Significance of mutations in human NOTCH1 in T cell acute lymphoblastic leukemia

人NOTCH1突变在T细胞急性淋巴细胞白血病中的意义

• 批准号: 7431665
• 负责人: MARK Y CHIANG
• 金额: $ 13.33万
• 依托单位: UNIVERSITY OF PENNSYLVANIA
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-06-01 至 2011-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7431665
• 关键词: Acute T Cell Leukemia; Adult; Alleles; Animal Model; Biological Models; Bite; C-terminal; Cancer Biology; Cancer Etiology; Candidate Disease Gene; Cell Line; Cell Nucleus; Cell membrane; Cells; Cessation of life; Child; Chromosomal translocation; Class; Classification; Complex; Data; Data Set; Development; Dominant-Negative Mutation; Drosophila genus; Event; Family; Funding; Gene Targeting; Genetic; Goals; Hematopoietic; Hematopoietic stem cells; Heterodimerization; Histocompatibility Testing; Homologous Gene; Human; Lead; Leukemic Cell; Life; Ligands; Malignant Neoplasms; Measures; Mediating; Mentorship; Microarray Analysis; Modeling; Molecular; Mus; Mutate; Mutation; NOTCH1 gene; Oncogenes; Oncogenic; Pathogenesis; Patients; Pear; Phenotype; Physicians; Relative (related person); Research; Research Institute; Research Personnel; Role; Sampling; Scientist; Signal Pathway; Signal Transduction; TAL1 gene; TLX1 gene; Testing; Time; Training Programs; anticancer research; career; cell growth; experience; follow-up; gain of function mutation; improved; inhibitor/antagonist; leukemogenesis; malignant phenotype; mutant; neoplastic; notch protein; novel therapeutics; professor; progenitor; receptor; research study; skills; small molecule; synergism; transcription factor; tumorigenesis

DESCRIPTION (provided by applicant): A recent study found activating Notch1 mutations in 55% of human T-ALL patient samples. These newly discovered mutations are distributed among two hotspots -- the heterodimerization (HD) and PEST domains. However, the relative importance and consequence of each mutation remains unknown and unexplored. My preliminary research suggests that a single activating mutation in the HD hotspot cannot induce T-ALL in mice unless a second mutation occurs in the PEST hotspot in cis. I will follow up on these observations by determining whether all HD mutations require concurrent PEST mutations and by identifying cooperating oncogenes during the multi-step pathogenesis of T-ALL. In order to understand the molecular mechanism by which Notch initiates and sustains oncogenesis, I will characterize the effect of Notch inhibition on the proliferation, survival, and differentiation of leukemic cell lines and use this information to develop a systematic strategy for testing putative target genes generated from microarray data sets. Together these studies should not only lead to an improved understanding of T-ALL pathogenesis but will also identify novel therapeutic strategies for treatment. This proposal describes a 5 year training program to develop an academic career in cancer biology. The experiments described in the proposal will provide valuable experience in the use and manipulation of murine genetic model systems for the study of cancer under the mentorship of Dr. Warren Pear. Dr. Pear is an associate professor at the Abramson Family Cancer Research Institute with extensive experience in the manipulation and analysis of animal models of leukemogenesis. Ultimately, the time spent in the development of this project will establish a line of inquiry in the field of leukemogenesis and will provide the skills necessary to establish myself as a successful physician scientist and independent researcher. Acute T cell lymphoblastic leukemia remains a deadly cancer in children and adults which cannot be cured in more than one out of every three to four patients. A recent breakthrough study has identified Notch1 mutations in the majority of patients with this cancer. My research seeks to uncover the significance of these mutations and the cancer-causing molecular events in the cell that are triggered by this mutation, which may provide new opportunities for therapy.

描述（由申请人提供）：最近的一项研究发现，55%的人类T-ALL患者样本中存在激活Notch 1突变。这些新发现的突变分布在两个热点-异源二聚化（HD）和PEST结构域。然而，每个突变的相对重要性和后果仍然未知和未探索。我的初步研究表明，HD热点中的单个激活突变不能诱导小鼠中的T-ALL，除非PEST热点顺式发生第二次突变。我将通过确定是否所有HD突变都需要同时发生PEST突变，并通过确定T-ALL多步骤发病过程中的协同癌基因来跟踪这些观察结果。为了了解Notch启动和维持肿瘤发生的分子机制，我将描述Notch抑制对白血病细胞系增殖、存活和分化的影响，并利用这些信息开发一种系统的策略，用于测试从微阵列数据集产生的推定靶基因。总之，这些研究不仅可以提高对T-ALL发病机制的理解，而且还可以确定新的治疗策略。 该提案描述了一个为期5年的培训计划，以发展癌症生物学的学术生涯。该提案中描述的实验将在Warren Pear博士的指导下为癌症研究提供使用和操作小鼠遗传模型系统的宝贵经验。Pear博士是Abramson家庭癌症研究所的副教授，在白血病动物模型的操作和分析方面拥有丰富的经验。最终，在这个项目的发展所花费的时间将建立在白血病发生领域的调查线，并将提供必要的技能，建立自己作为一个成功的医生科学家和独立的研究人员。 急性T细胞淋巴细胞白血病仍然是儿童和成人的致命癌症，每三到四名患者中就有一名无法治愈。最近的一项突破性研究发现大多数这种癌症患者都存在Notch 1突变。我的研究旨在揭示这些突变的意义以及由这种突变引发的细胞中致癌分子事件，这可能为治疗提供新的机会。