Cell Cycle Arrest and Apoptosis Induction via Modulation of Mitochondrial Integrity by Bcl-2 Family Members and Caspase Dependence in Dracaena cinnabari -Treated H400 Human Oral Squamous Cell Carcinoma

Alabsi, A.M. and Lim, K.L. and Paterson, I.C. and Ali-Saeed, R. and Muharram, B.A. (2016) Cell Cycle Arrest and Apoptosis Induction via Modulation of Mitochondrial Integrity by Bcl-2 Family Members and Caspase Dependence in Dracaena cinnabari -Treated H400 Human Oral Squamous Cell Carcinoma. BioMed Research International, 2016. p. 4904016. ISSN 2314-6133, DOI https://doi.org/10.1155/2016/4904016.

Full text not available from this repository.
Official URL: http://dx.doi.org/10.1155/2016/4904016

Abstract

Dracaena cinnabari Balf.f. is a red resin endemic to Socotra Island, Yemen. Although there have been several reports on its therapeutic properties, information on its cytotoxicity and anticancer effects is very limited. This study utilized a bioassay-guided fractionation approach to determine the cytotoxic and apoptosis-inducing effects of D. cinnabari on human oral squamous cell carcinoma (OSCC). The cytotoxic effects of D. cinnabari crude extract were observed in a panel of OSCC cell lines and were most pronounced in H400. Only fractions DCc and DCd were active on H400 cells; subfractions DCc15 and DCd16 exhibited the greatest cytotoxicity against H400 cells and D. cinnabari inhibited cells proliferation in a time-dependent manner. This was achieved primarily via apoptosis where externalization of phospholipid phosphatidylserine was observed using DAPI/Annexin V fluorescence double staining mechanism studied through mitochondrial membrane potential assay cytochrome c enzyme-linked immunosorbent and caspases activities revealed depolarization of mitochondrial membrane potential (MMP) and significant activation of caspases 9 and 3/7, concomitant with S phase arrest. Apoptotic proteins array suggested that MMP was regulated by Bcl-2 proteins family as results demonstrated an upregulation of Bax, Bad, and Bid as well as downregulation of Bcl-2. Hence, D. cinnabari has the potential to be developed as an anticancer agent.

Item Type: Article
Funders: University of Malaya, Malaysia: UMRG RP002D-13HTM and RG422/12HTM
Uncontrolled Keywords: Antineoplastic agent; Caspase; Caspase 3; Caspase 7; Caspase 8; Caspase 9; Cisplatin; Cytochrome c; DNA fragment; Dracaena cinnabari extract; Phosphatidylserine; Plant extract; Protein BAD; Protein Bax; Protein bcl 2; Protein Bid; Tumor necrosis factor related apoptosis inducing ligand; Unclassified drug; Caspase; Cytochrome c; Nucleosome; Phosphatidylserine; Plant extract; Protein bcl 2
Subjects: R Medicine > RK Dentistry
Divisions: Faculty of Dentistry
Depositing User: Ms. Juhaida Abd Rahim
Date Deposited: 09 Nov 2017 02:25
Last Modified: 09 Nov 2017 02:25
URI: http://eprints.um.edu.my/id/eprint/18182

Actions (login required)

View Item View Item