AI Article Synopsis

  • - Hepatocellular carcinoma (HCC) is a major form of liver cancer, with early-stage treatment options like surgery and transplantation, while advanced stages often require systemic therapies that can have significant side effects.
  • - The study investigates the effects of delta-tocotrienol (δ-TT) on HCC cells, particularly its role in inducing apoptosis, oxidative stress, and autophagy mechanisms within the HepG2 cell line.
  • - Findings suggest that δ-TT promotes cell death in HCC by inducing mitochondrial dysfunction and selective autophagy, which could be harnessed as a new treatment strategy for advanced HCC.

Article Abstract

(1) Hepatocellular carcinoma (HCC) is the predominant form of primary liver cancer. Surgical resection, tumor ablation, and liver transplantation are curative treatments indicated for early-stage HCC. The management of intermediate and advanced stages of pathology is based on the use of systemic therapies which often show important side effects. Vitamin E-derivative tocotrienols (TTs) play antitumoral properties in different tumors. Here, we analyzed the activity of delta-TT (δ-TT) on HCC human cell lines. (2) We analyzed the ability of δ-TT to trigger apoptosis, to induce oxidative stress, autophagy, and mitophagy in HepG2 cell line. We evaluated the correlation between the activation of autophagy with the ability of δ-TT to induce cell death. (3) The data obtained demonstrate that δ-TT exerts an antiproliferative and proapoptotic effect in HCC cells. Furthermore, δ-TT induces the release of mitochondrial ROS and causes a structural and functional alteration of the mitochondria compatible with a fission process. Finally, δ-TT triggers selective autophagy process removing dysfunctional mitochondria. Inhibition of autophagy reversed the cytotoxic action of δ-TT. (4) Our results demonstrate that δ-TT through the activation of autophagy could represent a potential new approach in the treatment of advanced HCC.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11311296PMC
http://dx.doi.org/10.3390/cancers16152654DOI Listing

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