Evidence map›Paper›PMID 30323596›Full record

ArticleInternational journal of nanomedicine2018

In vitro evaluation of the antitumor effect of bismuth lipophilic nanoparticles (BisBAL NPs) on breast cancer cells.

Rene Hernandez-Delgadillo, Claudia María García-Cuéllar, Yesennia Sánchez-Pérez, Nayely Pineda-Aguilar, Marco Antonio Martínez-Martínez, Eyra Elvyra Rangel-Padilla, Sergio Eduardo Nakagoshi-Cepeda, Juan Manuel Solís-Soto, Rosa Isela Sánchez-Nájera, María Argelia Akemi Nakagoshi-Cepeda and 2 more

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

12 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. Article
  3. Biosynthesized BiFeScientific reports · 2024
    Article
  4. Review
  5. Bismuth Oxide (BiToxics · 2023
    Article
  6. Article
  7. Review
  8. Nanoparticles in Clinical Translation for Cancer Therapy.International journal of molecular sciences · 2022
    Review
  9. Review
  10. Review
  11. Article
  12. 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

12 authors at 4 institutions in 2 countries.

Rene Hernandez-DelgadilloUniversidad Autónoma de Nuevo León, UANL, Facultad de Odontología, Laboratorio de Biología Molecular, Monterrey, Nuevo León, México, claudio.cabralrm@uanl.edu.mx.
Claudia María García-CuéllarSubdirección de Investigación Básica, Instituto Nacional de Cancerología, CDMX, México.
Yesennia Sánchez-PérezSubdirección de Investigación Básica, Instituto Nacional de Cancerología, CDMX, México.
Nayely Pineda-AguilarCentro de Investigación en Materiales Avanzados, S.C. (CIMAV), Unidad Monterrey, Nuevo León, México.
Marco Antonio Martínez-MartínezUniversidad Autónoma de Nuevo León, UANL, Facultad de Odontología, Laboratorio de Biología Molecular, Monterrey, Nuevo León, México, claudio.cabralrm@uanl.edu.mx.
Eyra Elvyra Rangel-PadillaUniversidad Autónoma de Nuevo León, UANL, Facultad de Odontología, Laboratorio de Biología Molecular, Monterrey, Nuevo León, México, claudio.cabralrm@uanl.edu.mx.
Sergio Eduardo Nakagoshi-CepedaUniversidad Autónoma de Nuevo León, UANL, Facultad de Odontología, Laboratorio de Biología Molecular, Monterrey, Nuevo León, México, claudio.cabralrm@uanl.edu.mx.
Juan Manuel Solís-SotoUniversidad Autónoma de Nuevo León, UANL, Facultad de Odontología, Laboratorio de Biología Molecular, Monterrey, Nuevo León, México, claudio.cabralrm@uanl.edu.mx.
Rosa Isela Sánchez-NájeraUniversidad Autónoma de Nuevo León, UANL, Facultad de Odontología, Laboratorio de Biología Molecular, Monterrey, Nuevo León, México, claudio.cabralrm@uanl.edu.mx.
María Argelia Akemi Nakagoshi-CepedaUniversidad Autónoma de Nuevo León, UANL, Facultad de Odontología, Laboratorio de Biología Molecular, Monterrey, Nuevo León, México, claudio.cabralrm@uanl.edu.mx.
Shankararaman ChellamTexas A&M University, College Station, TX, USA.
Claudio Cabral-RomeroUniversidad Autónoma de Nuevo León, UANL, Facultad de Odontología, Laboratorio de Biología Molecular, Monterrey, Nuevo León, México, claudio.cabralrm@uanl.edu.mx.
Universidad Autónoma de Nuevo León · MXInstituto Nacional de Cancerología · MXCentro de Investigación en Materiales Avanzados · MXTexas A&M University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimThe objective of this study was to evaluate the antitumor activity of lipophilic bismuth nanoparticles (BisBAL NPs) on breast cancer cells. MATERIALS AND

methodsThe effect of varying concentrations of BisBAL NPs was evaluated on human MCF-7 breast cancer cells and on MCF-10A fibrocystic mammary epitheliocytes as noncancer control cells. Cell viability was evaluated with the MTT assay, plasma membrane integrity was analyzed with the calcein AM assay, genotoxicity with the comet assay, and apoptosis with the Annexin V/7-AAD assay.

resultsBisBAL NPs were spherical in shape (average diameter, 28 nm) and agglomerated into dense electronic clusters. BisBAL NP induced a dose-dependent growth inhibition. Most importantly, growth inhibition was higher for MCF-7 cells than for MCF-10A cells. At 1 µM BisBAL NP, MCF-7 growth inhibition was 51%, while it was 11% for MCF-10A; at 25 µM BisBAL NP, the growth inhibition was 81% for MCF-7 and 24% for MCF-10A. With respect to mechanisms of action, a 24-hour exposure of 10 and 100 µM BisBAL NP caused loss of cell membrane integrity and fragmentation of tumor cell DNA. BisBAL NPs at 10 µM were genotoxic to and caused apoptosis of breast cancer cells.

conclusionBisBAL NP-induced growth inhibition is dose dependent, and breast cancer cells are more vulnerable than noncancer breast cells. The mechanism of action of BisBAL NPs may include loss of plasma membrane integrity and a genotoxic effect on the genomic DNA of breast cancer cells.

Indexed as

Antineoplastic AgentsApoptosisBismuthBreast NeoplasmsCell Membrane PermeabilityCell SurvivalComet AssayDimercaprolDNA DamageFemaleHumansMCF-7 CellsNanoparticlesOrganometallic CompoundsAntineoplastic AgentsBismuthbismuth dimercaptopropanolDimercaprolOrganometallic Compoundsantitumor activitybismuth nanoparticlesbreast cancerchemotherapycytotoxicity

Identifiers

PMID30323596
PMCPMC6179729
OpenAlexW2895448378

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.