Abstract
Hepatocellular carcinoma (HCC) is the most common liver cancer and a major cause of adult death. The current treatments for HCC suffer from drug resistance and poor prognosis; therefore, novel therapeutic agents are urgently needed. Phytochemicals have been proposed to treat a range of cancers. Among them, α-lipoic acid (α-LA), a naturally synthesized antioxidant found in various dietary animal and plant sources, prevents oxidant-mediated cell death in normal cells while inducing apoptosis in several cancer cell lines. Previously, we demonstrated that the treatment of hepatoma cells with α-LA induced apoptosis, which was preceded by the generation of reactive oxygen species (ROS) and activation of the p53 protein, a known inducer of mitochondria-mediated apoptosis. Several studies have shown that ROS-induced apoptosis is associated with endoplasmic reticulum (ER) stress and Unfolded Protein Response (UPR) activation. Herein, we investigated if α-LA-induced apoptosis in hepatoma cell lines was ER stress- and UPR-mediated by gene expression profiling analyses. UPR and ER stress pathways were the most up-regulated after treatment with α-LA. This finding, which has been confirmed by expression analyses of ER- and UPR-associated proteins, provides a better understanding of the molecular mechanisms behind the anti-tumoral action of α-LA on hepatoma cells.
Highlights
Hepatocellular carcinoma (HCC) is the most frequent and deadliest primary hepatic carcinoma worldwide[1,2]
In order to investigate the possible involvement of these pathways in α-Lipoic acid (α-LA)-induced apoptosis, gene expression profiling was performed on FaO cells treated from 6 up to 72 hours with 500 μM α-LA, by Illumina microarray
Increased intracellular Reactive Oxygen Species (ROS) levels have been associated to activation of Endoplasmic reticulum (ER) stress and Unfolded Protein Response (UPR) pathways which, due to the cell death inducing effect associated to their prolonged activation, have been regarded as potential anticancer targets[47,48]
Summary
Hepatocellular carcinoma (HCC) is the most frequent and deadliest primary hepatic carcinoma worldwide[1,2]. Data obtained have shown that α-LA was able to induce modifications in the gene and protein expression of the principal regulators of UPR and ER stress response[25,26,27,28], such as Protein Disulfide Isomerase (PDI)[29] and the ER stress sensors PKR-like ER Kinase (PERK)[30,31], Inositol-requiring enzyme 1 alpha (IRE1)[30,32] and Activation transcription factor 6 (ATF6)[30,33] In both cell lines the loss of viability was preceded by activation of the ER-related pro-apoptotic gene C/EBP Homologues Protein/DNA Damage Inducible Transcription 3 (GADD153/CHOP)[30]. Our results have provided evidence that α-LA induces apoptosis in hepatoma cells by triggering chronic ER stress and UPR response
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