Citation
Abstract
Background: This study reports on the cytotoxic properties of nordamnacanthal and damnacanthal, isolated from roots of Morinda elliptica on T-lymphoblastic leukaemia (CEM-SS) cell lines. Methods: MTT assay, DNA fragmentation, ELISA and cell cycle analysis were carried out. Results: Nordamnacanthal and damnacanthal at IC50 values of 1.7 μg/mL and10 μg/mL, respectively. At the molecular level, these compounds caused internucleosomal DNA cleavage producing multiple 180–200 bp fragments that are visible as a “ladder” on the agarose gel. This was due to the activation of the Mg2+/Ca2+-dependent endonuclease. The induction of apoptosis by nordamnacanthal was different from the one induced by damnacanthal, in a way that it occurs independently of ongoing transcription process. Nevertheless, in both cases, the process of dephosphorylation of protein phosphates 1 and 2A, the ongoing protein synthesis and the elevations of the cytosolic Ca2+ concentration were not needed for apoptosis to take place. Nordamnacanthal was found to have a cytotoxic effect by inducing apoptosis, while damnacanthal caused arrest at the G0/G1 phase of the cell cycle. Conclusion: Damnacanthal and nordamnacanthal have anticancer properties, and could act as potential treatment for T-lymphoblastic leukemia.
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Official URL or Download Paper: https://www.mdpi.com/1420-3049/26/6/1554
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Additional Metadata
Item Type: | Article |
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Divisions: | Faculty of Biotechnology and Biomolecular Sciences Faculty of Medicine and Health Science Institute of Bioscience |
DOI Number: | https://doi.org/10.3390/molecules26061554 |
Publisher: | Multidisciplinary Digital Publishing Institute |
Keywords: | Damnacanthal; Nordamnacanthal; Anticancer; CEM-SS; Apoptosis; Mg2+/Ca2+-dependent endonuclease; G0/G1 arrest; Cytotoxic |
Depositing User: | Ms. Nuraida Ibrahim |
Date Deposited: | 27 Mar 2023 03:35 |
Last Modified: | 27 Mar 2023 03:35 |
Altmetrics: | http://www.altmetric.com/details.php?domain=psasir.upm.edu.my&doi=10.3390/molecules26061554 |
URI: | http://psasir.upm.edu.my/id/eprint/95902 |
Statistic Details: | View Download Statistic |
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