1. Academic Validation
  2. Anti-cancer mechanisms of linalool and 1,8-cineole in non-small cell lung cancer A549 cells

Anti-cancer mechanisms of linalool and 1,8-cineole in non-small cell lung cancer A549 cells

  • Heliyon. 2020 Dec 15;6(12):e05639. doi: 10.1016/j.heliyon.2020.e05639.
Boris Rodenak-Kladniew 1 2 María Agustina Castro 1 Rosana Crespo 3 Marianela Galle 1 2 Margarita García de Bravo 1
Affiliations

Affiliations

  • 1 Instituto de Investigaciones Bioquímicas de La Plata (INIBIOLP), CONICET-UNLP, CCT-La Plata La Plata, Argentina.
  • 2 Cátedra de Biología, Facultad de Ciencias Médicas, Universidad Nacional de La Plata, La Plata, Argentina.
  • 3 Universidad Nacional de Córdoba, Facultad de Ciencias Químicas, Departamento de Farmacología, Instituto de Farmacología Experimental Córdoba (IFEC-CONICET), Córdoba, Argentina.
Abstract

Linalool and 1,8-cineole are plant-derived isoprenoids with Anticancer activities in lung Cancer cells, nevertheless, the cellular and molecular mechanisms of action remain poorly understood. The purpose of this study was to determine the Anticancer mechanisms of action of linalool and 1,8-cineole in lung adenocarcinoma A549 cells. Linalool (0-2.0 mM) and 1,8-cineole (0-8.0 mM) inhibited cell proliferation by inducing G0/G1 and/or G2/M cell cycle arrest without affecting cell viability of normal lung WI-38 cells. None of the two monoterpenes were able to induce Apoptosis, as observed by the lack of Caspase-3 and caspase-9 activation, PARP cleavage, and DNA fragmentation. Linalool, but not 1,8-cineole, increased Reactive Oxygen Species production and mitochondrial membrane potential depolarization. Reactive Oxygen Species were involved in cell growth inhibition and mitochondrial depolarization induced by linalool since the antioxidant N-acetyl-L-cysteine prevented both effects. Besides, linalool (2.0 mM) and 1,8-cineole (8.0 mM) inhibited A549 cell migration. The combination of each monoterpene with simvastatin increased the G0/G1 cell cycle arrest and sensitized cells to Apoptosis compared with simvastatin alone. Our results showed that both monoterpenes might be promising Anticancer agents with antiproliferative, anti-metastatic, and sensitizer properties for lung Cancer therapy.

Keywords

1,8-Cineole; Bioactive plant product; Biochemistry; Cancer research; Cell biology; Cell culture; Cell migration; Chemosensitizers; Chemotherapy; Cytostatic effects; Cytotoxicity; Linalool; Natural product; Non-small lung cancer cells; Oxidative stress; Pharmaceutical science; Reactive oxygen species.

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