Evidence map›Paper›PMID 23978682›Full record

ArticleJournal of controlled release : official journal of the Controlled Release Society2013

Incorporation of histone derived recombinant protein for enhanced disassembly of core-membrane structured liposomal nanoparticles for efficient siRNA delivery.

Yuhua Wang, Lu Zhang, Shutao Guo, Arash Hatefi, Leaf Huang

Abstract read
In one paragraph

Article in Journal of controlled release : official journal of the Controlled Release Society, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.2field-weighted citation impact, top 12% 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, 32 citations in OpenAlex.

  1. Review
  2. Stimuli-responsive liposomes for drug delivery.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2017
    Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Controlled release from recombinant polymers.Journal of controlled release : official journal of the Controlled Release Society · 2014
    Review
  8. Article
  9. Composite nanoparticles for gene delivery.Advances in genetics · 2014
    Review
  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

5 authors at 2 institutions in 1 country.

Yuhua WangDivision of Molecular Pharmaceutics and Center for Nanotechnology in Drug Delivery, Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, USA. Electronic address: alwang@email.unc.edu.
Lu ZhangDivision of Molecular Pharmaceutics and Center for Nanotechnology in Drug Delivery, Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, USA.
Shutao GuoDivision of Molecular Pharmaceutics and Center for Nanotechnology in Drug Delivery, Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, USA.
Arash HatefiDepartment of Pharmaceutics, Ernest Mario School of Pharmacy, University of Rutgers, Piscataway, USA.
Leaf HuangDivision of Molecular Pharmaceutics and Center for Nanotechnology in Drug Delivery, Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, USA.
University of North Carolina at Chapel Hill · USRutgers, The State University of New Jersey · US

Funding

Translational Nanosystems for Improved Lung Cancer Treatment with Small MoleculesU54CA151652 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI HAROON, ZISHAN A, TEPPER, JOEL E · 2010 to 2014
$12.1M
Nanoscale Metal-organic Frameworks for Imaging and Therapy of Pancreatic CancerU01CA151455 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LIN, WENBIN, YEH, JEN JEN · 2010 to 2014
$2.1M
LPD Nanoparticles in Anti-Cancer TherapyR01CA129835 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI HUANG, LEAF · 2008 to 2012
$1.5M
Interaction of cationic lipids with dendritic cellsR01CA129421 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI HUANG, LEAF · 2008 to 2012
$1.5M
Novel nanoparticles for siRNA deliveryR01CA149363 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI HUANG, LEAF · 2010 to 2014
$1.3M
NCI NIH HHS CA129421NCI NIH HHS CA129835NCI NIH HHS CA149363NCI NIH HHS CA151455NCI NIH HHS CA151652NCI NIH HHS R01 CA129421NCI NIH HHS R01 CA129835NCI NIH HHS R01 CA149363NCI NIH HHS U01 CA151455NCI NIH HHS U54 CA151652
6 · The paper itself

Abstract

A novel recombinant protein tetra-H2A (TH) derived from histone H2A has been developed to replace protamine as a conditionally reversible, nucleic acid condensing agent. The novel protein will address the insufficient release of nucleic acid therapeutics, which is captured by protamine for siRNA delivery. TH is composed of 4 tandem repeats of the histone H2A N-terminal sequence, intervened by the cathepsin D cleavage site. The repeating H2A sequence enhances the binding affinity to anionic nucleic acids, forming more stable condensates, as demonstrated by the binding affinity assay. The TH/siRNA condensates are formulated into a core-membrane structured liposomal nanoparticle (NP). The endosomes of cancer cells are rich in cathepsin D, allowing on-site degradation of TH and facilitating the intracellular release of siRNA. The NPs assembled with TH produced a higher silencing efficiency of target genes in vitro and in vivo than the NPs assembled with protamine as the nucleic acid condensing agent. The exploitation of TH in the NP formulation exhibited a biocompatibility profile similar to that of protamine, with minimal immunostimulating and systemic toxicity observed after repeated administration.

Indexed as

RNA InterferenceAmino Acid SequenceAnimalsCell Line, TumorCloning, MolecularFemaleHistonesHumansLiposomesMiceMice, NudeMolecular Sequence DataNanoparticlesPolyethylene GlycolsRecombinant ProteinsRNA, Small InterferingHistonesLiposomesPolyethylene GlycolsRecombinant ProteinsRNA, Small Interfering1,2-dioctadecanoyl-sn-glycero-3-phosphoethanolamine1,2-dioleoyl-3-trimethylammonium-propaneDOTAPDSPELiposomeNanoparticleRecombinant proteinRNAitetra-H2A polypeptidetetra-H2A polypeptide without cathepsin D cleavage sitetetra-H2A polypeptide without GALAtetra-H2A polypeptide without GALA or cathepsin D cleavage siteTHTH/ΔCathDTH/ΔGALATH/ΔGALA/ΔCathDTumor targeted delivery

Identifiers

PMID23978682
PMCPMC5020560
OpenAlexW2023364583

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.