dc.creatorRodenak Kladniew, Boris Emilio
dc.creatorCastro, Maria Agustina
dc.creatorStärkel, Peter
dc.creatorGalle, Marianela Edith
dc.creatorCrespo, Rosana
dc.date.accessioned2021-10-14T17:20:25Z
dc.date.accessioned2022-10-15T07:57:45Z
dc.date.available2021-10-14T17:20:25Z
dc.date.available2022-10-15T07:57:45Z
dc.date.created2021-10-14T17:20:25Z
dc.date.issued2020-02-15
dc.identifierRodenak 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.identifier0024-3205
dc.identifierhttp://hdl.handle.net/11336/143644
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4363021
dc.description.abstractAims: 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.languageeng
dc.publisherElsevier Inc
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://linkinghub.elsevier.com/retrieve/pii/S0024320520300187
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.lfs.2020.117271
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subject1,8-CINEOLE
dc.subjectAKT/MTOR
dc.subjectAMPK
dc.subjectCELL CYCLE ARREST
dc.subjectHEPATOCELLULAR CARCINOMA CELLS
dc.subjectMAPKS
dc.subjectOXIDATIVE STRESS
dc.subjectSENESCENCE
dc.title1,8-Cineole promotes G0/G1 cell cycle arrest and oxidative stress-induced senescence in HepG2 cells and sensitizes cells to anti-senescence drugs
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/publishedVersion


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