XRCC8突变引起对PARP抑制的超敏反应而没有同源重组修复缺陷

IF 1.5 4区 医学 Q4 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Mutation Research-Fundamental and Molecular Mechanisms of Mutagenesis Pub Date : 2023-01-01 DOI:10.1016/j.mrfmmm.2023.111815
Junko Maeda , Jeremy S. Haskins , Takamitsu A. Kato
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引用次数: 0

摘要

PARP抑制剂对同源重组(HR)修复缺陷细胞造成严重毒性,因为在DNA复制过程中缺乏HR修复的情况下,PARP抑制剂诱导的DNA损伤会导致致命的DNA双链断裂。PARP抑制剂是首个临床批准的用于合成致死性的药物。PARP抑制剂的合成致死相互作用并不局限于HR修复缺陷细胞。我们研究了从中国仓鼠肺源性V79细胞中分离的放射敏感性突变体,以在PARP抑制的背景下鉴定新的合成致死靶标。HR修复缺陷型BRCA2突变细胞用于阳性对照。在测试的细胞中,XRCC8突变体对PARP抑制剂奥拉帕尼表现出超敏反应。XRCC8突变体对博来霉素和喜树碱的敏感性与BRCA2突变体相似。XRCC8突变体在奥拉帕尼处理下表现出γ-H2AX病灶形成频率和S期依赖性染色体畸变的升高。观察到奥拉帕尼治疗后计数的损伤灶在XRCC8中与BRCA2突变体中一样升高。尽管这可能表明XRCC8在HR修复中在类似于BRCA2的DNA修复途径中发挥作用,但XRCC8突变体表现出功能性HR修复,包括正确的Rad51焦点形成,甚至在PARP抑制剂处理下提高姐妹染色单体交换频率。相比之下,在HR修复缺陷型BRCA2突变体中,RAD51病灶的形成受到抑制。此外,XRCC8突变体没有表现出PARP抑制剂延迟有丝分裂进入,而BRCA2突变体表现出。XRCC8突变细胞系先前已报道在ATM基因中具有突变。在测试的突变体和野生型细胞中,XRCC8突变体对ATM抑制剂表现出最大的细胞毒性。此外,ATM抑制剂使XRCC8突变体对离子辐射敏感,然而,XRCC8突变株V-G8表达的ATM蛋白水平降低。负责XRCC8表型的基因可能不是ATM,但与ATM功能高度相关。这些结果表明,XRCC8突变是PARP抑制剂通过破坏细胞周期调节以HR修复无关的方式诱导合成致死性的靶标。我们的发现扩大了PARP抑制剂在缺乏HR修复以外的DNA损伤反应基因的肿瘤中的潜在应用,XRCC8的进一步研究可能有助于这项研究。
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XRCC8 mutation causes hypersensitivity to PARP inhibition without Homologous recombination repair deficiency

PARP inhibitors inflict severe toxicity to homologous recombination (HR) repair deficient cells because DNA damages induced by PARP inhibition result in lethal DNA double strand breaks in the absence of HR repair during DNA replication. PARP inhibitors are the first clinically approved drugs designed for synthetic lethality. The synthetic lethal interaction of PARP inhibitors is not limited to HR repair deficient cells. We investigated radiosensitive mutants isolated from Chinese hamster lung origin V79 cells to identify novel synthetic lethal targets in the context of PARP inhibition. HR repair deficient BRCA2 mutant cells were used for positive control. Among tested cells, XRCC8 mutants presented hypersensitivity to PARP inhibitor, Olaparib. XRCC8 mutants showed elevated sensitivity to bleomycin and camptothecin similar to BRCA2 mutants. XRCC8 mutants presented an elevation of γ-H2AX foci formation frequency and S-phase dependent chromosome aberrations with Olaparib treatment. Enumerated damage foci following Olaparib treatment were observed to be elevated in XRCC8 as in BRCA2 mutants. Although this may suggest that XRCC8 plays a role in a similar DNA repair pathway as BRCA2 in HR repair, XRCC8 mutants presented functional HR repair including proper Rad51 foci formation and even elevated sister chromatid exchange frequencies with PARP inhibitor treatment. For comparison, RAD51 foci formation was suppressed in HR repair deficient BRCA2 mutants. Additionally, XRCC8 mutants did not display delayed mitotic entry with PARP inhibitors whereas BRCA2 mutants did. XRCC8 mutant cell line has previously been reported as possessing a mutation in the ATM gene. XRCC8 mutants displayed maximum cytotoxicity to ATM inhibitor among tested mutants and wild type cells. Furthermore, the ATM inhibitor sensitized XRCC8 mutant to ionzing radiation, however, XRCC8 mutant V-G8 expressed reduced levels of ATM protein. The gene responsible for XRCC8 phenotype may not be ATM but highly associated with ATM functions. These results suggest that XRCC8 mutation is a target for PARP inhibitor-induced synthetic lethality in HR repair independent manner via the disruption of cell cycle regulation. Our findings expand the potential application of PARP inhibitors in tumors lacking DNA damage responding genes other than HR repair, and further investigation of XRCC8 may contribute to this research.

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来源期刊
CiteScore
4.90
自引率
0.00%
发文量
24
审稿时长
51 days
期刊介绍: Mutation Research (MR) provides a platform for publishing all aspects of DNA mutations and epimutations, from basic evolutionary aspects to translational applications in genetic and epigenetic diagnostics and therapy. Mutations are defined as all possible alterations in DNA sequence and sequence organization, from point mutations to genome structural variation, chromosomal aberrations and aneuploidy. Epimutations are defined as alterations in the epigenome, i.e., changes in DNA methylation, histone modification and small regulatory RNAs. MR publishes articles in the following areas: Of special interest are basic mechanisms through which DNA damage and mutations impact development and differentiation, stem cell biology and cell fate in general, including various forms of cell death and cellular senescence. The study of genome instability in human molecular epidemiology and in relation to complex phenotypes, such as human disease, is considered a growing area of importance. Mechanisms of (epi)mutation induction, for example, during DNA repair, replication or recombination; novel methods of (epi)mutation detection, with a focus on ultra-high-throughput sequencing. Landscape of somatic mutations and epimutations in cancer and aging. Role of de novo mutations in human disease and aging; mutations in population genomics. Interactions between mutations and epimutations. The role of epimutations in chromatin structure and function. Mitochondrial DNA mutations and their consequences in terms of human disease and aging. Novel ways to generate mutations and epimutations in cell lines and animal models.
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