Mechanisms of transcriptional repression by p53 during hypoxic stress

缺氧应激期间 p53 转录抑制的机制

• 批准号: 7276847
• 负责人: ADAM J KRIEG
• 金额: $ 5.29万
• 依托单位: STANFORD UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-12-01 至 2010-11-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7276847
• 关键词: Apoptosis; Binding; Biochemical; Cancerous; Cell Hypoxia; Cells; Cellular Stress; Cultured Cells; DNA Damage; Event; Future; Gene Expression; Gene Expression Regulation; Gene Targeting; Genes; Goals; Hypoxia; Lead; Mediating; Microarray Analysis; Modeling; Mus; Mutate; Mutation; Numbers; Oxygen; Pathway interactions; Protein p53; Repression; Series; Stress; TP53 gene; Testing; Transactivation; Transcriptional Activation; Transcriptional Regulation; Tumor Suppressor Genes; Wound Healing; angiogenesis; cancer therapy; chromatin immunoprecipitation; gene repression; member; neoplastic cell; promoter; research study; response; transcription factor; tumor; tumor growth; tumor progression; tumorigenesis

DESCRIPTION (provided by applicant): Cellular hypoxia is a physiologically relevant cellular stress that triggers a host of cellular responses involved in tissue repair, angiogenesis, and tumorigenesis. A major cellular component of this phenomena is the tumor suppressor p53, which is stabilized by hypoxic stress. In contrast to transactivation phenomena observed during DNA damaging stress, hypoxia appears to have a distinctly different mechanism of transcriptional regulation, even though many of the downstream cellular effects are similar. This implies that p53 can mediate a number of its tumor suppressive functions through several non-intersecting pathways. The objective of this proposal is to determine how p53 suppresses tumor progression during hypoxic stress. To achieve this goal we will use a series of hypoxia regulated p53 constructs to identify genes that are specifically downregulated during hypoxia. We will use a combination of expression microarray technology and chromatin immunoprecipitation to identify direct targets of p53 repression in a cell culture model. Complementary mouse tumor studies will be used to verify the importance of general and specific gene repression on tumor cell apoptosis in the hypoxic regions of tumors. These studies will be essential for future experiments defining the functional consequences of transcriptional repression by p53. The low oxygen concentrations (hypoxia) that occur in tumors often lead to the formation of more aggressive tumors. The tumor suppressor gene p53 is frequently mutated in hypoxic tumors, aiding in the progression of tumor growth. Understanding how p53 regulates gene expression in hypoxic tumors will lead to the identification of new pathways to target for cancer therapies.

描述（由申请人提供）：细胞缺氧是一种生理学相关的细胞应激，可触发参与组织修复、血管生成和肿瘤发生的大量细胞反应。这种现象的一个主要细胞成分是肿瘤抑制因子p53，它通过缺氧应激而稳定。与DNA损伤应激过程中观察到的反式激活现象相反，缺氧似乎具有明显不同的转录调控机制，尽管许多下游细胞效应是相似的。这意味着p53可以通过几个非交叉途径介导其肿瘤抑制功能。这个建议的目的是确定p53如何在缺氧应激期间抑制肿瘤进展。为了实现这一目标，我们将使用一系列缺氧调节的p53构建体来鉴定在缺氧期间特异性下调的基因。我们将使用表达微阵列技术和染色质免疫沉淀相结合，以确定在细胞培养模型中的p53抑制的直接目标。互补的小鼠肿瘤研究将被用来验证一般和特定的基因抑制肿瘤细胞凋亡的重要性，在肿瘤的缺氧区域。这些研究将是必不可少的，为未来的实验定义转录抑制p53的功能后果。肿瘤中出现的低氧浓度（缺氧）通常会导致更具侵袭性的肿瘤的形成。肿瘤抑制基因p53在缺氧肿瘤中经常发生突变，有助于肿瘤生长的进展。了解p53如何调节缺氧肿瘤中的基因表达将有助于确定癌症治疗的新途径。