Deregulation of Ras Signaling in MLL-Induced Leukemia

MLL 诱导的白血病中 Ras 信号传导的失调

• 批准号: 7267831
• 负责人: MICHAELA LIEDTKE
• 金额: $ 13.81万
• 依托单位: STANFORD UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-08-01 至 2011-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7267831
• 关键词: Accounting; Acute; Acute leukemia; Address; Animal Model; Binding Proteins; Biochemical; Biochemical Process; Biological Assay; Biological Models; Blood Cells; CD34 gene; Cell Nucleus; Chimeric Proteins; Co-Immunoprecipitations; Complex; Development; Disease remission; Dysmyelopoietic Syndromes; Ensure; Event; Gene Mutation; Gene Rearrangement; Genetic; Genetic Transcription; Hematopoiesis; Human; In Vitro; Infant; Inferior; Lead; Link; Lymphoid; MLL gene; MLLT4 gene; Mass Spectrum Analysis; Mediating; Mentors; Molecular; Molecular Abnormality; Mus; Mutation; Myelogenous; Oncogene Proteins; Oncogenic; Pathway interactions; Patients; Pharmaceutical Preparations; Physicians; Property; Proteins; Proto-Oncogenes; Ras Signaling Pathway; Recruitment Activity; Research Design; Research Personnel; Research Training; Role; Scientist; Signal Transduction; Stem cells; Testing; Thinking; Topoisomerase Inhibitors; Transactivation; Umbilical Cord Blood; Xenograft Model; Xenograft procedure; alpha-Thalassemia; histone methyltransferase; inhibitor/antagonist; leukemia; leukemogenesis; neoplastic; novel; outcome forecast; programs; protein purification; response

DESCRIPTION (provided by applicant): The objective of this 5-year proposal is to provide the applicant with an integrated research training and mentoring program that will ensure her successful development as an independent physician scientist. We propose to investigate the mechanisms and develop model systems of transformation by a subset of mixed lineage leukemia (MLL) oncoproteins that may share dual roles to simultaneously activate Ras signaling and MLL transcriptional pathways. The histone methyltransferase MLL is a transcriptional regulator essential for embryonal hematopoiesis, and is frequently fused to various partner proteins in infant and secondary leukemia. The transforming ability of MLL fusion proteins is thought to be caused by aberrant transcriptional effector properties conferred by the fusion partner, but the exact mechanisms are poorly understood. We have identified the Ras association 1 domain of the MLL fusion partner AF6 as critical for activation of the oncogenic properties of MLL linking MLL-induced leukemogenesis to Ras. Also, it was recently found that due to fusion with MLL, cytoplasmic EEN and its interaction partner EEN binding protein (EBP) are abducted to the nucleus. As a result EBP no longer exerts its inhibitory function on the Ras pathway. Similarly, fusion of RASGAP to MLL results in sequestration of RASGAP in the nucleus and interferes with its ability to inhibit Ras. We hypothesize that transformation by MLL-AF6, MLL-EEN and MLL-RASGAP is in part mediated by activation of Ras and that inhibition of the Ras pathway is a suitable treatment approach for leukemias induced by these MLL-fusion proteins. To test this hypothesis, we propose the following specific aims. 1. Investigate the molecular mechanisms by which fusion with AF6, RASGAP and EEN activate the oncogenic potential of MLL. 2. Assess potential deregulation of the Ras pathway by the respective MLL fusion protein and investigate the effect of Ras pathway inhibition on their transforming ability in vitro. 3a) Establish a murine xenograft of MLL-AF6, MLL-EEN and MLL-RASGAP-induced leukemia using human cord blood cells transduced with the respective MLL fusion protein. 3b) Assess the efficacy of Ras-pathway inhibitors in the xenograft model for treatment of leukemia induced by MLL-AF6, MLL-EEN and MLL-RASGAP. These studies will lead to a better understanding of the molecular mechanisms of leukemogenesis mediated by a subset of MLL fusion proteins and may facilitate the development and testing of novel targeted therapies.

描述（由申请人提供）：这个为期5年的计划的目标是为申请人提供一个综合的研究培训和指导计划，以确保她成功发展成为一名独立的内科科学家。我们建议研究混合谱系白血病（MLL）癌蛋白子集的转化机制并开发模型系统，这些癌蛋白可能具有双重作用，同时激活Ras信号传导和MLL转录途径。组蛋白甲基转移酶MLL是胚胎造血所必需的转录调节因子，在婴儿和继发性白血病中经常与各种伴侣蛋白融合。MLL融合蛋白的转化能力被认为是由融合伙伴赋予的异常转录效应特性引起的，但确切的机制尚不清楚。我们已经确定了MLL融合伙伴AF6的Ras关联1结构域是激活MLL致癌特性的关键，将MLL诱导的白血病发生与Ras联系起来。此外，最近发现由于与MLL的融合，细胞质EEN及其相互作用伙伴EEN结合蛋白（EBP）被绑架到细胞核中。结果EBP不再对Ras通路发挥抑制作用。同样，RASGAP与MLL的融合导致RASGAP在细胞核中被隔离，并干扰其抑制Ras的能力。我们假设MLL-AF6、MLL-EEN和MLL-RASGAP的转化部分是由Ras的激活介导的，抑制Ras途径是治疗这些mll -融合蛋白诱导的白血病的合适方法。为了验证这一假设，我们提出以下具体目标。1. 探讨与AF6、RASGAP和EEN融合激活MLL致癌潜能的分子机制。2. 评估各自的MLL融合蛋白对Ras通路的潜在调节作用，并研究Ras通路抑制对其体外转化能力的影响。3a)利用分别转染MLL融合蛋白的人脐带血细胞，建立MLL- af6、MLL- een和MLL- rasgap诱导的白血病小鼠异种移植物。3b)评估ras通路抑制剂在异种移植模型中治疗MLL-AF6、MLL-EEN和MLL-RASGAP诱导的白血病的疗效。这些研究将有助于更好地理解MLL融合蛋白亚群介导的白血病发生的分子机制，并可能促进新型靶向治疗的开发和测试。