Evidence map›Paper›PMID 31408964›Full record

ArticlePharmaceutics2019

Biomimetic Magnetic Nanocarriers Drive Choline Kinase Alpha Inhibitor inside Cancer Cells for Combined Chemo-Hyperthermia Therapy.

Ylenia Jabalera, Alberto Sola-Leyva, Ana Peigneux, Federica Vurro, Guillermo R Iglesias, Jesus Vilchez-Garcia, Inmaculada Pérez-Prieto, Francisco J Aguilar-Troyano, Luisa C López-Cara, María P Carrasco-Jiménez and 1 more

Abstract read
In one paragraph

Article in Pharmaceutics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
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

14 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. 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

11 authors.

Ylenia JabaleraDepartment of Microbiology, Faculty of Sciences, University of Granada, 18071 Granada, Spain.ORCID 0000-0003-1786-959X
Alberto Sola-LeyvaDepartment of Biochemistry and Molecular Biology I, Faculty of Sciences, University of Granada, 18071 Granada, Spain.
Ana PeigneuxDepartment of Microbiology, Faculty of Sciences, University of Granada, 18071 Granada, Spain.
Federica VurroDepartment of Neurosciences, Biomedicine and Movement Sciences, Anatomy and Histology Section, University of Verona, 37134 Verona, Italy.
Guillermo R IglesiasDepartment of Applied Physics, Faculty of Sciences, University of Granada, 18071 Granada, Spain.ORCID 0000-0002-5623-1516
Jesus Vilchez-GarciaDepartment of Microbiology, Faculty of Sciences, University of Granada, 18071 Granada, Spain.
Inmaculada Pérez-PrietoDepartment of Biochemistry and Molecular Biology I, Faculty of Sciences, University of Granada, 18071 Granada, Spain.
Francisco J Aguilar-TroyanoDepartment of Pharmaceutical and Organic Chemistry, Faculty of Pharmacy, Campus of Cartuja, 18071 Granada, Spain.
Luisa C López-CaraDepartment of Pharmaceutical and Organic Chemistry, Faculty of Pharmacy, Campus of Cartuja, 18071 Granada, Spain.ORCID 0000-0003-1142-6448
María P Carrasco-JiménezDepartment of Biochemistry and Molecular Biology I, Faculty of Sciences, University of Granada, 18071 Granada, Spain. mpazcj@ugr.es.
Concepcion Jimenez-LopezDepartment of Microbiology, Faculty of Sciences, University of Granada, 18071 Granada, Spain. cjl@ugr.es.

Funding

Andalusian regional government CTS-236Ministerio de Economía y Competitividad CGL2013-46612Ministerio de Economía y Competitividad CGL2016-76723Ramón y Cajal Programme RYC-2014-16901
6 · The paper itself

Abstract

Choline kinase α1 (ChoKα1) has become an excellent antitumor target. Among all the inhibitors synthetized, the new compound Ff35 shows an excellent capacity to inhibit ChoKα1 activity. However, soluble Ff35 is also capable of inhibiting choline uptake, making the inhibitor not selective for ChoKα1. In this study, we designed a new protocol with the aim of disentangling whether the Ff35 biological action is due to the inhibition of the enzyme and/or to the choline uptake. Moreover, we offer an alternative to avoid the inhibition of choline uptake caused by Ff35, since the coupling of Ff35 to novel biomimetic magnetic nanoparticles (BMNPs) allows it to enter the cell through endocytosis without interacting with the choline transporter. This opens the possibility of a clinical use of Ff35. Our results indicate that Ff35-BMNPs nanoassemblies increase the selectivity of Ff35 and have an antiproliferative effect. Also, we demonstrate the effectiveness of the tandem Ff35-BMNPs and hyperthermia.

Indexed as

biomimeticChoKα1 inhibitordrug deliveryFf35hyperthermiamagnetic nanoparticle

Identifiers

PMID31408964
PMCPMC6722936

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.