A FUNCTIONAL STUDY OF UBIQUITIN C-TERMINAL HYDROLASE L1 EXPRESSION IN B-LYMPHOMA

B 淋巴瘤中泛素 C 末端水解酶 L1 表达的功能研究

• 批准号: 7773331
• 负责人: Julia Shackelford
• 金额: $ 7.4万
• 依托单位: UNIV OF NORTH CAROLINA CHAPEL HILL
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-05-01 至 2012-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7773331
• 关键词: Adhesions; Affect; Apoptosis; B-Cell Lymphomas; B-Lymphocytes; Binding; Cell Cycle Progression; Cell Line; Cell physiology; Cells; Complex; Data; Deubiquitinating Enzyme; Deubiquitination; Diagnostic; Goals; Growth; Hodgkin Disease; Human; Hydrolase; Immigration; Lymphoid; Lymphoma; Malignant Neoplasms; Microtubules; Oncogenic; Pathway interactions; Physiological; Process; Property; Proteasome Inhibitor; Regulation; Role; Signal Pathway; System; Therapeutic; Tubulin; Ubiquitin; Virus; base; cancer cell; cancer therapy; cell transformation; enzyme activity; inhibitor/antagonist; migration; multicatalytic endopeptidase complex; neoplastic cell; novel; outcome forecast; public health relevance; small molecule; tumorigenesis; tumorigenic; ubiquitin C-terminal hydrolase

DESCRIPTION (provided by applicant): Elevated expression of Ubiquitin C-terminal Hydrolase L1 (UCH L1) has been observed and associated with a poor prognosis in a number of human malignancies, including B-cell lymphomas. Although the involvement of this deubiquitinating enzyme in oncogenesis has thus been suggested, verification is largely lacking, and physiological functions and regulation of UCH L1 in cancer cells are still mainly unknown. While the role of the ubiquitin/ proteasome system in cell oncogenic transformation is well etablished, the impact of deubiquitinating enzymes (DUBs) in this process is largely unexplored. Our recent studies show that Epstein-Bar Virus-dependent transformation of B-cells induces expression of Ubiquitin C-terminal Hydrolase L1 (UCH L1) in normal B- lymphocytes, and its deubiqutinating activity is involved in activation of oncogenic pathways. We propose to investigate whether expression and enzymatic activity of UCH L1 affects basic cellular functions such as proliferation, survival and migration in B-lymphoma cell lines. Understanding of these functional inputs will identify UCH L1 as a new player in cell cycle progression and a potential target for a broadly based therapeutic approach. PUBLIC HEALTH RELEVANCE: Closely involved in regulation of numerous signaling pathways in tumor cells, the ubiquitin system in the last several years has become an attractive target for anti-cancer therapy. Although some proteasome inhibitors are useful in treatment of a variety of malignancies by inducing apoptosis in cancer cells, targeting of other steps of the ubiquitin system, such as specific DUBs, might produce more selective effects, since ubiquitinating and deubiquitinating complexes specifically bind to potential substrates. Our preliminary results indicate that a small-molecule inhibitor of UCH L1 enzymatic activity inhibits trans-endothelial migration of B-lymphoma cells and therefore might have a potential anti-invasive effect on lymphoid cancers. The goal of this proposal is to obtain experimental data on UCH L1 physiological functions in transformed cells and potentially to validate the deubiquitinating enzyme UCH L1 as a diagnostic marker and a novel target for anti-cancer therapy in specific malignancies such as non-Hodgkins and certain Hodgkins lymphomas.

描述（由申请人提供）：在包括b细胞淋巴瘤在内的许多人类恶性肿瘤中，已观察到泛素c端水解酶L1 （UCH L1）的表达升高，并与预后不良相关。尽管这种去泛素化酶在肿瘤发生中的作用已被提出，但在很大程度上缺乏验证，并且UCH L1在癌细胞中的生理功能和调控仍主要是未知的。