Targeting invasion and DNA DSB repair in glioma with a multi-pronged approach.

多管齐下，针对神经胶质瘤的侵袭和 DNA DSB 修复。

• 批准号: 8206662
• 负责人: KRISTOFFER Carl VALERIE
• 金额: $ 19.51万
• 依托单位: VIRGINIA COMMONWEALTH UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-12-15 至 2013-11-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8206662
• 关键词: Adjuvant; Animal Model; Animals; Ataxia-Telangiectasia-Mutated protein kinase; BRCA1 gene; BRCA2 gene; Bioluminescence; Brain; Brain Neoplasms; Brain Stem; Cannulas; Cell Cycle; Cell Death; Cells; Chemosensitization; Clinical Trials; Coculture Techniques; Convection; DNA Double Strand Break; DNA Repair; DNA biosynthesis; Data; Development; Diagnosis; Disease; Double Strand Break Repair; Drug Combinations; Funding; Future; Glioblastoma; Glioma; Goals; Human; Human Engineering; In Vitro; Inflammation; Late Effects; Lead; Letters; Life Expectancy; Low Dose Radiation; Malignant Neoplasms; Malignant neoplasm of brain; Modeling; Molecular; Mus; Mutation; Normal Cell; PTEN gene; Pathway interactions; Patients; Pharmaceutical Preparations; Pharmacologic Substance; Phase; Poly(ADP-ribose) Polymerases; Population; Preclinical Testing; Procedures; Process; Proliferating; Proteins; Proto-Oncogene Proteins c-akt; Publishing; Pump; Radiation; Radiation therapy; Radiation-Sensitizing Agents; Radio; Radiosensitization; Reagent; Reporting; Role; S Phase; Safety; Signal Transduction; Site; Specificity; Staging; Stem cells; Technology; Testing; Therapeutic; Therapeutic Effect; Therapeutic Intervention; Toxic effect; Transgenic Mice; Translating; Treatment Efficacy; Xenograft Model; Xenograft procedure; animal efficacy; base; cell injury; cell motility; clinical practice; combat; fluorescence imaging; glioma cell line; homologous recombination; improved; in vivo; inhibitor/antagonist; insight; killings; kinase inhibitor; migration; neoplastic cell; nerve stem cell; nestin protein; neurogenesis; novel; novel therapeutic intervention; outcome forecast; pre-clinical; progenitor; promoter; public health relevance; recombinational repair; repaired; research clinical testing; response; standard care; treatment strategy; tumor; tumor growth

DESCRIPTION (provided by applicant): We recently showed that the ATM inhibitor (ATMi), KU-60019, is a potent radiosensitizer, the first report published on this novel compound. Briefly, KU-60019 is a very specific ATM kinase inhibitor and superior over its predecessor KU-55933 and shows at least 10-fold better efficacy in vitro for radio sensitizing human glioma cells. In addition, pro-survival signaling through the AKT and ERK pathways is also inhibited by KU-60019. The ATMi does so irrespective of PTEN and p53 status. Our studies also showed that glioma cells migration and invasion in vitro were inhibited to a large extent perhaps by interfering with AKT and ERK signaling in the presence of ATMi. Thus, the potential benefit of KU-60019 as a radiosensitizer for GBM is not limited to its ability to block the DDR and potently radiosensitize glioma cells but also having the ability to inhibit invasion and spread of the cancer. Preclinical testing of KU-60019 as a radiosensitizer for glioma is ongoing. We would now like to determine whether the PARP inhibitor (PARPi) AZD2281/KU-59436 alone, in combination with KU-60019 and/or radiation would show improved therapeutic efficacy in a preclinical glioma model. AZD2281 targets and kills tumor cells with mutations in BRCA1/BRCA2, or cells that are defective in homologous recombination repair (HRR) failing to repair DNA double-strand breaks (DSBs) during replication. Thus, synergistic killing should occur in glioma cells treated with AZD2281 and KU-60019 during DNA synthesis even in the absence of radiation. Low dose radiation (d 2 Gy) is expected to enhance the toxicity to AZD2281 and KU-60019 and further increase killing and promote radiosensitization of cells in S-phase, the most radioresistant cell cycle phase. In fact, our preliminary data show that this multi-pronged approach kills human glioma cells with little to no toxicity to normal cells in co-cultures. Thus, proof-of-principle testing of this strategy in an animal glioma model is warranted. Except for stem cells and neural progenitors (NPs), the brain consists mostly of terminally differentiated cells that do not proliferate. Thus, aggressively growing glial brain tumors residing in the brain parenchyma would be very favorable for therapeutic intervention with AZD2281 in combination with the ATMi with radiation perhaps providing further potentiation. However, it is very important to examine what impact this treatment might have on the NPs so that appropriate steps can be taken to spare normal brain. Little is known about the molecular processes occurring in normal brain in response to radiation but in general it is believed that radiation of neural stem cell compartments results in impaired neurogenesis due to radiation late effects and inflammation. We hope that insights gained from the proposed animal studies will demonstrate proof-of-principle of a novel drug combination strategy for the treatment of GBM that would be effective and safe and with the full support of KuDOS Pharmaceuticals/AstraZeneca can relatively quickly be translated into a clinical trial. PUBLIC HEALTH RELEVANCE: At best, standard treatment of glioblastoma multiforme (GBM) prolongs patient survival by a little more than a year. Thus, there is great need for developing and testing novel therapeutic approaches to combat this dreadful disease. We have developed a multi-pronged strategy targeting invasion, pro-survival signaling as well as DNA repair for treating GBM and now propose to test this approach for proof-of-principle in an animal model.

描述（由申请人提供）：我们最近发现ATM抑制剂（ATMi）KU-60019是一种有效的放射增敏剂，这是关于这种新型化合物的首次报道。简而言之，KU-60019是一种非常特异的ATM激酶抑制剂，上级其前身KU-55933，并在体外显示出至少10倍的放射增敏人神经胶质瘤细胞的功效。此外，通过AKT和ERK途径的促存活信号传导也被KU-60019抑制。ATMi这样做与PTEN和p53状态无关。我们的研究还表明，ATMi的存在下，胶质瘤细胞的迁移和侵袭在很大程度上受到抑制，这可能是通过干扰AKT和ERK信号转导。因此，KU-60019作为GBM的放射增敏剂的潜在益处不限于其阻断DDR和有效放射增敏神经胶质瘤细胞的能力，而且还具有抑制癌症侵袭和扩散的能力。KU-60019作为神经胶质瘤放射增敏剂的临床前试验正在进行中。 我们现在想要确定单独的PARP抑制剂（PARPi）AZD 2281/KU-59436与KU-60019和/或放射的组合是否会在临床前胶质瘤模型中显示改善的治疗功效。AZD 2281靶向并杀死BRCA 1/BRCA 2突变的肿瘤细胞，或同源重组修复（HRR）缺陷的细胞，无法修复复制过程中的DNA双链断裂（DSB）。因此，即使在没有辐射的情况下，在DNA合成期间用AZD 2281和KU-60019处理的胶质瘤细胞中也会发生协同杀伤。预计低剂量辐射（d 2戈伊）可增强对AZD 2281和KU-60019的毒性，并进一步增加杀伤作用，促进S期细胞（最具辐射抗性的细胞周期阶段）的辐射增敏作用。事实上，我们的初步数据表明，这种多管齐下的方法杀死了人类胶质瘤细胞，对共培养中的正常细胞几乎没有毒性。因此，在动物神经胶质瘤模型中验证该策略的原理是必要的。 除了干细胞和神经祖细胞（NP），大脑主要由不增殖的终末分化细胞组成。因此，存在于脑实质中的侵袭性生长的神经胶质脑肿瘤将非常有利于AZD 2281与ATMi组合的治疗干预，放射可能提供进一步的增强作用。然而，研究这种治疗可能对NP产生的影响是非常重要的，以便采取适当的措施来保护正常的大脑。对正常大脑中发生的对辐射的反应的分子过程知之甚少，但一般认为，神经干细胞隔室的辐射由于辐射迟发效应和炎症导致神经发生受损。 我们希望从拟议的动物研究中获得的见解将证明用于治疗GBM的新型药物组合策略的原理证明，该策略将是有效和安全的，并且在KuDOS Pharmaceuticals/AstraZeneca的全力支持下，可以相对快速地转化为临床试验。 公共卫生相关性：在最好的情况下，多形性胶质母细胞瘤（GBM）的标准治疗使患者生存期延长一年多一点。因此，非常需要开发和测试新的治疗方法来对抗这种可怕的疾病。我们已经开发了一种多管齐下的策略，靶向入侵，促生存信号传导以及DNA修复，用于治疗GBM，现在建议在动物模型中测试这种方法的原理证明。