Cooperating genes in inv (16) acute myeloid leukemia

inv (16) 急性髓系白血病的协同基因

• 批准号: 7260867
• 负责人: LUCIO H. CASTILLA
• 金额: $ 35.14万
• 依托单位: UNIV OF MASSACHUSETTS MED SCH WORCESTER
• 依托单位国家: 美国
• 财政年份: 2002
• 资助国家: 美国
• 起止时间: 2002-08-01 至 2012-01-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7260867
• 关键词: Acute Myelocytic Leukemia; Affect; Biochemical; Biological Assay; Cell Differentiation process; Chromosomal translocation; Chromosomes, Human, Pair 16; Clonal Expansion; Code; Core-Binding Factor; Development; Funding; Genes; Genetic; Goals; Growth; Hematopoiesis; Hematopoietic; Hematopoietic stem cells; Human; In Vitro; Insertional Mutagenesis; Knock-in Mouse; Leukemic Cell; MYH11 gene; Maintenance; Malignant Neoplasms; Mediating; MicroRNAs; Modeling; Molecular; Mus; Mutation; Myelogenous; Myeloid Leukemia; Myosin Heavy Chains; Oncogenes; Oncogenic; Pathway interactions; Play; Process; Protein Overexpression; Research Personnel; Role; Signal Transduction; Testing; Transforming Growth Factor beta; Transplantation; base; cancer cell; design; fusion gene; human CBFB protein; human MYH11 protein; improved; in vivo; leukemia; mouse model; progenitor; programs; research study; self-renewal; transcription factor

DESCRIPTION (provided by applicant): The CBFB-MYH11 fusion oncogene is frequently found in acute myeloid leukemia (AML). Our long term goal is to elucidate the molecular mechanisms that determine CBFB-MYH11-mediated leukemia progression in order to provide targets for the design of improved therapies. Our general hypothesis is that CBFB-MYH11 expression reduces hematopoietic stem cell differentiation and proliferation, and that cooperating mutations affect programs associated with proliferation, and survival. We have determined that Cbfb-MYH11 induces AML in cooperation with other mutations. We have created a conditional mouse model to show that expression of the fusion gene reduced the differentiation and proliferation ability of hematopoietic progenitors and created leukemia precursors in the myeloid compartment. Furthermore, we have identified cooperating genes, such as the transcription factors Plag1 and PlagL2 and the microRNA cluster miR17-92, and shown that constitutive expression of the transcription factor PlagL2 expanded myeloid progenitors and induced AML in the presence of Cbfb-MYH11. Based on these findings, the specific aims of this proposal are to: (1) determine PlagL2 role in proliferation and self-renewal of hematopoietic progenitors. We will use competitive repopulation and serial transplantation assays to assess the effect of (a) PlagL2-loss, and (b) constitutive PlagL2 expression, in long term-hematopoietic stem cells. (2) define the mechanism of PlagL2 function in leukemia progression. Preliminary experiments indicated that PlagL2 induces Mpl/Jak2 and TGF-beta signaling. We will combine in vivo and biochemical assays to determine the molecular mechanism of PlagL2 function in the (a) Mpl/Jak2 and (b) TGF-beta pathways. In addition, we will test whether Plag expression is necessary for maintenance of leukemia. (3) determine the role of micro-RNAs in CBF-SMMHC -mediated acute myeloid leukemia. Preliminary genetic evidence indicated that micro-RNAs can cooperate with Cbfb-MYH11 in leukemia progression. We will use in vivo assays to identify the mechanism of microRNA transformation.

描述（由申请人提供）：CBFB-MYH 11融合癌基因常见于急性髓性白血病（AML）。我们的长期目标是阐明决定CBFB-MYH 11介导的白血病进展的分子机制，以便为设计改进的疗法提供靶点。我们的一般假设是CBFB-MYH 11表达降低造血干细胞分化和增殖，并且协同突变影响与增殖和存活相关的程序。我们已经确定Cbfb-MYH 11与其他突变协同诱导AML。我们已经建立了一个条件性小鼠模型，以显示融合基因的表达降低了造血祖细胞的分化和增殖能力，并在骨髓室中产生了白血病前体。此外，我们已经确定了合作基因，如转录因子Plag 1和PlagL 2和microRNA簇miR 17 -92，并表明转录因子PlagL 2的组成型表达在Cbfb-MYH 11的存在下扩增骨髓祖细胞并诱导AML。基于这些发现，本建议的具体目的是：（1）确定PlagL 2在造血祖细胞增殖和自我更新中的作用。我们将使用竞争性再增殖和系列移植测定来评估（a）PlagL 2损失和（B）组成性PlagL 2表达在长期造血干细胞中的作用。(2)明确PlagL 2在白血病进展中的作用机制。初步实验表明，PlagL 2诱导Mpl/Jak 2和TGF-β信号传导。我们将结合联合收割机体内和生物化学测定来确定PlagL 2在（a）Mpl/Jak 2和（B）TGF-β途径中功能的分子机制。此外，我们将测试Plag表达是否是维持白血病所必需的。(3)确定微小RNA在CBF-SMMHC介导的急性髓系白血病中的作用。初步的遗传学证据表明，micro-RNA可以与Cbfb-MYH 11在白血病进展中协同作用。我们将使用体内测定来鉴定microRNA转化的机制。