Imapct of Renox on HIF-alpha in Renal Cancer

Renox 对肾癌 HIF-α 的影响

• 批准号: 6899282
• 负责人: JODI Kathleen MARANCHIE
• 金额: $ 12.91万
• 依托单位: UNIV OF MASSACHUSETTS MED SCH WORCESTER
• 依托单位国家: 美国
• 财政年份: 2003
• 资助国家: 美国
• 起止时间: 2003-08-15 至 2006-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6899282
• 关键词: NAD(P)H dehydrogenase; aerobiosis; angiogenesis; biological signal transduction; enzyme activity; free radical oxygen; hypoxia inducible factor 1; kidney cell; kidney neoplasms; laboratory mouse; oxidative stress; posttranslational modifications; protein structure function; tissue /cell culture; tumor suppressor genes

DESCRIPTION (provided by applicant): Renal cell carcinoma (RCC) takes 12,000 American lives each year. Existing systemic therapies are curative in fewer than 10% of patients, and targeted therapeutic approaches are needed. Loss of the von Hippel Lindau (VHL) tumor suppressor is an early event in the development of most clear cell RCC, and preliminary studies have indicated that a critical function of VHL is ubiquitin-mediated degradation of hypoxia inducible factor alpha (HIF-alpha). HIF-alpha stability and transactivation are regulated by hypoxia and redox signaling by two independent mechanisms that involve binding of VHL and the transcriptional co-activator CBP/p300. A novel kidney-specific, superoxide-producing NAD(P)H oxidase, Renox, was recently described and implicated in oxygen sensing for maintenance of oxygen homeostasis via secretion of erythropoeitin. This exclusive renal function is known to require HIF transcriptional activation. The hypothesis of this proposal is that Renox-mediated accumulation of reactive oxygen species (ROS) within the renal cell influences activation of HIF-( leading to malignant transformation in the absence of functional VHL. There are three major aims of this work. The first is to determine the effect of Renox and ROS upon HIF-alpha regulation and activity. A second aim is to determine the effect of redox signaling upon HIF-alpha post-translational modification. The final aim is to specifically inhibit Renox function to determine its effects on the tumorigenic phenotype of renal cell carcinoma. Although this work is of high relevance to renal carcinogenesis, its has broader implications in the areas of renal microenvironment, oxidative stress in disease states, and general renal physiology. The candidate is a urologist with expertise in the area of molecular genetics of kidney cancer. She recently completed a research fellowship in urologic oncology at the National Cancer Institute. The candidate seeks to establish a career as an independent physician-scientist in an academic setting where 75% of her time is devoted to the laboratory and 25% to teaching and.clinical work. This will be achieved by a comprehensive program to acquire both technical and intellectual skills under the guidance of two distinguished and outstanding mentors, Shuk Mei Ho and Gary Stein, and to draw upon the scientific strengths of a number of investigators within the UMass Medical School community. This will provide an excellent environment for completion of this project and a basis for transition to independent investigator.

描述（由申请人提供）： 肾细胞癌（RCC）每年夺走12，000名美国人的生命。现有的系统性治疗在不到10%的患者中是治愈性的，并且需要靶向治疗方法。von Hippel Lindau（VHL）肿瘤抑制因子的缺失是大多数透明细胞RCC发展的早期事件，初步研究表明VHL的关键功能是泛素介导的缺氧诱导因子α（HIF-α）降解。HIF-α的稳定性和反式激活受缺氧和氧化还原信号传导的调节，这两种独立的机制涉及VHL和转录共激活因子CBP/p300的结合。Renox是一种新的肾脏特异性的产生超氧化物的NAD（P）H氧化酶，最近被描述并参与氧传感，通过分泌促红细胞生成素维持氧稳态。已知这种排他的肾功能需要HIF转录激活。该建议的假设是肾细胞内Renox介导的活性氧（ROS）的积累影响HIF-α的活化，导致在功能性VHL不存在的情况下的恶性转化。这项工作有三个主要目标。第一个是确定Renox和ROS对HIF-α调节和活性的影响。第二个目的是确定氧化还原信号传导对HIF-α翻译后修饰的影响。最终目的是特异性抑制Renox功能，以确定其对肾细胞癌致瘤表型的影响。虽然这项工作是高度相关的肾癌发生，其在肾脏微环境，疾病状态下的氧化应激，和一般的肾脏生理学领域有更广泛的影响。候选人是一名泌尿科医生，具有肾癌分子遗传学领域的专业知识。她最近在国家癌症研究所完成了泌尿肿瘤学的研究奖学金。候选人寻求在学术环境中作为独立的医生-科学家建立职业生涯，其中75%的时间用于实验室，25%用于教学和临床工作。这将通过一个全面的计划来实现，在两位杰出的导师Shuk Mei Ho和加里Stein的指导下获得技术和智力技能，并利用麻省大学医学院社区内一些研究人员的科学优势。这将为完成该项目提供一个良好的环境，并为过渡到独立调查员奠定基础。