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Apoptosis Induced by (+)-Betulin Through NF-κB Inhibition in MDA-MB-231 Breast Cancer Cells.
- Source :
-
Anticancer research [Anticancer Res] 2020 Dec; Vol. 40 (12), pp. 6637-6647. Date of Electronic Publication: 2020 Dec 07. - Publication Year :
- 2020
-
Abstract
- Background/aim: This study aimed to uncover the effects of (+)-betulin on the NF-κB-apoptotic pathway in MDA-MB-231 cells, and determine its toxicity and protein expression in vivo.<br />Materials and Methods: Cell cytotoxicity and toxicity were determined using the SRB assay and a zebrafish model, respectively. Western blot, mitochondrial transmembrane potential (MTP), and computational modeling analysis were performed.<br />Results: (+)-betulin inhibited the growth of MDA-MB-231 cells, but did not induce toxicity in zebrafish. (+)-Betulin inhibited the activity of NF-κB p65 in silico and in vitro. In cells, (+)-betulin down-regulated NF-κB p50 and 65, IKKα and β, ICAM-1 and bcl-2 expressions. Cell co-treatment with (+)-betulin and TNFα increased the (+)-betulin cytotoxic potential. Moreover, (+)-betulin induced the loss of MTP. Furthermore, (+)-betulin, in zebrafish, down-regulated the expression of NF-κB p65, IKKα, ΙΚΚβ and procaspase-3.<br />Conclusion: The results contribute to the understanding of the mode of action on apoptosis induction by inhibiting NF-κB pathway in MDA-MB-231 cells.<br /> (Copyright © 2020 International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.)
- Subjects :
- Animals
Cell Line, Tumor
Female
Humans
Membrane Potential, Mitochondrial drug effects
Molecular Docking Simulation
NF-kappa B metabolism
Proto-Oncogene Proteins c-bcl-2 metabolism
Signal Transduction drug effects
Triterpenes chemistry
Tumor Necrosis Factor-alpha pharmacology
Zebrafish
Apoptosis drug effects
Breast Neoplasms pathology
NF-kappa B antagonists & inhibitors
Triterpenes pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1791-7530
- Volume :
- 40
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- Anticancer research
- Publication Type :
- Academic Journal
- Accession number :
- 33288558
- Full Text :
- https://doi.org/10.21873/anticanres.14688