Lei Yuchen, Klionsky Daniel J
Life Sciences Institute and Department of Molecular, Cellular and Developmental Biology, University of Michigan, Ann Arbor, MI, USA.
Autophagy. 2025 Mar;21(3):497-499. doi: 10.1080/15548627.2024.2434784. Epub 2024 Dec 15.
Type I topoisomerases (TOP1) are critical to remove the topological stress when DNA double strands are unwound. The TOP1 cleavage complexes (TOP1cc) are normally transient, and the stabilization of TOP1cc by its inhibitors, such as camptothecin (CPT), may lead to DNA damage and become cytotoxic. The proteasome pathway degrades trapped TOP1, which is necessary for the repair machinery to gain access to the DNA; however, this process is mainly described when the CPT concentration is high, at levels which are clinically unachievable. In a recently published study, Lascaux et al. identify macroautophagy/autophagy as a new pathway to remove DNA lesions upon clinically relevant low-dose CPT treatment. The autophagy receptor TEX264 binds to TOP1 and brings this protein and its bound DNA fragments to the phagophore; subsequently, they are ultimately delivered to the lysosome for degradation. This study demonstrates the role of autophagy in maintaining genome stability from a new perspective and reveals potential targets to deal with the resistance to TOP1cc inhibitors during cancer treatment.
I型拓扑异构酶(TOP1)对于在DNA双链解开时消除拓扑应力至关重要。TOP1切割复合物(TOP1cc)通常是短暂的,其抑制剂(如喜树碱,CPT)对TOP1cc的稳定作用可能导致DNA损伤并具有细胞毒性。蛋白酶体途径降解被困的TOP1,这对于修复机制接触DNA是必要的;然而,这一过程主要是在CPT浓度很高(临床无法达到的水平)时描述的。在最近发表的一项研究中,拉斯科等人确定巨自噬/自噬是在临床相关低剂量CPT治疗后消除DNA损伤的新途径。自噬受体TEX264与TOP1结合,并将该蛋白及其结合的DNA片段带到吞噬泡;随后,它们最终被输送到溶酶体进行降解。这项研究从一个新的角度证明了自噬在维持基因组稳定性中的作用,并揭示了在癌症治疗期间应对TOP1cc抑制剂耐药性的潜在靶点。