Exploring the Anticancer Potential of Premna resinosa (Hochst.) Leaf Surface Extract: Discovering New Diterpenes as Heat Shock Protein 70 (Hsp70) Binding Agents.
Valentina ParisiGiuliana DonadioMaria Laura BelloneSoumia BelaabedAmmar BaderAngela BisioValeria IobbiErica GazzilloMaria Giovanna ChiniGiuseppe BifulcoImmacolata FaraoneAntonio VassalloPublished in: Plants (Basel, Switzerland) (2023)
Premna , a genus consisting of approximately 200 species, predominantly thrives in tropical and subtropical areas. Many of these species have been utilized in ethnopharmacology for diverse medicinal applications. In Saudi Arabia, Premna resinosa (Hochst.) Schauer (Lamiaceae) grows wildly, and its slightly viscid leaves are attributed to the production of leaf accession. In this study, we aimed to extract the surface accession from fresh leaves using dichloromethane to evaluate the anticancer potential. The plant exudate yielded two previously unknown labdane diterpenes, Premnaresone A and B, in addition to three already described congeners and four known flavonoids. The isolation process was accomplished using a combination of silica gel column chromatography and semi-preparative HPLC, the structures of which were identified by NMR and HRESIMS analyses and a comparison with the literature data of associated compounds. Furthermore, we employed a density functional theory (DFT)/NMR approach to suggest the relative configuration of different compounds. Consequently, we investigated the possibility of developing new chaperone inhibitors by subjecting diterpenes 1 - 5 to a Surface Plasmon Resonance-screening, based on the knowledge that oridonin, a diterpene, interacts with Heat Shock Protein 70 (Hsp70) 1A in cancer cells. Additionally, we studied the anti-proliferative activity of compounds 1 - 5 on human Jurkat (human T-cell lymphoma) and HeLa (epithelial carcinoma) cell lines, where diterpene 3 exhibited activity in Jurkat cell lines after 48 h, with an IC 50 of 15.21 ± 1.0 µM. Molecular docking and dynamic simulations revealed a robust interaction between compound 3 and Hsp70 key residues.
Keyphrases
- heat shock protein
- molecular docking
- density functional theory
- heat shock
- endothelial cells
- molecular dynamics
- high resolution
- magnetic resonance
- mass spectrometry
- healthcare
- induced pluripotent stem cells
- oxidative stress
- systematic review
- solid state
- ms ms
- molecular dynamics simulations
- climate change
- liquid chromatography
- high performance liquid chromatography
- pluripotent stem cells
- tandem mass spectrometry
- binding protein
- human health
- single cell
- anti inflammatory
- risk assessment
- simultaneous determination
- electronic health record
- cell proliferation
- high speed
- cell death
- african american