The apoptotic effects of <em>Brucea javanica</em> fruit extract against HT29 cells associated with p53 upregulation and inhibition of NF-&kappa;B translocation

Bagheri, Elham and Hajiaghaalipour, Fatemeh and Nyamathulla, Shaik and Salehen, Nur'ain (2018) The apoptotic effects of <em>Brucea javanica</em> fruit extract against HT29 cells associated with p53 upregulation and inhibition of NF-&kappa;B translocation. Drug Design, Development and Therapy, 12. pp. 657-671. ISSN 1177-8881, DOI https://doi.org/10.2147/DDDT.S155115.

Full text not available from this repository.
Official URL: https://doi.org/10.2147/DDDT.S155115

Abstract

Background: Brucea javanica (L.) Merr. is a plant from the genus Brucea, which is used in local traditional medicine to treat various diseases. Recent studies revealed an impressive anticancer efficiency of B. javanica extract in different types of cancer cells. Purpose: In this study, we have investigated the cytotoxic effects of the B. javanica hexane, ethanolic extracts against colon cancer cells. HT29 colon cells were selected as an in vitro cancer model to evaluate the anticancer activity of B. javanica ethanolic extract (BJEE) and the possible mechanisms of action that induced apoptosis. Methods: 3-(4,5-dimethylthiazol-2-yl)-2, 5,-diphenyltetrazolium bromide (MTT), lactate dehydrogenase, acridine orange/propidium iodide, and annexin-V-fluorescein isothiocyanate assays were performed to determine the antiproliferative and apoptosis validation of BJEE on cancer cells. Measurement of reactive oxygen species (ROS) production, caspase activities, nucleus factor-κB activity, and gene expression experiments was done to investigate the potential mechanisms of action in the apoptotic process. Results: The results obtained from this study illustrated the significant antiproliferative effect of BJEE on colorectal cancer cells, with a concentration value that inhibits 50% of the cell growth of 25±3.1 µg/mL after 72 h of treatment. MTT assay demonstrated that the BJEE is selectively toxic to cancer cells, and BJEE induced cell apoptosis via activation of caspase-8 along with modulation of apoptosis-related proteins such as Fas, CD40, tumor necrosis factor-related apoptosis-inducing ligands, and tumor necrosis factor receptors, which confirmed the contribution of extrinsic pathway. Meanwhile, increased ROS production in treated cells subsequently activated caspase-9 production, which triggered the intrinsic pathways. In addition, overexpression of cytochrome-c, Bax, and Bad proteins along with suppression of Bcl-2 illustrated that mitochondrial-dependent pathway also contributed to BJEE-induced cell death. Consistent with the findings from this study, BJEE-induced cancer cell death proceeds via extrinsic and intrinsic mitochondrial-dependent and -independent events. Conclusion: From the evidence obtained from this study, it is concluded that the BJEE is a promising natural extract to combat colorectal cancer cells (HT29 cells) via induction of apoptosis through activation of extrinsic and intrinsic pathways.

Item Type: Article
Funders: University of Malaya: the IPPP grant (PG053–2013A), and the UMRG research grant (RP021A-14AFR)
Uncontrolled Keywords: Brucea javanica; apoptosis; cancer; HT29; mitochondrial pathway; apoptosis protein array
Subjects: Q Science > Q Science (General)
Q Science > QH Natural history
R Medicine
Divisions: Faculty of Medicine
Faculty of Science > Institute of Biological Sciences
Depositing User: Ms. Juhaida Abd Rahim
Date Deposited: 17 Sep 2019 06:54
Last Modified: 17 Sep 2019 06:54
URI: http://eprints.um.edu.my/id/eprint/22377

Actions (login required)

View Item View Item