Bonora Massimo, Pinton Paolo
Section of Pathology, Oncology and Experimental Biology, Laboratory for Technologies of Advanced Therapies (LTTA), Department of Morphology, Surgery and Experimental Medicine, University of Ferrara , Ferrara , Italy.
Front Oncol. 2014 Nov 17;4:302. doi: 10.3389/fonc.2014.00302. eCollection 2014.
Since its discovery in the 1970s, the mitochondrial permeability transition (MPT) has been proposed to be a strategic regulator of cell death. Intense research efforts have focused on elucidating the molecular components of the MPT because this knowledge may help to better understand and treat various pathologies ranging from neurodegenerative and cardiac diseases to cancer. In the case of cancer, several studies have revealed alterations in the activity of the mitochondrial permeability transition pore (mPTP) and have determined its regulatory mechanism; these studies have also suggested that suppression of the activity of the mPTP, rather than its inactivation, commonly occurs in solid neoplasms. This review focuses on the most recent advances in understanding mPTP regulation in cancer and highlights the ability of the mPTP to impede the mechanisms of cell death.
自20世纪70年代被发现以来,线粒体通透性转换(MPT)被认为是细胞死亡的一个关键调节因子。大量研究致力于阐明MPT的分子组成部分,因为这些知识有助于更好地理解和治疗从神经退行性疾病、心脏疾病到癌症等各种病症。就癌症而言,多项研究揭示了线粒体通透性转换孔(mPTP)活性的改变,并确定了其调控机制;这些研究还表明,在实体瘤中,通常发生的是mPTP活性的抑制而非失活。本综述聚焦于癌症中mPTP调控的最新进展,并强调了mPTP阻碍细胞死亡机制的能力。