Molecular Investigation of the Antitumor Effects of Monoamine Oxidase Inhibitors in Breast Cancer Cells.


Journal

BioMed research international
ISSN: 2314-6141
Titre abrégé: Biomed Res Int
Pays: United States
ID NLM: 101600173

Informations de publication

Date de publication:
2023
Historique:
received: 21 09 2022
revised: 05 09 2023
accepted: 19 09 2023
medline: 23 10 2023
pubmed: 16 10 2023
entrez: 16 10 2023
Statut: epublish

Résumé

The catalytic activity of monoamine oxidase A (MAO-A) has been linked to tumorigenesis due to the production of reactive oxygen species (ROS) and the resulting oxidative stress. MAO-A inhibition revealed a beneficial role in prostate and lung cancer treatment. This study is aimed at evaluating the effect of different monoamine oxidase A inhibitors (MAO-AIs) on the proliferation and progression of breast cancer cell lines. The cell viability assay was used to evaluate the antiproliferative and combined effects of MAO-AIs. Cell migration was evaluated using wound healing, invasion, and colony formation assays. The underlying mechanism of cell death was studied using flow cytometry. The real-time polymerase chain reaction was used to determine the relative gene expression. Finally, MAO-A activity in breast cancer cells was evaluated using an MAO-A activity assay. According to the results, the examined MAO-AIs significantly inhibited the proliferation of breast cancer cells in a dose-dependent manner. In breast cancer cells, the combination of anticancer drugs (doxorubicin or raloxifene) with MAO-AIs resulted in a synergistic effect. MAO-AIs significantly reduced wound closure and invasion ability in breast cancer cells. Also, MAO-AIs reduced the colony count and size of breast cancer cells. MAO-AIs resulted in significant proapoptotic activity in breast cancer cells. Finally, the MAO-AIs suppressed

Identifiants

pubmed: 37841082
doi: 10.1155/2023/2592691
pmc: PMC10569896
doi:

Substances chimiques

Monoamine Oxidase Inhibitors 0
Monoamine Oxidase EC 1.4.3.4
Reactive Oxygen Species 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2592691

Informations de copyright

Copyright © 2023 Aseel Alkhawaldeh and Sanaa Bardaweel.

Déclaration de conflit d'intérêts

The authors declare no conflict of interest.

Références

Cancer Med. 2020 Nov;9(21):8004-8019
pubmed: 32931665
Oncogene. 2018 Sep;37(38):5175-5190
pubmed: 29844571
Prostate. 2019 May;79(6):667-677
pubmed: 30693539
Anticancer Agents Med Chem. 2022;22(18):3114-3124
pubmed: 35473535
Cell Signal. 2014 Dec;26(12):2621-32
pubmed: 25152370
J Clin Invest. 2014 Jul;124(7):2891-908
pubmed: 24865426
Cell Mol Biol Lett. 2019 Nov 12;24:59
pubmed: 31754354
Cold Spring Harb Perspect Med. 2016 Mar 01;6(3):a026104
pubmed: 26931810
Hypertension. 2013 Jul;62(1):140-6
pubmed: 23670301
Curr Med Chem. 2009;16(25):3267-85
pubmed: 19548866
J Hepatol. 2014 Jun;60(6):1225-34
pubmed: 24607627
Sci Rep. 2019 Jul 29;9(1):10989
pubmed: 31358840
Prog Neuropsychopharmacol Biol Psychiatry. 2014 Jan 3;48:102-11
pubmed: 24104186
Eurasian J Med. 2018 Oct;50(3):193-201
pubmed: 30515042
J Neural Transm (Vienna). 2018 Nov;125(11):1553-1566
pubmed: 30259128
Int J Biol Sci. 2020 Aug 1;16(14):2692-2703
pubmed: 32792865
J Pathol. 2017 Oct;243(2):220-229
pubmed: 28722111
Int J Mol Sci. 2017 Dec 20;18(12):
pubmed: 29261141
Tumour Biol. 2014 Nov;35(11):10635-44
pubmed: 25238879
Expert Opin Ther Targets. 2017 Oct;21(10):959-966
pubmed: 28831824
CA Cancer J Clin. 2021 May;71(3):209-249
pubmed: 33538338
Pharmaceutics. 2011 Mar 11;3(1):107-24
pubmed: 24310428
Acta Pharm. 2020 Jun 1;70(2):179-190
pubmed: 31955147
Prog Neuropsychopharmacol Biol Psychiatry. 2013 Jul 1;44:118-24
pubmed: 23410524
Molecules. 2020 Dec 25;26(1):
pubmed: 33375766
Antimicrob Agents Chemother. 2012 Mar;56(3):1508-15
pubmed: 22203607
Molecules. 2022 Apr 30;27(9):
pubmed: 35566238
Nat Clin Pract Oncol. 2007 Mar;4(3):181-9
pubmed: 17327858
Molecules. 2021 Oct 04;26(19):
pubmed: 34641563
BMC Med Genomics. 2009 Aug 20;2:55
pubmed: 19691856
Curr Opin Pharmacol. 2017 Apr;33:64-69
pubmed: 28528298
Molecules. 2020 May 11;25(9):
pubmed: 32403270
J Mol Cell Cardiol. 2014 Aug;73:34-42
pubmed: 24412580
J Urol. 2008 Nov;180(5):2206-11
pubmed: 18804811
Cancer Res. 1996 May 1;56(9):2013-6
pubmed: 8616842
Cancer Res. 2010 Jan 15;70(2):440-6
pubmed: 20068163
CA Cancer J Clin. 2023 Jan;73(1):17-48
pubmed: 36633525
BMC Complement Altern Med. 2014 Aug 12;14:297
pubmed: 25112895
Oncol Lett. 2018 Mar;15(3):3245-3251
pubmed: 29435065
Adv Hematol. 2012;2012:524308
pubmed: 21941553
Nat Commun. 2020 Jun 1;11(1):2689
pubmed: 32483206
Oncotarget. 2016 Mar 22;7(12):13842-53
pubmed: 26871599
PLoS One. 2014 Sep 08;9(9):e104271
pubmed: 25198178
Int J Breast Cancer. 2011;2011:967419
pubmed: 22332018
Sci Rep. 2016 Feb 24;6:21986
pubmed: 26906215

Auteurs

Aseel Alkhawaldeh (A)

Department of Pharmaceutical Sciences, School of Pharmacy, University of Jordan, Queen Rania Street, Amman 11942, Jordan.

Sanaa Bardaweel (S)

Department of Pharmaceutical Sciences, School of Pharmacy, University of Jordan, Queen Rania Street, Amman 11942, Jordan.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH