Department of Orthopedics, The Second Affiliated Hospital of Nanjing Medical University, Nanjing, 210011, Jiangsu, People's Republic of China.
Department of Orthopedics, Sir Run Run Hospital, Nanjing Medical University, Nanjing, 210011, Jiangsu, People's Republic of China.
Sci Rep. 2024 Feb 13;14(1):3577. doi: 10.1038/s41598-024-54197-4.
Osteosarcoma (OS) is the most common primary malignant tumor of bone. Remodelin, an inhibitor of the N (4)-Acetylcytidine (ac4C) acetylation modifying enzyme N-acetyltransferase 10 (NAT10), has been shown to have therapeutic effects on cancer in several studies, and our previous studies have confirmed the inhibitory effect of Remodelin on OS cells, however, the mechanism of action has not yet been elucidated. We used network pharmacological analysis to quantify the therapeutic targets of Remodelin against OS. acRIP-seq and RNA-seq were performed to investigate the inhibitory activity of Remodelin on acetylation and its effect on the transcriptome after intervening in OS cells U2OS with Remodelin in vitro. Key target genes were deduced based on their pharmacological properties, combined with network pharmacology results and sequencing results. Finally, the deduced target genes were validated with vitro experiments. Network pharmacological analysis showed that 2291 OS-related target genes and 369 Remodelin-related target genes were obtained, and 116 overlapping genes were identified as Remodelin targets for OS treatment. Sequencing results showed that a total of 13,736 statistically significant ac4C modification peaks were detected by acRIP-seq, including 6938 hypoacetylation modifications and 6798 hyperacetylation modifications. A total of 2350 statistically significant mRNAs were detected by RNA-seq, of which 830 were up-regulated and 1520 were down-regulated. Association analyses identified a total of 382 genes that were Hypoacetylated-down, consistent with inhibition of mRNA acetylation and expression by Remodelin. Five genes, CASP3, ESR2, FGFR2, IGF1 and MAPK1, were identified as key therapeutic targets of Remodelin against OS. Finally, in vitro experiments, CCK-8 and qRT-PCR demonstrated that Remodelin indeed inhibited the proliferation of OS cells and reduced the expression of three genes: ESR2, IGF1, and MAPK1. In conclusion, ESR2, IGF1 and MAPK1 were identified as key therapeutic targets of Remodelin against OS. This reveals the target of Remodelin's pharmacological action on OS and provides new ideas for the treatment of OS.
骨肉瘤(OS)是最常见的原发性骨恶性肿瘤。重塑酶是 N(4)-乙酰胞嘧啶(ac4C)乙酰化修饰酶 N-乙酰转移酶 10(NAT10)的抑制剂,几项研究表明其对癌症具有治疗作用,我们之前的研究也证实了重塑酶对 OS 细胞的抑制作用,但是其作用机制尚未阐明。我们使用网络药理学分析来量化重塑酶对 OS 的治疗靶点。进行 acRIP-seq 和 RNA-seq 以研究重塑酶在体外干预 OS 细胞 U2OS 时对乙酰化的抑制活性及其对转录组的影响。根据其药理学特性,结合网络药理学结果和测序结果,推断出关键靶基因。最后,通过体外实验验证了推断出的靶基因。网络药理学分析显示,获得了 2291 个与 OS 相关的靶基因和 369 个与重塑酶相关的靶基因,鉴定出 116 个重叠基因作为重塑酶治疗 OS 的靶基因。测序结果显示,通过 acRIP-seq 共检测到 13736 个统计学上显著的 ac4C 修饰峰,包括 6938 个低乙酰化修饰峰和 6798 个高乙酰化修饰峰。通过 RNA-seq 共检测到 2350 个统计学上显著的 mRNA,其中 830 个上调,1520 个下调。关联分析共鉴定出 382 个 Hypoacetylated-down 基因,与重塑酶抑制 mRNA 乙酰化和表达一致。CASP3、ESR2、FGFR2、IGF1 和 MAPK1 这 5 个基因被确定为重塑酶治疗 OS 的关键治疗靶点。最后,体外实验 CCK-8 和 qRT-PCR 表明,重塑酶确实抑制了 OS 细胞的增殖,并降低了三个基因的表达:ESR2、IGF1 和 MAPK1。总之,ESR2、IGF1 和 MAPK1 被鉴定为重塑酶治疗 OS 的关键治疗靶点。这揭示了重塑酶对 OS 药理作用的靶点,为 OS 的治疗提供了新的思路。