Evidence map›Paper›PMID 30210672›Full record

ArticleAmerican journal of translational research2018

Development of genistein-PEGylated silica hybrid nanomaterials with enhanced antioxidant and antiproliferative properties on HT29 human colon cancer cells.

Héctor Pool, Rocio Campos-Vega, María Guadalupe Herrera-Hernández, Pablo García-Solis, Teresa García-Gasca, Isaac Cornelius Sánchez, Gabriel Luna-Bárcenas, Haydé Vergara-Castañeda

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

25 citing papers in PubMed, 66 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Genistein: a promising modulator of apoptosis and survival signaling in cancer.Naunyn-Schmiedeberg's archives of pharmacology · 2023
    Review
  8. Article
  9. Review
  10. Review
  11. Nanotherapeutics in autophagy: a paradigm shift in cancer treatment.Drug delivery and translational research · 2022
    Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Review
  18. Review
  19. 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

8 authors at 3 institutions in 2 countries.

Héctor PoolCentro de Investigaciones y Estudios Avanzados (CINVESTAV) del Instituto Politécnico Nacional, Unidad Querétaro Juriquilla, Querétaro 76230, México.
Rocio Campos-VegaDepartamento de Investigación y Posgrado en Alimentos, Facultad de Química, Universidad Autónoma de Querétaro Querétaro 76010. México.
María Guadalupe Herrera-HernándezUnidad de Biotecnología, Campo Experimental Bajío, Instituto Nacional de Investigaciones Forestales, Agrícolas y Pecuarias (INIFAP) Celaya, Guanajuato 38110, México.
Pablo García-SolisDepartamento de Investigación Biomédica, Facultad de Medicina, Universidad Autónoma de Querétaro Querétaro, Querétaro 76176, México.
Teresa García-GascaFacultad de Ciencias Naturales, Universidad Autónoma de Querétaro Juriquilla, Querétaro 76230, México.
Isaac Cornelius SánchezDepartment of Chemical Engineering, The University of Texas at Austin Austin, TX 78712, USA.
Gabriel Luna-BárcenasCentro de Investigaciones y Estudios Avanzados (CINVESTAV) del Instituto Politécnico Nacional, Unidad Querétaro Juriquilla, Querétaro 76230, México.
Haydé Vergara-CastañedaDepartamento de Investigación Biomédica, Facultad de Medicina, Universidad Autónoma de Querétaro Querétaro, Querétaro 76176, México.
Center for Research and Advanced Studies of the National Polytechnic Institute · MXAutonomous University of Queretaro · MXThe University of Texas at Austin · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The anticancer use of genistein (Gen) has been severely limited due to its low water solubility, low bioavailability, and instability under experimental conditions. To overcome these limitations, we propose a formulation of a hybrid nanomaterial (HNM) based upon the incorporation of Gen into PEGylated silica nanoparticles (PEG-SiNPs) (Gen-PEG-SiHNM), where their physicochemical and biological effects on HT29 cells were evaluated. Genistein-loaded PEGylated silica hybrid nanomaterials were obtained by a simple end effective aqueous dispersion method. Physicochemical properties were determined by its mean particle size, surface charge, amount of cargo, spectroscopic properties, release profiles and aqueous solubility.

Indexed as

antiproliferative effectsColorectal cancergenisteinhybrid nanomaterialsmechanisms of programmed cell deathPEGylated silica nanoparticles

Identifiers

PMID30210672
PMCPMC6129527
OpenAlexW2994727722

What OpenQuestion holds

Textmetadata
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.