Trotta Andrew Paul, Chipuk Jerry Edward
Department of Oncological Sciences, Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Place, Box 1130, New York, NY, 10029, USA.
The Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Place, Box 1130, New York, NY, 10029, USA.
Cell Mol Life Sci. 2017 Jun;74(11):1999-2017. doi: 10.1007/s00018-016-2451-3. Epub 2017 Jan 12.
Mitochondria are dynamic organelles that supply energy required to drive key cellular processes, such as survival, proliferation, and migration. Critical to all of these processes are changes in mitochondrial architecture, a mechanical mechanism encompassing both fusion and fragmentation (fission) of the mitochondrial network. Changes to mitochondrial shape, size, and localization occur in a regulated manner to maintain energy and metabolic homeostasis, while deregulation of mitochondrial dynamics is associated with the onset of metabolic dysfunction and disease. In cancers, oncogenic signals that drive excessive proliferation, increase intracellular stress, and limit nutrient supply are all able to alter the bioenergetic and biosynthetic requirements of cancer cells. Consequently, mitochondrial function and shape rapidly adapt to these hostile conditions to support cancer cell proliferation and evade activation of cell death programs. In this review, we will discuss the molecular mechanisms governing mitochondrial dynamics and integrate recent insights into how changes in mitochondrial shape affect cellular migration, differentiation, apoptosis, and opportunities for the development of novel targeted cancer therapies.
线粒体是动态细胞器,可提供驱动关键细胞过程所需的能量,如细胞存活、增殖和迁移。线粒体结构的变化对所有这些过程都至关重要,线粒体结构是一种机械机制,包括线粒体网络的融合和分裂(裂变)。线粒体的形状、大小和定位变化以一种受调控的方式发生,以维持能量和代谢稳态,而线粒体动力学失调与代谢功能障碍和疾病的发生有关。在癌症中,驱动过度增殖、增加细胞内应激和限制营养供应的致癌信号都能够改变癌细胞的生物能量和生物合成需求。因此,线粒体功能和形状会迅速适应这些不利条件,以支持癌细胞增殖并逃避细胞死亡程序的激活。在这篇综述中,我们将讨论控制线粒体动力学的分子机制,并整合最近对线粒体形状变化如何影响细胞迁移、分化、凋亡以及新型靶向癌症治疗发展机会的见解。