Publication: Plagioneurin B, a potent isolated compound induces apoptotic signalling pathways and cell cycle arrest in ovarian cancer cells
dc.contributor.author | Nordin, N | en_US |
dc.contributor.author | Majid, NA | en_US |
dc.contributor.author | Othman, R | en_US |
dc.contributor.author | Omer, FAA | en_US |
dc.contributor.author | Nasharuddin, MNA | en_US |
dc.contributor.author | Hashim, NM | en_US |
dc.date.accessioned | 2024-05-29T03:25:12Z | |
dc.date.available | 2024-05-29T03:25:12Z | |
dc.date.issued | 2018 | |
dc.description.abstract | Plagioneurin B belongs to acetogenin group has well-established class of compounds. Acetogenin group has attracted worldwide attention in the past few years due their biological abilities as inhibitors for several types of tumour cells. Plagioneurin B was isolated via conventional chromatography and tested for thorough mechanistic apoptosis activity on human ovarian cancer cells (CAOV-3). Its structure was also docked at several possible targets using Autodock tools software. Our findings showed that plagioneurin B successfully inhibits the growth of CAOV-3 cells at IC50 of 0.62 A mu M. The existence of apoptotic bodies, cell membrane blebbing and chromatin condensation indicated the hallmark of apoptosis. Increase of Annexin V-FITC bound to phosphatidylserine confirmed the apoptosis induction in the cells. The apoptosis event was triggered through the extrinsic and intrinsic pathways via activation of caspases 8 and 9, respectively. Stimulation of caspase 3 and the presence of DNA ladder suggested downstream apoptotic signalling were initiated. Further confirmation of apoptosis was conducted at the molecular levels where up-regulation in Bax, as well as down-regulation of Bcl-2, Hsp-70 and survivin were observed. Plagioneurin B was also seen to arrest CAOV-3 cells cycle at the G2/M phase. Docking simulation of plagioneurin B with CD95 demonstrated that the high binding affinity and hydrogen bonds formation may explain the capability of plagioneurin B to trigger apoptosis. This study is therefore importance in finding the effective compound that may offer an alternative drug for ovarian cancer treatment. | |
dc.identifier.doi | 10.1007/s10495-018-1447-x | |
dc.identifier.epage | 169 | |
dc.identifier.isbn | 1573-675X | |
dc.identifier.issn | 1360-8185 | |
dc.identifier.issue | 2 | |
dc.identifier.scopus | WOS:000425541800005 | |
dc.identifier.spage | 152 | |
dc.identifier.uri | https://oarep.usim.edu.my/handle/123456789/11904 | |
dc.identifier.volume | 23 | |
dc.language | English | |
dc.language.iso | en_US | |
dc.publisher | Springer | en_US |
dc.relation.ispartof | Apoptosis | |
dc.source | Web Of Science (ISI) | |
dc.subject | Plagioneurin B | en_US |
dc.subject | Acetogenin | en_US |
dc.subject | Ovarian cancer | en_US |
dc.subject | CAOV-3 cells | en_US |
dc.subject | Apoptosis | en_US |
dc.subject | Pathways | en_US |
dc.title | Plagioneurin B, a potent isolated compound induces apoptotic signalling pathways and cell cycle arrest in ovarian cancer cells | |
dc.type | Article | en_US |
dspace.entity.type | Publication |