Shaji Unnikrishnan Paruthiyezhath, Tuti Nikhil, Das Susmita, Anindya Roy, Mohan Monisha
Department of Biotechnology, Indian Institute of Technology Hyderabad, Kandi Sanga Reddy, Telangana, 502284, India.
Department of Science and Humanities, Indian Institute of Information Technology Design and Manufacturing Kancheepuram, Chennai, Tamilnadu, 600127, India.
Mol Divers. 2023 Apr;27(2):931-938. doi: 10.1007/s11030-022-10444-2. Epub 2022 May 11.
The human DNA repair enzyme AlkB homologue-2 (ALKBH2) repairs methyl adducts from genomic DNA. Overexpression of ALKBH2 has been implicated in both tumorigenesis and chemotherapy resistance in some cancers, including glioblastoma and renal cancer rendering it a potential therapeutic target and a diagnostic marker. However, no inhibitor is available against these important DNA repair proteins. Intending to repurpose a drug as an inhibitor of ALKBH2, we performed in silico evaluation of HIV protease inhibitors and identified Ritonavir as an ALKBH2-interacting molecule. Using molecular dynamics simulation, we elucidated the molecular details of Ritonavir-ALKBH2 interaction. The present work highlights that Ritonavir might be used to target the ALKBH2-mediated DNA alkylation repair.
人类DNA修复酶AlkB同源物2(ALKBH2)可修复基因组DNA中的甲基加合物。在包括胶质母细胞瘤和肾癌在内的某些癌症中,ALKBH2的过表达与肿瘤发生和化疗耐药性均有关联,这使其成为一个潜在的治疗靶点和诊断标志物。然而,目前尚无针对这些重要DNA修复蛋白的抑制剂。为了将一种药物重新用作ALKBH2的抑制剂,我们对HIV蛋白酶抑制剂进行了计算机模拟评估,并确定利托那韦是一种与ALKBH2相互作用的分子。通过分子动力学模拟,我们阐明了利托那韦与ALKBH2相互作用的分子细节。目前的研究突出表明,利托那韦可能用于靶向ALKBH2介导的DNA烷基化修复。