Evidence map›Paper›PMID 24657947›Full record

ArticleJournal of controlled release : official journal of the Controlled Release Society2014

Ultrasound-assisted siRNA delivery via arginine-grafted bioreducible polymer and microbubbles targeting VEGF for ovarian cancer treatment.

Stelios Florinas, Jaesung Kim, Kihoon Nam, Margit M Janát-Amsbury, Sung Wan Kim

Open access · greenAbstract read
In one paragraph

Article in Journal of controlled release : official journal of the Controlled Release Society, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.3field-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

28 citing papers in PubMed, 53 citations in OpenAlex.

  1. Article
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  5. Article
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  9. Review
  10. Review
  11. LncRNA-ATB in cancers: what do we know so far?Molecular biology reports · 2020
    Review
  12. Theranostic small interfering RNA nanoparticles in cancer precision nanomedicine.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2020
    Review
  13. Review
  14. Review
  15. Review
  16. Article
  17. Review
  18. Recent Progress in Gene Therapy for Ovarian Cancer.International journal of molecular sciences · 2018
    Review
  19. Article
  20. Article
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 1 institution in 1 country.

Stelios FlorinasCenter for Controlled Chemical Delivery (CCCD), Department of Pharmaceutics and Pharmaceutical Chemistry, University of Utah, Salt Lake City, USA.
Jaesung KimCenter for Controlled Chemical Delivery (CCCD), Department of Pharmaceutics and Pharmaceutical Chemistry, University of Utah, Salt Lake City, USA.
Kihoon NamCenter for Controlled Chemical Delivery (CCCD), Department of Pharmaceutics and Pharmaceutical Chemistry, University of Utah, Salt Lake City, USA.
Margit M Janát-AmsburyCenter for Controlled Chemical Delivery (CCCD), Department of Pharmaceutics and Pharmaceutical Chemistry, University of Utah, Salt Lake City, USA; Department of Obstetrics and Gynecology, Division of Gynecologic Oncology, University of Utah, Salt Lake City 84132, USA.
Sung Wan KimCenter for Controlled Chemical Delivery (CCCD), Department of Pharmaceutics and Pharmaceutical Chemistry, University of Utah, Salt Lake City, USA. Electronic address: sw.kim@pharm.utah.edu.
University of Utah · US

Funding

RGD-POLYMER TARGETING PLASMID TO ANGIOGENIC ENDOTHELIUMR01CA107070 · NCI · UNIVERSITY OF UTAH · PI KIM, SUNG WAN · 2004 to 2013
$2.7M
NCI NIH HHS CA107070NCI NIH HHS R01 CA107070
6 · The paper itself

Abstract

The major drawback hampering siRNA therapies from being more widely accepted in clinical practice is its insufficient accumulation at the target site mainly due to poor cellular uptake and rapid degradation in serum. Therefore, we designed a novel polymeric siRNA carrier system, which would withstand serum-containing environments and tested its performance in vitro as well as in vivo. Delivering siRNA with a system combining an arginine-grafted bioreducible polymer (ABP), microbubbles (MBs), and ultrasound technology (US) we were able to synergize the advantages each delivery system owns individually, and created our innovative siRNA-ABP-MB (SAM) complexes. SAM complexes show significantly higher siRNA uptake and VEGF protein knockdown in vitro with serum-containing media when compared to naked siRNA, and 25k-branched-polyethylenimine (bPEI) representing the current standard in nonviral gene therapy. SAM complexes activated by US are also able to improve siRNA uptake in tumor tissue resulting in decelerating tumor growth in vivo.

Indexed as

MicrobubblesPhonophoresisAnimalsArginineBiocompatible MaterialsCell Culture TechniquesCell Line, TumorCell SurvivalDrug CarriersDrug StabilityEnzyme-Linked Immunosorbent AssayFemaleHumansMice, NudeMicroscopy, FluorescenceOvarian NeoplasmsArgininearginine-grafted bioreducible poly(disulfide amine)polymerBiocompatible MaterialsDrug CarriersPolyaminesRNA, Small InterferingVascular Endothelial Growth Factor AVEGFA protein, humanCancerMicrobubblesRNAisiRNAUltrasoundVEGF

Identifiers

PMID24657947
PMCPMC4025968
OpenAlexW1989214948

What OpenQuestion holds

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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.