Investigating the function of MTBP in lymphoma

研究 MTBP 在淋巴瘤中的功能

• 批准号: 8780334
• 负责人: Matthew Vincent Puccetti
• 金额: $ 2.73万
• 依托单位: VANDERBILT UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2015
• 资助国家: 美国
• 起止时间: 2015-03-01 至 2019-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8780334
• 关键词: B-Cell Lymphomas; BHLH Protein; Binding; Binding Proteins; Biochemical; Biological Models; Burkitt Lymphoma; Cell Cycle Progression; Cell Line; Cell Proliferation; Cessation of life; Complex; Data; Development; Diagnosis; Disease; Doctor of Philosophy; Education; Gene Targeting; Genes; Genetic; Genetic Transcription; Goals; Growth; Hematopoietic Neoplasms; Human; Individual; Journals; Knockout Mice; Knowledge; Laboratories; Learning; Link; Literature; Lymphoma; Lymphomagenesis; Maintenance; Malignant Neoplasms; Mass Spectrum Analysis; Mediating; Mentors; Molecular; Mus; Non-Hodgkin' s Lymphoma; Oncogenes; Oncogenic; Patients; Physicians; Process; Protein Binding; Protein Overexpression; Proteins; Regulation; Reporting; Research; Role; Scientist; Signal Transduction; Students; Testing; Therapeutic; Therapeutic Intervention; Training; United States; Universities; Up-Regulation; Yeasts; anticancer research; c-myc Genes; cancer cell; career development; cell growth; chromatin modification; clinically relevant; clinically significant; cofactor; design; human disease; improved; in vitro Model; in vivo; insight; knowledge base; medical schools; meetings; mouse model; novel; overexpression; programs; promoter; protein expression; protein function; public health relevance; research study; therapeutic target; transcription factor; tumor; yeast two hybrid system

DESCRIPTION (provided by applicant): Cancer cells rely on oncogene-induced, hyper-proliferative signaling for growth and survival. c-Myc, a transcription factor which regulates cell cycle progression, cell growth and proliferation, is one of the most commonly overexpressed oncogenes in human cancer. Myc is overexpressed in 70% of human malignancies, including non-Hodgkin lymphoma, a cause of approximately 20,000 deaths in the United States each year. Despite decades of research into the functions and activity of Myc, much remains unresolved and there have been no successful therapies that target Myc to date. Recently, it has been proposed that targeting Myc indirectly may help overcome the lack of successful therapies for treating Myc-driven cancers. However, Myc regulation is highly complex and the identity and function of many of the proteins that regulate Myc activity remain unknown or poorly characterized. Thus, it is of critical importance to identify and evaluate proteins that interact wth Myc and regulate its function. We have preliminary data suggesting MTBP, a protein which we have previously shown to be linked to Myc-driven proliferation and lymphomagenesis, associates in a complex with Myc and regulates its oncogenic functions. Therefore, we hypothesize MTBP is a novel transcriptional regulator of Myc and has a critical role in lymphoma development and survival. To test this hypothesis, we propose two specific aims that utilize both in-vivo and in-vitro model systems. In the Aim 1, we will utilize molecular and biochemical strategies to elucidate the mechanism by which MTBP regulates Myc transcriptional activity. In Aim 2, we will employ in-vivo mouse model systems to evaluate the oncogenic activity of MTBP and characterize its role in lymphoma development and survival. We will also utilize human lymphoma cell lines to correlate our findings with mice to humans and to provide clinical relevance. Our results will significantly enhance our understanding of how Myc is regulated and will characterize the functions of a novel protein that regulates Myc. We anticipate that our findings will identify a novel target for treating Myc- driven malignancies. The challenging, comprehensive training that students in the MD/PhD program at the Vanderbilt University School of Medicine undergo will allow me to fulfill the goals of this proposal and will provide me with the education necessary to be a successful, independent physician-scientist. Throughout my training, I will learn to think critically, evaluate data, develop novel hypotheses and successfully answer scientific questions in the laboratory. This will be accomplished through seminars, journal clubs, didactic coursework, scientific meetings, analysis of the literature and thoughtful discussions with my mentor, thesis committee and other scientists. The educational and career development objectives outlined in this proposal will help me fulfill my goal of becoming a successful, independent physician-scientist in cancer research.

描述（由申请人提供）：癌细胞依赖于癌基因诱导的超增殖信号来生长和存活。c-Myc，一种调节细胞的转录因子