, 12700 East 19th Avenue, Aurora, Colorado 80045, USA.
Thomas J Anchordoquy
University of Colorado Denver · US

Funding

Formulation of Synthetic Vectors as Lyophilized ProductsR01EB005476 · NIBIB · UNIVERSITY OF COLORADO DENVER · PI ANCHORDOQUY, THOMAS · 2006 to 2009
$947k
NIBIB NIH HHS EB0005476-01A2NIBIB NIH HHS R01 EB005476
6 · The paper itself

Abstract

Targeted gene delivery offers immense potential for clinical applications. Liposomes decorated with targeting ligands have been extensively used for both in vitro and in vivo gene delivery. Lipoplexes with high cholesterol content that result in cholesterol domain formation within the complexes have been shown to exhibit enhanced transfection in vitro and resistance to serum-induced aggregation. In the present study, folate was employed as a targeting ligand that was conjugated with either cholesterol or a diacyl lipid (DSPE), and these conjugates were incorporated into lipoplexes formulated with DOTAP/cholesterol (wt/wt: 31/69) that are known to possess cholesterol nanodomains. Cellular uptake and transfection of these lipoplexes in the presence of 50% serum were examined when the ligand was located within or excluded from the cholesterol nanodomain. Lipoplexes with folate-cholesterol exhibited a 50-fold increase in transfection compared to those with folate-DSPE, while the cellular uptake level is only 40% of that with folate-DSPE. These results indicate that the presence of the ligand within the cholesterol domain promotes more productive transfection in cultured cells, and intracellular trafficking of the lipoplexes after entry into cells plays a crucial role in gene delivery.

Indexed as

Gene Transfer TechniquesCalorimetry, Differential ScanningCell Line, TumorCholesterolFatty Acids, MonounsaturatedFlow CytometryFolic AcidHumansLiposomesPhosphatidylethanolaminesQuaternary Ammonium CompoundsScattering, Radiation1,2-dioleoyloxy-3-(trimethylammonium)propane1,2-distearoylphosphatidylethanolamineCholesterolFatty Acids, MonounsaturatedFolic AcidLiposomesPhosphatidylethanolaminesQuaternary Ammonium Compounds

Identifiers

PMID20568694
PMCPMC3307044
OpenAlexW1980522895

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.