The Anti-Proliferative Activity of Coordination Compound-Based ZnO Nanoparticles as a Promising Agent Against Triple Negative Breast Cancer Cells.
carboxylate
hexamethylenetetramine
nanoparticles
redox homeostasis imbalance
triple negative breast cancer
zinc oxide coordination compounds
Journal
International journal of nanomedicine
ISSN: 1178-2013
Titre abrégé: Int J Nanomedicine
Pays: New Zealand
ID NLM: 101263847
Informations de publication
Date de publication:
2021
2021
Historique:
received:
05
02
2021
accepted:
27
05
2021
entrez:
8
7
2021
pubmed:
9
7
2021
medline:
15
7
2021
Statut:
epublish
Résumé
The present study deals with the in vitro evaluation of the potential use of coordination compound-based zinc oxide (ZnO) nanoparticles (NPs) for the treatment of triple negative breast cancer cells (TNBrCa). As BrCa is one of the most prevalent cancer types and TNBrCa treatment is difficult due to poor prognosis and a high metastasis rate, finding a more reliable treatment option should be of the utmost interest. Prepared by reacting zinc carboxylates (formate, acetate, propionate, butyrate, isobutyrate, valerate) and hexamethylenetetramine, 4 distinct coordination compounds were further subjected to two modes of conversion into ZnO NPs - ultrasonication with oleic acid or heating of pure precursors in an air atmosphere. After detailed characterization, the resulting ZnO NPs were subjected to in vitro testing of cytotoxicity toward TNBrCa and normal breast epithelial cells. Further, their biocompatibility was evaluated. The resulting ZnO NPs provide distinct morphological features, size, biocompatibility, and selective cytotoxicity toward TNBrCa cells. They internalize into two types of TNBrCa cells and imbalance their redox homeostasis, influencing their metabolism, morphology, and ultimately leading to their death via apoptosis or necrosis. The crucial properties of ZnO NPs seem to be their morphology, size, and zinc content. The ZnO NPs with the most preferential values of all three properties show great promise for a future potential use in the therapy of TNBrCa.
Identifiants
pubmed: 34234435
doi: 10.2147/IJN.S304902
pii: 304902
pmc: PMC8257049
doi:
Substances chimiques
Antineoplastic Agents
0
Zinc Oxide
SOI2LOH54Z
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
4431-4449Informations de copyright
© 2021 Stepankova et al.
Déclaration de conflit d'intérêts
The authors report no conflicts of interest in this work.
Références
Nano Lett. 2008 Aug;8(8):2180-7
pubmed: 18605701
Mol Cancer Ther. 2020 Feb;19(2):502-512
pubmed: 31784453
Part Fibre Toxicol. 2011 Sep 06;8:27
pubmed: 21896169
Acta Crystallogr B. 2004 Apr;60(Pt 2):174-8
pubmed: 15017089
Biochim Biophys Acta. 2016 Dec;1863(12):2977-2992
pubmed: 27646922
Int J Nanomedicine. 2013;8:1835-41
pubmed: 23674895
Toxicol In Vitro. 2013 Mar;27(2):752-9
pubmed: 23274769
Mol Pharm. 2008 Jul-Aug;5(4):496-504
pubmed: 18611037
Oxid Med Cell Longev. 2014;2014:360438
pubmed: 24999379
Nat Mater. 2009 Jul;8(7):543-57
pubmed: 19525947
Nanotechnology. 2021 Mar 09;:
pubmed: 33690196
Biomolecules. 2021 Mar 05;11(3):
pubmed: 33807771
J Control Release. 2000 Mar 1;65(1-2):271-84
pubmed: 10699287
Acta Crystallogr B. 2005 Aug;61(Pt 4):429-34
pubmed: 16041092
Int J Biol Macromol. 2019 Apr 1;126:1099-1111
pubmed: 30605747
Int J Nanomedicine. 2012;7:845-57
pubmed: 22393286
Int J Nanomedicine. 2018 Jun 20;13:3441-3450
pubmed: 29950828
J Control Release. 2018 Dec 10;291:184-195
pubmed: 30367922
Nanomicro Lett. 2015;7(3):219-242
pubmed: 30464967
Nucleic Acids Res. 2003 Oct 1;31(19):5732-40
pubmed: 14500837
Biomolecules. 2019 Nov 13;9(11):
pubmed: 31766246
J Hazard Mater. 2020 Apr 15;388:122054
pubmed: 31954312
Acta Crystallogr B. 2006 Oct;62(Pt 5):745-53
pubmed: 16983155
Toxicol Sci. 2012 Apr;126(2):469-77
pubmed: 22240982
ACS Appl Mater Interfaces. 2019 Jan 9;11(1):449-456
pubmed: 30525399
Biointerphases. 2007 Dec;2(4):MR17-71
pubmed: 20419892
ESMO Open. 2017 Sep 14;2(4):e000208
pubmed: 29018573
Biopolymers. 2005 Jan;77(1):53-62
pubmed: 15578645
Anticancer Agents Med Chem. 2021;21(3):316-326
pubmed: 32698752
Nanotoxicology. 2012 Nov;6(7):746-56
pubmed: 21950449
Mater Sci Eng C Mater Biol Appl. 2021 Mar;122:111887
pubmed: 33641895
Bioconjug Chem. 2016 Oct 19;27(10):2225-2238
pubmed: 27547843
Acta Crystallogr A Found Adv. 2015 Jan;71(Pt 1):3-8
pubmed: 25537383
Nanotechnology. 2009 Nov 11;20(45):455101
pubmed: 19822937
Environ Toxicol Chem. 2012 Jan;31(1):93-9
pubmed: 21994124
Toxicol Rep. 2016 Mar 19;3:430-438
pubmed: 28959565
Semin Nephrol. 2013 Nov;33(6):479-92
pubmed: 24161035
Nanomaterials (Basel). 2020 Feb 05;10(2):
pubmed: 32033506
Mol Cancer Ther. 2006 Aug;5(8):1909-17
pubmed: 16928810
Theranostics. 2013 Dec 11;4(1):81-9
pubmed: 24396516
Acta Crystallogr C Struct Chem. 2015 Jan;71(Pt 1):3-8
pubmed: 25567568
Free Radic Res. 2010 May;44(5):479-96
pubmed: 20370557
Nat Nanotechnol. 2012 Dec;7(12):779-86
pubmed: 23212421
Spectrochim Acta A Mol Biomol Spectrosc. 2002 May;58(7):1347-64
pubmed: 12083657
J Control Release. 2020 Oct 10;326:628-647
pubmed: 32653502
Nanotechnology. 2008 Jul 23;19(29):295103
pubmed: 18836572
Chem Res Toxicol. 2010 Apr 19;23(4):733-9
pubmed: 20155942
Nanomedicine (Lond). 2019 Nov;14(21):2815-2833
pubmed: 31747855
Acta Crystallogr A. 2008 Jan;64(Pt 1):112-22
pubmed: 18156677
Sci Rep. 2020 Jan 31;10(1):1617
pubmed: 32005898
Phys Chem Chem Phys. 2017 Feb 15;19(7):5396-5404
pubmed: 28164190
Proc Natl Acad Sci U S A. 2007 Feb 13;104(7):2050-5
pubmed: 17267609