Carafa Vincenzo, Russo Rosita, Della Torre Laura, Cuomo Francesca, Dell'Aversana Carmela, Sarno Federica, Sgueglia Giulia, Di Donato Marzia, Rotili Dante, Mai Antonello, Nebbioso Angela, Cobellis Gilda, Chambery Angela, Altucci Lucia
Dipartimento di Medicina di Precisione, Università degli Studi della Campania "Luigi Vanvitelli", Naples, Italy.
Dipartimento di Scienze e Tecnologie Ambientali Biologiche e Farmaceutiche, Università degli Studi della Campania "Luigi Vanvitelli", Caserta, Italy.
Front Oncol. 2020 May 21;10:820. doi: 10.3389/fonc.2020.00820. eCollection 2020.
The involvement of sirtuins (SIRTs) in modulating metabolic and stress response pathways is attracting growing scientific interest. Some SIRT family members are located in mitochondria, dynamic organelles that perform several crucial functions essential for eukaryotic life. Mitochondrial dysfunction has emerged as having a key role in a number of human diseases, including cancer. Here, we investigated mitochondrial damage resulting from treatment with a recently characterized pan-SIRT inhibitor, MC2494. MC2494 was able to block mitochondrial biogenesis and function in terms of ATP synthesis and energy metabolism, suggesting that it might orchestrate cell response to metabolic stress and thereby interfere with cancer promotion and progression. Targeting mitochondrial function could thus be considered a potential anticancer strategy for use in clinical therapy.
沉默调节蛋白(SIRTs)参与调节代谢和应激反应途径,正吸引着越来越多的科学关注。一些SIRT家族成员位于线粒体中,线粒体是具有动态变化的细胞器,执行着真核生物生命所必需的若干关键功能。线粒体功能障碍已被证明在包括癌症在内的多种人类疾病中起关键作用。在此,我们研究了用一种最近鉴定出的泛SIRT抑制剂MC2494处理后导致的线粒体损伤。MC2494能够在ATP合成和能量代谢方面阻断线粒体生物发生和功能,这表明它可能协调细胞对代谢应激的反应,从而干扰癌症的发生和进展。因此,靶向线粒体功能可被视为一种潜在的用于临床治疗的抗癌策略。