Bioactive compound 1,8-Cineole selectively induces G2/M arrest in A431 cells through the upregulation of the p53 signaling pathway and molecular docking studies

Article ID	Journal	Published Year	Pages	File Type
8518047	Phytomedicine	2018	40 Pages	PDF

Keywords

ADT ATG ΔΨm DAPI cyt-c Autodock Tools Bcl-2 TLC Beclin-1 NMA HaCaT PARP1 p53 A431 FBS DMEM DOX FACS nuclear magnetic resonance 1,8-Cineole 4′,6-diamidino-2-phenylindole DMSO DNA GC–MS Dulbecco's modified Eagle's medium MTT ROS Alamar Blue deoxyribonucleic acid Tem Bax Fourier transform infrared NMR Cell cycle arrest Apoptosis fluorescence-activated cell sorting Doxorubicin Dimethyl sulfoxide fetal bovine serum cytochrome c FTIR Gas Chromatography Mass Spectrometry B-cell lymphoma 2 Mitochondria Transmission electron microscope Mitochondrial membrane potential Tumor suppressor protein Propidium iodide autophagy-related genes skin carcinoma Human keratinocytes thin layer chromatography caspase Reactive oxygen species

Related Topics

Life Sciences Biochemistry, Genetics and Molecular Biology Clinical Biochemistry

Bioactive compound 1,8-Cineole selectively induces G2/M arrest in A431 cells through the upregulation of the p53 signaling pathway and molecular docking studies

Authors

Sowndarya Sampath, Sangeetha Subramani, Sridevi Janardhanam, Preethi Subramani, Arun Yuvaraj, Rose Chellan,