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Multi-targeted potential of Pittosporum senacia Putt.: HPLC-ESI-MSn analysis, in silico docking, DNA protection, antimicrobial, enzyme inhibition, anti-cancer and apoptotic activity

dc.contributor.authorMahomoodally M. F.
dc.contributor.authorPicot-Allain C.
dc.contributor.authorHosenally M.
dc.contributor.authorUgurlu A.
dc.contributor.authorMollica A.
dc.contributor.authorStefanucci A.
dc.contributor.authorLlorent-Martinez E. J.
dc.contributor.authorBaloglu M. C.
dc.contributor.authorZengin G.
dc.date.accessioned2026-01-05T22:58:58Z
dc.date.issued2019-12-01
dc.description.abstractPittosporum senacia (PS) Putt. (Pittosporaceae), indigenous to the Mascarene Islands, is a common ingredient in traditional medicines. However, there is currently a dearth of studies to validate some of these traditional claims. Given the broad traditional uses of PS against several diseases, we aimed to provide a comprehensive insight into the biological and chemical profile of P. senacia. The antioxidant, enzyme inhibitory activity, anticancer, and phytochemical composition of the methanolic extract of P. senacia leaf extracts were studied. The possible interaction and binding mode of the most abundant phytochemicals were studied via in silico docking experiments on tyrosinase and α-glucosidase. The mechanism behind the cytotoxic property of P. senacia extract for MDA-MB-231 was also examined using different methods including 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) cell viability test checking apoptosis-associated genes, and wound healing assays. Twenty-six compounds were identified, of which caffeoylquinic acid derivatives, ferulic acid derivative, cinnamoylquinic acid derivative and two other polyphenols (oleuropeine and isoramnetin glucoside) being abundant, have been tested using in silico studies, against α-glucosidase and tyrosinase. The extract (IC50 = 118.8 μg/ml) exhibited time and dose dependent anti-proliferative effect on human breast cancer cell line, MDA-MB-231. According to the expression profile of apoptosis inhibitors and apoptosis promoters genes, expression of Bax and Bak genes were significantly increased compared to Bcl-2 and Birc5 genes. Based on wound healing analysis, cell migration was inhibited after the application of the plant extract. The present findings suggested that PS might be a good candidate as sources of bioactive compounds for designing functional applications.
dc.description.urihttps://doi.org/10.1016/j.compbiolchem.2019.107114
dc.description.urihttps://pubmed.ncbi.nlm.nih.gov/31493741
dc.description.urihttps://dx.doi.org/10.1016/j.compbiolchem.2019.107114
dc.description.urihttps://hdl.handle.net/11564/717651
dc.description.urihttps://www.sciencedirect.com/science/article/pii/S1476927119306590?via=ihub
dc.description.urihttps://hdl.handle.net/20.500.12395/38020
dc.identifier.doi10.1016/j.compbiolchem.2019.107114
dc.identifier.issn1476-9271
dc.identifier.openairedoi_dedup___::4ad050a6da9ff3066ba3899866867226
dc.identifier.orcid0000-0003-2131-2823
dc.identifier.orcid0000-0002-7242-4860
dc.identifier.orcid0000-0001-7525-2913
dc.identifier.orcid0000-0002-0180-5172
dc.identifier.orcid0000-0001-6548-7823
dc.identifier.pubmed31493741
dc.identifier.scopus2-s2.0-85071661076
dc.identifier.startpage107114
dc.identifier.urihttps://hdl.handle.net/20.500.12597/43491
dc.identifier.volume83
dc.identifier.wos000501651500023
dc.language.isoeng
dc.publisherElsevier BV
dc.relation.ispartofComputational Biology and Chemistry
dc.rightsOPEN
dc.subjectSpectrometry, Mass, Electrospray Ionization
dc.subjectPittosporaceae
dc.subjectCell Survival
dc.subjectApoptosis
dc.subjectMicrobial Sensitivity Tests
dc.subjectGram-Positive Bacteria
dc.subjectGram-Negative Bacteria
dc.subjectTumor Cells, Cultured
dc.subjectHumans
dc.subjectEnzyme Inhibitors
dc.subjectRosales
dc.subjectAntimicrobial
dc.subjectApoptosis
dc.subjectDiabetes
dc.subjectMauritius
dc.subjectPittosporaceae
dc.subjectAnti-Bacterial Agents
dc.subjectAntineoplastic Agents, Phytogenic
dc.subjectApoptosis
dc.subjectCell Proliferation
dc.subjectCell Survival
dc.subjectChromatography, High Pressure Liquid
dc.subjectDNA
dc.subjectDrug Screening Assays, Antitumor
dc.subjectEnzyme Inhibitors
dc.subjectGram-Negative Bacteria
dc.subjectGram-Positive Bacteria
dc.subjectHumans
dc.subjectMicrobial Sensitivity Tests
dc.subjectMonophenol Monooxygenase
dc.subjectPlant Extracts
dc.subjectPlasmids
dc.subjectRosales
dc.subjectSpectrometry, Mass, Electrospray Ionization
dc.subjectTumor Cells, Cultured
dc.subjectalpha-Glucosidases
dc.subjectMolecular Docking Simulation
dc.subjectChromatography, High Pressure Liquid
dc.subjectCell Proliferation
dc.subjectMonophenol Monooxygenase
dc.subjectPlant Extracts
dc.subjectDiabetes
dc.subjectDNA
dc.subjectAntineoplastic Agents, Phytogenic
dc.subjectAnti-Bacterial Agents
dc.subjectMolecular Docking Simulation
dc.subjectMauritius
dc.subjectAntimicrobial
dc.subjectDrug Screening Assays, Antitumor
dc.subjectPlasmids
dc.subject.sdg3. Good health
dc.titleMulti-targeted potential of Pittosporum senacia Putt.: HPLC-ESI-MSn analysis, in silico docking, DNA protection, antimicrobial, enzyme inhibition, anti-cancer and apoptotic activity
dc.typeArticle
dspace.entity.typePublication
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Given the broad traditional uses of PS against several diseases, we aimed to provide a comprehensive insight into the biological and chemical profile of P. senacia. The antioxidant, enzyme inhibitory activity, anticancer, and phytochemical composition of the methanolic extract of P. senacia leaf extracts were studied. The possible interaction and binding mode of the most abundant phytochemicals were studied via in silico docking experiments on tyrosinase and α-glucosidase. The mechanism behind the cytotoxic property of P. senacia extract for MDA-MB-231 was also examined using different methods including 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) cell viability test checking apoptosis-associated genes, and wound healing assays. Twenty-six compounds were identified, of which caffeoylquinic acid derivatives, ferulic acid derivative, cinnamoylquinic acid derivative and two other polyphenols (oleuropeine and isoramnetin glucoside) being abundant, have been tested using in silico studies, against α-glucosidase and tyrosinase. The extract (IC50 = 118.8 μg/ml) exhibited time and dose dependent anti-proliferative effect on human breast cancer cell line, MDA-MB-231. According to the expression profile of apoptosis inhibitors and apoptosis promoters genes, expression of Bax and Bak genes were significantly increased compared to Bcl-2 and Birc5 genes. Based on wound healing analysis, cell migration was inhibited after the application of the plant extract. 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