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TRAIL-Sensitizing Effects of Flavonoids in Cancer.
Luiz-Ferreira, Anderson; Pacifico, Teresa; Cruz, Álefe Cardoso; Laudisi, Federica; Monteleone, Giovanni; Stolfi, Carmine.
Afiliación
  • Luiz-Ferreira A; Inflammatory Bowel Disease Research Laboratory, Department of Biological Sciences, Institute of Biotechnology, Federal University of Catalão (UFCAT), Catalão 75704020, GO, Brazil.
  • Pacifico T; Department of Systems Medicine, University of Rome "Tor Vergata", 00133 Rome, Italy.
  • Cruz ÁC; Inflammatory Bowel Disease Research Laboratory, Department of Biological Sciences, Institute of Biotechnology, Federal University of Catalão (UFCAT), Catalão 75704020, GO, Brazil.
  • Laudisi F; Department of Systems Medicine, University of Rome "Tor Vergata", 00133 Rome, Italy.
  • Monteleone G; Department of Systems Medicine, University of Rome "Tor Vergata", 00133 Rome, Italy.
  • Stolfi C; Department of Systems Medicine, University of Rome "Tor Vergata", 00133 Rome, Italy.
Int J Mol Sci ; 24(23)2023 Nov 22.
Article en En | MEDLINE | ID: mdl-38068921
Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) represents a promising anticancer agent, as it selectively induces apoptosis in transformed cells without altering the cellular machinery of healthy cells. Unfortunately, the presence of TRAIL resistance mechanisms in a variety of cancer types represents a major hurdle, thus limiting the use of TRAIL as a single agent. Accumulating studies have shown that TRAIL-mediated apoptosis can be facilitated in resistant tumors by combined treatment with antitumor agents, ranging from synthetic molecules to natural products. Among the latter, flavonoids, the most prevalent polyphenols in plants, have shown remarkable competence in improving TRAIL-driven apoptosis in resistant cell lines as well as tumor-bearing mice with minimal side effects. Here, we summarize the molecular mechanisms, such as the upregulation of death receptor (DR)4 and DR5 and downregulation of key anti-apoptotic proteins [e.g., cellular FLICE-inhibitory protein (c-FLIP), X-linked inhibitor of apoptosis protein (XIAP), survivin], underlying the TRAIL-sensitizing properties of different classes of flavonoids (e.g., flavones, flavonols, isoflavones, chalcones, prenylflavonoids). Finally, we discuss limitations, mainly related to bioavailability issues, and future perspectives regarding the clinical use of flavonoids as adjuvant agents in TRAIL-based therapies.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Flavonoides / Neoplasias / Antineoplásicos Límite: Animals Idioma: En Revista: Int J Mol Sci Año: 2023 Tipo del documento: Article País de afiliación: Brasil Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Flavonoides / Neoplasias / Antineoplásicos Límite: Animals Idioma: En Revista: Int J Mol Sci Año: 2023 Tipo del documento: Article País de afiliación: Brasil Pais de publicación: Suiza