Evidence map›Paper›PMID 32413975›Full record

ArticleCancers2020

Optimization and Characterization of Protein Nanoparticles for the Targeted and Smart Delivery of Cytochrome c to Non-Small Cell Lung Carcinoma.

Vanessa Barcelo-Bovea, Irivette Dominguez-Martinez, Freisa Joaquin-Ovalle, Luis A Amador, Elizabeth Castro-Rivera, Kristofer Medina-Álvarez, Anthony McGoron, Kai Griebenow, Yancy Ferrer-Acosta

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2020. 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
0.6field-weighted citation impact, top 37% 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, 16 citations in OpenAlex.

  1. Review
  2. Article
  3. Intermolecular Electrostatic Interactions in CytochromeInternational journal of molecular sciences · 2024
    Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Membrane-Interacting DNA Nanotubes Induce Cancer Cell Death.Nanomaterials (Basel, Switzerland) · 2021
    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

9 authors at 3 institutions in 2 countries.

Vanessa Barcelo-BoveaDepartment of Chemistry, University of Puerto Rico, San Juan 00925, Puerto Rico.
Irivette Dominguez-MartinezDepartment of Chemistry, University of Puerto Rico, San Juan 00925, Puerto Rico.
Freisa Joaquin-OvalleDepartment of Chemistry, University of Puerto Rico, San Juan 00925, Puerto Rico.
Luis A AmadorDepartment of Chemistry, University of Puerto Rico, San Juan 00925, Puerto Rico.
Elizabeth Castro-RiveraDepartment of Neuroscience, Universidad Central del Caribe, Bayamon 00956, Puerto Rico.
Kristofer Medina-ÁlvarezDepartment of Neuroscience, Universidad Central del Caribe, Bayamon 00956, Puerto Rico.
Anthony McGoronDepartment of Biomedical Engineering, Florida International University, FL 33174, USA.
Kai GriebenowDepartment of Chemistry, University of Puerto Rico, San Juan 00925, Puerto Rico.
Yancy Ferrer-AcostaDepartment of Neuroscience, Universidad Central del Caribe, Bayamon 00956, Puerto Rico.ORCID 0000-0001-6489-3272
University of Puerto Rico System · PRCentral University of the Caribbean · PRFlorida International University · US

Funding

TECHNOLOGIES AND RESOURCES FOR CORE LABORATORIESU54MD007587 · NIMHD · UNIVERSITY OF PUERTO RICO MED SCIENCES · PI LUCIANO, CARLOS A., WOJNA, VALERIE · 2012 to 2018
$23.2M
NIH HHS U54MD007587NIMHD NIH HHS U54 MD007587
6 · The paper itself

Abstract

The delivery of Cytochrome c (Cyt c) to the cytosol stimulates apoptosis in cells where its release from mitochondria and apoptotic induction is inhibited. We developed a drug delivery system consisting of Cyt c nanoparticles decorated with folate-poly(ethylene glycol)-poly(lactic-co-glycolic acid)-thiol (FA-PEG-PLGA-SH) to deliver Cyt c into cancer cells and tested their targeting in the Lewis Lung Carcinoma (LLC) mouse model. Cyt c-PLGA-PEG-FA nanoparticles (NPs) of 253 ± 55 and 354 ± 11 nm were obtained by Cyt c nanoprecipitation, followed by surface decoration with the co-polymer SH-PLGA-PEG-FA. The internalization of Cyt c-PLGA-PEG-FA nanoparticles (NPs) in LLC cells was confirmed by confocal microscopy. NP caspase activation was more efficient than the NP-free formulation. Caspase activity assays showed NPs retained 88-96% Cyt c activity. The NP formulations were more effective in decreasing LLC cell viability than NP-free formulation, with IC

Indexed as

cancercytochrome cdrug deliveryLewis Lung Carcinomananoprecipitationnon-small cell lung carcinoma

Identifiers

PMID32413975
PMCPMC7281605
OpenAlexW3017225495

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.