Evidence map›Paper›PMID 27347914›Full record

ArticleMolecules (Basel, Switzerland)2016

Location and Effects of an Antitumoral Catechin on the Structural Properties of Phosphatidylethanolamine Membranes.

Francisco Casado, José A Teruel, Santiago Casado, Antonio Ortiz, José N Rodríguez-López, Francisco J Aranda

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 39% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. 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

6 authors at 2 institutions in 1 country.

Francisco CasadoDepartamento de Bioquímica y Biología Molecular-A, Universidad de Murcia, Campus de Espinardo, Murcia E-30100, Spain. fcasadorojo@yahoo.es.
José A TeruelDepartamento de Bioquímica y Biología Molecular-A, Universidad de Murcia, Campus de Espinardo, Murcia E-30100, Spain. teruel@um.es.
Santiago CasadoIMDEA-Nanoscience, Campus de Cantoblanco, Madrid E-28049, Spain. santiago.casado@imdea.org.
Antonio OrtizDepartamento de Bioquímica y Biología Molecular-A, Universidad de Murcia, Campus de Espinardo, Murcia E-30100, Spain. ortizbq@um.es.
José N Rodríguez-LópezDepartamento de Bioquímica y Biología Molecular-A, Universidad de Murcia, Campus de Espinardo, Murcia E-30100, Spain. neptuno@um.es.
Francisco J ArandaDepartamento de Bioquímica y Biología Molecular-A, Universidad de Murcia, Campus de Espinardo, Murcia E-30100, Spain. fjam@um.es.
Universidad de Murcia · ESIMDEA Nanoscience · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Green tea catechins exhibit high diversity of biological effects including antioncogenic properties, and there is enormous interest in their potential use in the treatment of a number of pathologies. It is recognized that the mechanism underlying the activity of catechins relay in part in processes related to the membrane, and many studies revealed that the ability of catechins to interact with lipids plays a probably necessary role in their mechanism of action. We present in this work the characterization of the interaction between an antitumoral synthetically modified catechin (3-O-(3,4,5-trimethoxybenzoyl)-(-)-catechin, TMCG) and dimiristoylphosphatidyl-ethanolamine (DMPE) membranes using an array of biophysical techniques which include differential scanning calorimetry, X-ray diffraction, infrared spectroscopy, atomic force microscopy, and molecular dynamics simulations. We found that TMCG incorporate into DMPE bilayers perturbing the thermotropic transition from the gel to the fluid state forming enriched domains which separated into different gel phases. TMCG does not influence the overall bilayer assembly of phosphatidylethanolamine systems but it manages to influence the interfacial region of the membrane and slightly decrease the interlamellar repeat distance of the bilayer. TMCG seems to be located in the interior of the phosphatidylethanolamine bilayer with the methoxy groups being in the deepest position and some portion of the molecule interacting with the water interface. We believe that the reported interactions are significant not only from the point of view of the known antitumoral effect of TMCG, but also might contribute to understanding the basic molecular mechanism of the biological effects of the catechins found at the membrane level.

Indexed as

Antineoplastic Agents, PhytogenicCalorimetry, Differential ScanningCatechinLipid BilayersMicroscopy, Atomic ForceMolecular ConformationMolecular Dynamics SimulationPhosphatidylethanolaminesSpectroscopy, Fourier Transform InfraredX-Ray DiffractionAntineoplastic Agents, PhytogenicCatechinLipid BilayersphosphatidylethanolaminePhosphatidylethanolaminesAFMcatechinsDSCFT-IRmolecular dynamicsphosphatidylethanolamineTMCGX-ray diffraction

Identifiers

PMID27347914
PMCPMC6274109
OpenAlexW2474754851

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.