[Retracted] (5E,7E)‐4,5,6 Trihydroxy‐3‐(hydroxymethyl)tetrahydro‐2H‐pyran‐2‐ylheptadeca‐5,7‐dienoate from Euclea crispa (L.) Inhibits Ovarian Cancer Cell Growth by Controlling Apoptotic and Metastatic Signaling Mechanisms
Author(s) -
Chella Perumal Palanisamy,
Bo Cui,
Hongxia Zhang,
Selvaraj Jayaraman,
Ponnulakshmi Rajagopal,
Vishnu Priya Veeraraghavan
Publication year - 2022
Publication title -
bioinorganic chemistry and applications
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.865
H-Index - 35
eISSN - 1565-3633
pISSN - 1687-479X
DOI - 10.1155/2022/4464056
Subject(s) - chemistry , hydroxymethyl , pyran , apoptosis , lead compound , stereochemistry , protein kinase b , in vivo , cancer research , biochemistry , in vitro , biology , microbiology and biotechnology
Bioactive compound (5E,7E)-4,5,6 trihydroxy-3-(hydroxymethyl)tetrahydro-2H-pyran-2-ylheptadeca-5,7-dienoate (compound 2) was isolated from Euclea crispa (E. crispa) by the chromatographic methods. Further, the compound was confirmed by spectroscopic techniques such as ultraviolet-visible (UV/Vis) spectrometer, Fourier transform infrared (FTIR) spectrometer, and 1H and 13C nuclear magnetic resonance (NMR). Compound 2 exhibited a significant antioxidant activity with IC50 values. It restrained the auxesis of HO-8910 cells in a shot-dependent mode. CXCR4, HER2, and Akt proteins involved in cell proliferation and metastasis were found to be significantly reduced ( p < 0.05 ). The protein that is responsible for the death of cells (Bcl-2 and Bcl-xL) was reduced ( p < 0.05 ), while the protein expression of p53 and caspase-9 was increased ( p < 0.05 ) in compound 2-treated HO-8910 cells. The results of molecular docking analysis showed the binding affinity with CXCR4 and HER2. Thus, compound 2 can serve as a promising chemotherapeutic agent for the intervention of ovarian cancer. The findings of this study conclude that compound 2 from E. crispa might work as a potential antioxidative and chemotherapeutic agent. The in vivo studies and attempts will pave way for this compound to be an effective drug hereafter.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom