Transcriptional Signatures of Homologous Recombination Deficiency for Targeted Ch

描述（由申请人提供）：DNA修复途径维持基因组的完整性，因此许多癌细胞在DNA修复的某些方面存在缺陷并不奇怪。幸运的是，这些癌症特异性DNA修复缺陷为肿瘤选择性治疗提供了新方法，如PARP1抑制剂对brca缺陷或同源重组（HR）缺陷肿瘤的合成致死率。因此，一个重要的目标和挑战是确定哪些肿瘤在DNA修复的各种特定途径中存在缺陷。据了解，DNA修复能力的变化将影响细胞功能在基线和响应基因毒性应激。此外，有人认为DNA修复能力的这些变化可能会重新编程细胞转录景观。最近的证据表明，这种重编程发生在多个层面，包括特定rna的合成和稳定性的变化，这表明DNA修复缺陷可能提供了独特的转录特征。我们期望与HR缺陷相关的RNA合成和稳定性特征将是独一无二的，并且可能有助于在不了解任何潜在基因缺陷的情况下识别HR缺陷。我们已经开发了一种全基因组方法来识别这种标记，称为“BrU-Seq”，其中新生rna的溴化吡呤脉冲标记与RNA-Seq相结合，以一种清晰和高效的方式揭示了对基因表达的大量影响，这是标准微阵列或RNA-Seq方法无法做到的。为了进一步了解正常细胞中突然（体细胞）DNA修复缺陷的影响，我们建议综合评估模型非致瘤性上皮细胞系MCF-10A中DNA修复基因在每个DNA修复途径中表达缺失后的所有编码和调控rna的动态状态。我们假设DNA修复缺陷会影响mRNA/microRNA的表达和稳定性，DNA修复途径特异性特征可用于预测对某些化疗药物的反应。具体来说，我们将使用BrU-Seq技术来(1)测量六种主要DNA修复途径中缺乏关键基因的等基因MCF-10A细胞系中所有编码和调控RNA物种的合成、稳定性和结构含量；(2)评估电离辐射和化疗药物替莫唑亚胺、顺铂和PARP抑制剂对相同细胞转录谱的基因毒性应激诱导的改变。这些研究将是鉴定肿瘤样本中与特定DNA修复途径缺陷相关的特征的关键的第一步，这些特征可能被用作生物标志物来预测对靶向化疗药物的反应。

DESCRIPTION (provided by applicant): DNA repair pathways maintain the integrity of the genome and it is therefore not surprising that many cancer cells are defective in some aspect of DNA repair. Fortunately, these cancer-specific DNA repair defects offer novel approaches for tumor-selective therapy such as the synthetic lethality of PARP1 inhibitors with BRCA-deficient or homologous recombination (HR)-deficient tumors. An important goal and challenge is thus to identify which tumors are defective in the various specific pathways of DNA repair. It is understood that changes in DNA repair capacity will impact cellular functions both at baseline and in response to genotoxic stress. Further, it has been suggested that these changes in DNA repair capacity may reprogram the cellular transcriptional landscape. Recent evidence suggests that this reprogramming occurs at multiple levels, including changes in the synthesis and stability of specific RNAs, suggesting that DNA repair deficiency may provide unique transcriptional signatures. It is our expectation that the RNA synthesis and stability signature associated with a defect in HR will be unique and may be useful in identifying HR defects without knowledge of any underlying gene defect. We have developed a genome-wide approach for identifying such a signature, termed "BrU-Seq", in which BromoUridine pulse-labeling of nascent RNAs is combined with RNA-Seq in a manner that reveals a remarkably large number of influences on gene expression with a clarity and efficiency not allowed by standard microarray or RNA-Seq approaches. To advance our understanding of the impact of a sudden (somatic) DNA repair defect in a normal cell, we propose to comprehensively evaluate the dynamic status of all coding and regulatory RNAs in the model non-tumorigenic epithelial cell line, MCF-10A, following loss of expression of DNA repair genes across each DNA repair pathway. We hypothesize that DNA repair defects will impact mRNA/microRNA expression and stability with DNA repair pathway-specific signatures that can be used to predict response to certain chemotherapeutic agents. Specifically, we will use BrU-Seq technology to (1) measure the synthesis, stability and structural content of all coding and regulatory RNA species in isogenic MCF-10A cell lines deficient in a key gene in each of the six major DNA repair pathways and (2) evaluate genotoxic stress-induced alterations in the transcriptional profile of the same cells in response to ionizing radiation and the chemotherapeutics temozolimide, cisplatin and PARP inhibitors. These studies will be a critical first step towards identifying signatures associated with specific DNA repair pathway defects in tumor samples that may be used as biomarkers to predict response to targeted chemotherapeutic agents.