4.6 Article

The Essential Oil from Oliveria decumbens Vent. (Apiaceae) as Inhibitor of Breast Cancer Cell (MCF-7) Growth

Journal

PHARMACEUTICALS
Volume 16, Issue 1, Pages -

Publisher

MDPI
DOI: 10.3390/ph16010059

Keywords

breast cancer; PTEN protein; Aurora kinase A; essential oil; apoptosis; Oliveria decumbens

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Oliveria decumbens Vent. is a traditional aromatic and medicinal plant used in Iran for various ailments including infections, gastrointestinal diseases, cancer, and inflammation. This study investigated the pharmacological potential of its essential oil (OEO) and its main compounds, particularly in relation to its cytotoxic effects on MCF-7 breast cancer cells. The results showed that OEO could inhibit cell growth, activate apoptosis, and enhance tumor suppression through the activation of specific genes. Molecular docking studies also revealed the potential of OEO's main compounds to target specific proteins involved in cancer growth. These findings suggest that OEO has promising potential as a cancer therapy agent in the pharmaceutical industry.
Oliveria decumbens Vent. is an aromatic and medicinal plant traditionally used in Iran for the treatment of infections, gastrointestinal diseases, cancer, and inflammation. This research was aimed at investigating the pharmacological potential of O. decumbens essential oil (OEO) and its main compounds, focusing on OEO's cytotoxic effects on MCF-7 breast cancer cells. OEO was obtained by hydro-distillation, and the chemical constituents were identified using GC-MS. Thymol, carvacrol, gamma-terpinene, and p-cymene were the main OEO constituents. When MCF-7 cells were treated with OEO, the expressions of genes related to apoptosis (BIM and Bcl-2), tumor suppression (PTEN), and cell growth inhibition (AURKA), were evaluated using real-time PCR. Moreover, molecular docking was used for studying in silico the interaction of OEO principal compounds with PTEN and AURKA. The expression of AURKA was significantly reduced since the OEO treatment enhanced the expression of PTEN. Through in silico molecular docking, it was revealed that thymol, carvacrol, p-cymene, and gamma-terpinene can activate PTEN and thus inhibit AURKA. Additionally, the DNA fragmentation assay, acridine orange/ethidium bromide (AO/EB) double-staining assay, and real-time PCR highlighted the fact that the OEO treatment could activate apoptosis and inhibit cell proliferation. Therefore, OEO is a viable candidate to be employed in the pharmaceutical industry, specifically as a possible agent for cancer therapy.

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