Evidence map›Paper›PMID 27432595›Full record

ArticleSmall (Weinheim an der Bergstrasse, Germany)2016

Mixed Nanosized Polymeric Micelles as Promoter of Doxorubicin and miRNA-34a Co-Delivery Triggered by Dual Stimuli in Tumor Tissue.

Giuseppina Salzano, Daniel F Costa, Can Sarisozen, Ed Luther, George Mattheolabakis, Pooja P Dhargalkar, Vladimir P Torchilin

Open access · greenAbstract read
In one paragraph

Article in Small (Weinheim an der Bergstrasse, Germany), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
7.1field-weighted citation impact, top 2% 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

27 citing papers in PubMed, 90 citations in OpenAlex.

  1. Review
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  13. Recent Advances in Stimulus-Responsive Nanocarriers for Gene Therapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2021
    Review
  14. Recent Advances in miRNA Delivery Systems.Methods and protocols · 2021
    Article
  15. Review
  16. Review
  17. Review
  18. Article
  19. Nanoscale Self-Assembly for Therapeutic Delivery.Frontiers in bioengineering and biotechnology · 2020
    Review
  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

7 authors at 3 institutions in 3 countries.

Giuseppina SalzanoCenter for Pharmaceutical Biotechnology and Nanomedicine, Northeastern University, Boston, MA, 02115, USA.
Daniel F CostaCenter for Pharmaceutical Biotechnology and Nanomedicine, Northeastern University, Boston, MA, 02115, USA.
Can SarisozenCenter for Pharmaceutical Biotechnology and Nanomedicine, Northeastern University, Boston, MA, 02115, USA.
Ed LutherDepartment of Pharmaceutical Sciences, Northeastern University, Boston, MA, 02115, USA.
George MattheolabakisDepartment of Pharmaceutical Sciences, Northeastern University, Boston, MA, 02115, USA.
Pooja P DhargalkarCenter for Pharmaceutical Biotechnology and Nanomedicine, Northeastern University, Boston, MA, 02115, USA.
Vladimir P TorchilinCenter for Pharmaceutical Biotechnology and Nanomedicine, Northeastern University, Boston, MA, 02115, USA. v.torchilin@neu.edu.
Northeastern University · USCoordenação de Aperfeicoamento de Pessoal de Nível Superior · BRKing Abdulaziz University · SA

Funding

Multifunctional matrix metalloprotease-2-sensitive anti-cancer nanopreparationsR21CA179286 · NCI · NORTHEASTERN UNIVERSITY · PI TORCHILIN, VLADIMIR P · 2014 to 2015
$372k
NCI NIH HHS R21 CA179286
6 · The paper itself

Abstract

Dual stimuli-sensitive mixed polymeric micelles (MM) are developed for co-delivery of the endogenous tumor suppressor miRNA-34a and the chemotherapeutic agent doxorubicin (Dox) into cancer cells. The novelty of the system resides in two stimuli-sensitive prodrugs, a matrix metalloproteinase 2 (MMP2)-sensitive Dox conjugate and a reducing agent (glutathione, GSH)-sensitive miRNA-34a conjugate, self-assembled in a single particle decorated with a polyethylene glycol corona for longevity, and a cell-penetrating peptide (TATp) for enhanced intracellular delivery. The MMP2-sensitivity of the system results in threefold higher cytotoxicity in MMP2-overexpressing HT1080 cells compared to low MMP2-expressing MCF7 cells. Cellular internalization of Dox increases by more than 70% after inclusion of TATp to the formulation. MMP2-sensitive MM also inhibits proliferation and migration of HT1080 cells. Moreover, GSH-sensitive MM allows for an efficient downregulation of Bcl2, survivin, and notch1 (65%, 55%, and 46%, respectively) in HT1080 cells. Combination of both conjugates in dual sensitive MM reduces HT1080 cell viability to 40% and expression of Bcl2 and survivin. Finally, 50% cell death is observed in 3D models of tumor mass. The results confirm the potential of the MM to codeliver miRNA-34a and doxorubicin triggered by dual stimuli inherent of tumor tissues.

Indexed as

Drug Delivery SystemsGene Transfer TechniquesMicellesParticle SizeApoptosisCell CycleCell Line, TumorCell SurvivalDoxorubicinGene Expression Regulation, NeoplasticGlutathioneHumansMatrix Metalloproteinase 2MicroRNAsNeoplasmsPolymersDoxorubicinGlutathioneMatrix Metalloproteinase 2MicellesMicroRNAsMIRN34 microRNA, humanPolymersdoxorubicinmiRNA-34amixed micellesspheroidstimuli-sensitive, cancer therapy

Identifiers

PMID27432595
PMCPMC5157154
OpenAlexW2484237695

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.