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Use of CTEP portfolio compounds to counteract phenotype conversion in GBM

使用 CTEP 组合化合物来抵消 GBM 中的表型转换

基本信息

批准号：
10737830
负责人：
Frank Pajonk
金额：
$ 10.55万
依托单位：
UNIVERSITY OF CALIFORNIA LOS ANGELES
依托单位国家：
美国
项目类别：
财政年份：
2022
资助国家：
美国
起止时间：
2022-01-01 至 2026-12-31
项目状态：
未结题

来源：
https://reporter.nih.gov/project-details/10737830
关键词：
3-Dimensional Affect Basic Science Biological Assay Biological Markers Biology Cancer Therapy Evaluation Program Cell Differentiation process Cells Cholesterol Clinical Clinical Trials Clonal Evolution Combination Drug Therapy Combined Modality Therapy Data Disease Dose Drug Interactions Drug Kinetics Electromagnetic Energy Fatty Acids Gene Expression Profiling Generations Glioblastoma Glioma Goals Hypoxia In Vitro Level of Evidence Literature Malignant Neoplasms Malignant neoplasm of brain Metabolic Modality Modeling Nitric Oxide Pathway interactions Patient-Focused Outcomes Patients Pharmaceutical Preparations Phenotype Population Process Publishing Radiation Radiation Dose Unit Radiation Oncology Radiation therapy Recurrence Reporting Resources Scheme Specimen Surgical Oncology Testing Time Toxic effect Transgenic Mice Treatment Failure United States National Institutes of Health biomarker identification biomarker validation blood-brain barrier crossing cancer cell cancer stem cell chemotherapeutic agent cholesterol biosynthesis disorder control drug development effective therapy imaging system improved in vivo induced pluripotent stem cell inhibitor innovation malignant breast neoplasm mevalonate mouse model neoplastic cell nerve stem cell nestin protein neurogenesis novel patient derived xenograft model prevent radiation resistance radioresistant responders and non-responders self-renewal standard of care stem cells synergism targeted agent targeted treatment temozolomide therapy outcome therapy resistant tool trait tumor tumor initiation

项目摘要

SUMMARY/ABSTRACT Despite a tremendous effort in basic science, clinical trials, drug development, and technical advances in surgery and radiation oncology, glioblastoma remains incurable and improvements in overall survival have been marginal. While radiotherapy is still one of the most effective treatment options for glioblastoma, it cannot control the disease over time. This suggests that novel combination therapies are desperately needed to improve radiation treatment outcome for patients suffering from this disease. The studies outlined in this proposal are based on a hypothesis that is backed by our extensive preliminary data and rigorous published data in the literature. The overall hypothesis is that biomarker-based drug selection predicts synergistic lethality of combination therapies in GICs and glioblastoma bulk tumor cell populations, prevents radiation-induced GBM phenotype conversion and allows for individualized optimization of radiotherapy. The three aims of this study will address this aspect of glioma biology using an innovative tool to track GICs and their progeny, while leveraging the unique resources and expertise available at UCLA and the NIH/NCI CTEP portfolio of drugs. Aim 1 will identify compounds in the NCI CTEP portfolio that interfere with radiation-induced phenotype conversion in glioblastoma and develop biomarker profiles predictive of synergistic lethality in combination with radiation. Studies in Aim 2 will optimize combination therapies in vivo. Finally, Aim 3, will use patient avatar studies to validate biomarker-based drug selection in PDX models of glioblastoma.

摘要/摘要尽管在基础科学、临床试验、药物开发和技术进步方面做出了巨大努力手术和放射肿瘤学，胶质母细胞瘤仍然是不可治愈的，总体存活率的改善被边缘化了。虽然放射治疗仍然是胶质母细胞瘤最有效的治疗选择之一，但它不能随着时间的推移，控制疾病。这表明迫切需要新的联合疗法来治疗改善这种疾病患者的放射治疗结果。这篇文章中概述的研究建议是基于一个假设，该假设得到了我们广泛的初步数据和严格出版的支持文献中的数据。总体假设是，基于生物标记物的药物选择预测协同致命性。在GICs和胶质母细胞瘤肿瘤细胞群体中的联合治疗，防止辐射诱导 GBM表型转换，并允许个体化优化放射治疗。这样做的三个目的研究将使用一种跟踪GIC及其后代的创新工具来解决胶质瘤生物学的这一方面，同时利用加州大学洛杉矶分校和NIH/NCI CTEP药物组合的独特资源和专业知识。 AIM 1将鉴定NCI CTEP组合中干扰辐射诱导表型的化合物胶质母细胞瘤的转化和发展预测协同致死率的生物标志物辐射。AIM 2的研究将优化体内的联合治疗。最后，目标3，将使用患者头像在胶质母细胞瘤PDX模型中验证基于生物标记物的药物选择的研究。