Post-Transcriptional Regulation in Colorectal Cancer

结直肠癌的转录后调控

• 批准号: 8616417
• 负责人: DAN ALAN DIXON
• 金额: $ 28.32万
• 依托单位: UNIVERSITY OF KANSAS MEDICAL CENTER
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-09-21 至 2014-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8616417
• 关键词: Post; Transcriptional; Regulation; Colorectal; Cancer

DESCRIPTION (provided by applicant): Colorectal cancer is a leading cause of cancer mortality among adults. Commonly observed in colon cancer cells and tumors is overexpression of many growth- and inflammation-associated immediate-early response genes. A critical point in controlling the expression of these factors in normal intestinal epithelium occurs through post-transcriptional mechanisms that regulate mRNA decay. The two primary RNA-binding proteins associated with post-transcriptional regulation are the mRNA stability factor Hu antigen R (HuR) and the mRNA decay factor tristetraprolin (TTP). Both of these factors bind AU-rich mRNA elements (ARE) present in a majority of cancer-associated immediate-early response gene transcripts and target the mRNA for stabilization or rapid decay. However, a characteristic feature observed in colon cancer cells and tumors is overexpression of the stability factor HuR and loss of expression of the decay factor TTP. These combined defects allow for stabilization and overexpression of cancer-associated growth factors. Based on these observations we hypothesize that loss of post-transcriptional regulation promotes intestinal epithelial cell tumorigenesis by selectively stabilizing AU-rich element containing-mRNA transcripts. The following specific aims are proposed to test this hypothesis. Specific Aim 1: Determine whether altered expression of the mRNA stability factor HuR and the mRNA decay factor TTP can promote intestinal cell transformation and tumorigenesis. Under Aim 1 we will determine whether HuR overexpression and TTP loss play a causal role in promoting epithelial cell transformation and tumorigenesis through a mechanism of defective rapid mRNA decay and cancer-associated gene overexpression. Specific Aim 2: Determine the ability of low-molecular- weight inhibitors of HuR and viral-mediated delivery of TTP to impact colon cancer cell growth and gene expression. The emphasis of this aim is to investigate the therapeutic potential of targeting HuR-mediated mRNA stabilization. Specific Aim 3: Determine if HuR overexpression and TTP loss in the murine gastrointestinal tract promotes cancer-associated gene expression and tumorigenesis in vivo. In this Specific Aim we will determine the in vivo significance of HuR overexpression and TTP loss in promoting intestinal tumorigenesis. Specific Aim 4: Determine the molecular events in colon cancer cells and tumors that promote HuR overexpression and silencing of TTP expression. Under this aim, we will determine the mechanisms promoting HuR expression and TTP gene silencing in colon cancer. This study will enhance our understanding of colorectal cancer biology and lead to the identification of novel molecular targets, which will improve current treatment and prevention strategies. PUBLIC HEALTH RELEVANCE: Colorectal cancers are a leading cause of cancer incidence and death among adult Americans. In colorectal cancer cells and tumors, uncontrolled expression of many growth- and inflammation-associated genes occurs. By better understanding the cellular mechanisms involved in controlling the expression of these factors, we aim to identify and define new molecular targets for controlling gene expression in colorectal cancer and improve current treatment and prevention strategies.

描述（由申请人提供）：结直肠癌是成人癌症死亡的主要原因。在结肠癌细胞和肿瘤中常见的是许多与生长和炎症相关的立即早期反应基因的过度表达。控制正常肠上皮中这些因子表达的关键点是通过调节 mRNA 衰减的转录后机制发生的。与转录后调节相关的两种主要 RNA 结合蛋白是 mRNA 稳定因子 Hu 抗原 R (HuR) 和 mRNA 衰减因子 tristetraprolin (TTP)。这两种因子都与大多数癌症相关的早期反应基因转录物中存在的富含 AU 的 mRNA 元件 (ARE) 结合，并以 mRNA 为目标进行稳定或快速衰减。然而，在结肠癌细胞和肿瘤中观察到的一个特征是稳定因子 HuR 的过度表达和衰变因子 TTP 的表达缺失。这些组合缺陷允许癌症相关生长因子的稳定和过度表达。基于这些观察，我们假设转录后调控的丧失通过选择性地稳定含有 mRNA 转录物的富含 AU 的元件来促进肠上皮细胞肿瘤的发生。提出以下具体目标来检验这一假设。具体目标 1：确定 mRNA 稳定因子 HuR 和 mRNA 衰减因子 TTP 表达的改变是否可以促进肠细胞转化和肿瘤发生。在目标 1 下，我们将确定 HuR 过度表达和 TTP 缺失是否通过有缺陷的快速 mRNA 衰减和癌症相关基因过度表达的机制在促进上皮细胞转化和肿瘤发生中发挥因果作用。具体目标 2：确定 HuR 的低分子量抑制剂和病毒介导的 TTP 递送影响结肠癌细胞生长和基因表达的能力。这一目标的重点是研究针对 HuR 介导的 mRNA 稳定化的治疗潜力。具体目标 3：确定小鼠胃肠道中 HuR 过度表达和 TTP 缺失是否会促进体内癌症相关基因表达和肿瘤发生。在这个具体目标中，我们将确定 HuR 过度表达和 TTP 丢失在促进肠道肿瘤发生中的体内意义。具体目标 4：确定结肠癌细胞和肿瘤中促进 HuR 过度表达和 TTP 表达沉默的分子事件。在此目标下，我们将确定结肠癌中促进HuR表达和TTP基因沉默的机制。这项研究将增强我们对结直肠癌生物学的理解，并确定新的分子靶点，从而改善当前的治疗和预防策略。 公共卫生相关性：结直肠癌是美国成年癌症发病率和死亡的主要原因。在结直肠癌细胞和肿瘤中，许多生长和炎症相关基因的表达不受控制。通过更好地了解控制这些因子表达的细胞机制，我们的目标是识别和定义控制结直肠癌基因表达的新分子靶点，并改进当前的治疗和预防策略。