Abstract
Lantana camara is an important medicinal plant that contains many active compounds, including pentacyclic triterpenoids, with numerous biological activities. The present study was conducted to evaluate the anti-oxidant, anti-tumour, and cell cycle arrest properties of chemical compounds extracted from L. camara leaves. Four compounds were identified after subjecting the plant methanolic extract to LC-MS/MS analysis: lantadene A, lantadene B, icterogenin, and lantadene C. Potential antioxidant activity was examined using 2, 2-diphenyl-1-picrylhydrazyl and compared with vitamin C as a control. Lantadene A and B were confirmed to possess the highest scavenging activity, while icterogenin and lantadene C exhibited a lesser antioxidant effect. All extracted compounds exerted a dose-dependent reduction in MCF-7 cell viability; however, lantadene B showed the highest anti-cancer activity, with an IC50 of 112.2 μg mL−1, and was therefore used in subsequent experiments. The results also confirmed the significant release of caspase 9 in a dose-dependent pattern following treatment of MCF-7 cells with a range of lantadene B concentrations. Lantadene B was found to induce MCF-7 cell cycle arrest in G1, blocking the G1/S transition with a maximum significant (p ≤ 0.01) cell count of 80.35% at 25 µg mL−1. No significant changes were observed in S phase, but a decrease in the MCF-7 population was exhibited in G2/M phase.
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The authors are grateful to the College of Biotechnology at Al-Naharin University for offering funding, space, and utilities to accomplish the project (Grant No. COB-85).
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A-SAZ and A-SAF designed the experiments; A-SAF and SZR were involved in performing the designed experiments; A-SAF and A-OJR were responsible for analysing the data and writing and approving the manuscript.
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Shamsee, Z.R., Al-Saffar, A.Z., Al-Shanon, A.F. et al. Cytotoxic and cell cycle arrest induction of pentacyclic triterpenoides separated from Lantana camara leaves against MCF-7 cell line in vitro. Mol Biol Rep 46, 381–390 (2019). https://doi.org/10.1007/s11033-018-4482-3
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DOI: https://doi.org/10.1007/s11033-018-4482-3