Tragia plukenetii-Assisted Omega-Decenol as Potential Anticancer Agent: its Isolation, Characterization, and Validation.
Sowmya Priya ManoharanSangilimuthu Alagar YadavBalamurugan PandiyanGnanaselvan SuvathikaPublished in: Applied biochemistry and biotechnology (2022)
The second most common and lethal disease is lung cancer. To combat the negative effects of today's synthetic medications, natural phytomedicines are required. Tragia plukenetii is a medicinal plant native to India that belongs to the Euphorbiaceae family. The purpose of this research is to isolate bioactive compounds from T. plukenetii leaves and then test them for anticancer property. A single compound (CH: ME-20:80) was separated using TLC, and an RF value of 0.55 was determined. Spectral analyses utilizing UV-Visible Spectrophotometer and FT-IR were used to examine the absorbance and functional groups. 13 C-NMR and 1 H-NMR studies revealed the tentative name of the purified phytochemical as omega-decenol (OD). Further antioxidant and anticancer properties of OD were tested for in vitro. In comparison to conventional L-ascorbic acid, the DPPH radical scavenging assay experiment yielded an IC 50 of 147.48 g/ml. With an IC 50 value of 24 µg/ml (Omega-decenol) and 32 µg/ml (doxorubicin), the MTT assay demonstrated the cytotoxic capability against the A549 lung cancer cell line. FACS revealed the cell cycle arrest of A549 at S phase compared to control with the high-dose IC 50 (250 µg/ml) of omega-decenol. Twelve major compounds were detected in the active fraction using GC-MS analysis, where n-hexadecanoic acid was found as a major. Omega-decenol showed good binding affinity against EGFR, amongst other receptors in the in silico docking study. This research reveals the potent anticancer activity of the isolated compound omega-decenol from T. plukenetii leaves and provides a key path to understanding the molecular interaction in anticancer aspects against adenocarcinoma.
Keyphrases
- high dose
- cell cycle arrest
- magnetic resonance
- high resolution
- high throughput
- single cell
- low dose
- cell death
- tyrosine kinase
- molecular dynamics
- magnetic resonance imaging
- epidermal growth factor receptor
- radiation therapy
- oxidative stress
- cell proliferation
- solid state
- climate change
- drug delivery
- molecular dynamics simulations
- single molecule
- risk assessment
- rectal cancer
- clinical evaluation