1. Academic Validation
  2. α-Lipoic acid induces Endoplasmic Reticulum stress-mediated apoptosis in hepatoma cells

α-Lipoic acid induces Endoplasmic Reticulum stress-mediated apoptosis in hepatoma cells

  • Sci Rep. 2020 Apr 28;10(1):7139. doi: 10.1038/s41598-020-64004-5.
Monica Pibiri 1 Pia Sulas 1 Tania Camboni 2 Vera Piera Leoni 1 Gabriella Simbula 3
Affiliations

Affiliations

  • 1 Department of Biomedical Sciences, Unit of Oncology and Molecular Pathology, University of Cagliari, Cagliari, Italy.
  • 2 National Research Council, Institute of Biomedical Technologies, Segrate, Milano, Italy.
  • 3 Department of Biomedical Sciences, Unit of Oncology and Molecular Pathology, University of Cagliari, Cagliari, Italy. [email protected].
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.

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