dc.creator | Rodenak Kladniew, Boris Emilio | |
dc.creator | Castro, Maria Agustina | |
dc.creator | Stärkel, Peter | |
dc.creator | Galle, Marianela Edith | |
dc.creator | Crespo, Rosana | |
dc.date.accessioned | 2021-10-14T17:20:25Z | |
dc.date.accessioned | 2022-10-15T07:57:45Z | |
dc.date.available | 2021-10-14T17:20:25Z | |
dc.date.available | 2022-10-15T07:57:45Z | |
dc.date.created | 2021-10-14T17:20:25Z | |
dc.date.issued | 2020-02-15 | |
dc.identifier | Rodenak Kladniew, Boris Emilio; Castro, Maria Agustina; Stärkel, Peter; Galle, Marianela Edith; Crespo, Rosana; 1,8-Cineole promotes G0/G1 cell cycle arrest and oxidative stress-induced senescence in HepG2 cells and sensitizes cells to anti-senescence drugs; Elsevier Inc; Life Sciences; 243; 15-2-2020; 1-13 | |
dc.identifier | 0024-3205 | |
dc.identifier | http://hdl.handle.net/11336/143644 | |
dc.identifier | CONICET Digital | |
dc.identifier | CONICET | |
dc.identifier.uri | https://repositorioslatinoamericanos.uchile.cl/handle/2250/4363021 | |
dc.description.abstract | Aims: 1,8-Cineole is a plant-derived monoterpene and a major constituent of Eucalyptus essential oil. Previously, we demonstrated that 1,8-cineole inhibited hepatocellular carcinoma (HCC) HepG2 cell growth. However, the underlying mechanisms remain unknown. Here, we evaluated the mechanisms of action of 1,8-cineole and the potential benefits of its combination with anticancer compounds harboring “anti-senescence” properties in HepG2 cells. Main methods: Cell viability was determined by the MTT assay. Cell cycle was assessed through flow cytometry (FC) and western blot (WB). Senescence was determined by the SA-β-galactosidase assay, and apoptosis by caspase-3 activity, WB, and TUNEL. MAPKs (ERK, JNK, and p38), AMPK, and Akt/mTOR were analyzed by WB. Reactive oxygen species (ROS) and mitochondrial membrane potential (ΔΨm) were evaluated by FC and fluorescence microscopy. Key findings: 1,8-Cineole inhibited cell proliferation by promoting G0/G1 arrest. While 1,8-cineole was unable to trigger apoptosis, it induced cellular senescence. 1,8-Cineole promoted ROS production, ΔΨm depolarization, AMPK, ERK, and p38 activation and mTOR inhibition. Antioxidants, like N-acetyl-L-cysteine and vitamins, prevented HepG2 cell growth inhibition and senescence induced by 1,8-cineole. Pre-incubation with 1,8-cineole sensitized HepG2 cells to the anti-senescence compounds, quercetin, simvastatin, U0126, and SB202190. Combinations of 1,8-cineole and each compound synergistically inhibited cell viability, and combined treatment with 1,8-cineole and simvastatin induced apoptosis. Significance: 1,8-Cineole induces G0/G1 arrest and senescence in HepG2 cells through oxidative stress and MAPK, AMPK, and Akt/mTOR pathways, and sensitizes cells to anti-senescence drugs, suggesting that 1,8-cineole has potential as an antineoplastic and adjuvant compound in combination with anti-senescence drugs in HCC therapy. | |
dc.language | eng | |
dc.publisher | Elsevier Inc | |
dc.relation | info:eu-repo/semantics/altIdentifier/url/https://linkinghub.elsevier.com/retrieve/pii/S0024320520300187 | |
dc.relation | info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.lfs.2020.117271 | |
dc.rights | https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ | |
dc.rights | info:eu-repo/semantics/restrictedAccess | |
dc.subject | 1,8-CINEOLE | |
dc.subject | AKT/MTOR | |
dc.subject | AMPK | |
dc.subject | CELL CYCLE ARREST | |
dc.subject | HEPATOCELLULAR CARCINOMA CELLS | |
dc.subject | MAPKS | |
dc.subject | OXIDATIVE STRESS | |
dc.subject | SENESCENCE | |
dc.title | 1,8-Cineole promotes G0/G1 cell cycle arrest and oxidative stress-induced senescence in HepG2 cells and sensitizes cells to anti-senescence drugs | |
dc.type | info:eu-repo/semantics/article | |
dc.type | info:ar-repo/semantics/artículo | |
dc.type | info:eu-repo/semantics/publishedVersion | |