Sancho Sara Cuesta, Ouchi Toru
Department of Cancer Genetics, Roswell Park Cancer Institute, Buffalo, NY14263, USA.
Int J Cancer Res Mol Mech. 2015 Aug;1(2). doi: 10.16966/2381-3318.107. Epub 2015 Jul 2.
DNA damage is induced in many types of cells by internal and external cell stress. When DNA is damaged, DNA Damage Response (DDR) programs are activated to repair the DNA lesions in order to preserve genomic integrity and suppress subsequent malignant transformation. Among these programs is cell cycle checkpoint that ensures cell cycle arrest and subsequent repair of the damaged DNA, apoptosis and senescence in various phases of the cell cycle. Moreover, recent studies have established the cell differentiation checkpoint, the other type of the checkpoint that is specifically activated in the course of differentiation. We will discuss the evidences that support the link between DNA damage proteins and C2C12 cell differentiation.
DNA损伤可由内部和外部细胞应激在多种类型的细胞中诱导产生。当DNA受损时,DNA损伤反应(DDR)程序会被激活以修复DNA损伤,从而维持基因组完整性并抑制随后的恶性转化。这些程序包括细胞周期检查点,它可确保细胞周期停滞并随后修复受损DNA,以及细胞周期各阶段的凋亡和衰老。此外,最近的研究确立了细胞分化检查点,这是在分化过程中特异性激活的另一种检查点类型。我们将讨论支持DNA损伤蛋白与C2C12细胞分化之间联系的证据。