The Role of t-Darpp in Esophageal Adenocarcinoma

t-Darpp 在食管腺癌中的作用

• 批准号: 7914391
• 负责人: WAEL EL-RIFAI
• 金额: $ 23.26万
• 依托单位: VANDERBILT UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-08-13 至 2012-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7914391
• 关键词: Adenocarcinoma; Adopted; Apoptosis; Apoptotic; Arts; Automobile Driving; Biological; Biological Process; Butyrates; Camptothecin; Cancer Etiology; Cancer cell line; Cell Death; Cell Survival; Cells; Ceramides; Cessation of life; Cloning; Complex; DARPP; Data; Diagnostic; Dopamine- and cAMP-regulated neuronal phosphoprotein; Doxycycline; Drug resistance; Esophageal; Esophageal Adenocarcinoma; Foundations; Gene Combinations; Gene Targeting; Gleevec; In Vitro; Incidence; Malignant Neoplasms; Malignant neoplasm of gastrointestinal tract; Mediating; Mitochondria; Molecular; Names; Normal tissue morphology; Oncogenes; PIK3CG gene; PTEN gene; Pathway interactions; Pharmaceutical Preparations; Phosphorylation; Phosphorylation Site; Population; Preventive; Protein Isoforms; Proteins; Proteomics; Proto-Oncogene Proteins c-akt; Relative (related person); Reporting; Roche brand of trastuzumab; Role; Signal Pathway; Signal Transduction; Stomach; Survival Rate; Testing; Therapeutic; Tumor Suppressor Genes; Tumor Suppressor Proteins; United States; Up-Regulation; Western World; addiction; base; cancer cell; carcinogenesis; functional outcomes; gastroesophageal junction adenocarcinoma; gastrointestinal; improved; in vivo; innovation; insight; mutant; new therapeutic target; novel; overexpression; public health relevance; research study; response; tumor; tumor growth

DESCRIPTION (provided by applicant): The incidence of upper gastrointestinal adenocarcinomas (UGCs; adenocarcinomas of the esophagus and stomach) has been rising steadily. Moreover, a sharp increase in the incidence of lower esophageal and gastroesophageal junction adenocarcinomas has been observed over the past three decades bearing the distinction of the fastest rising incidence of all cancers in the Western world. Overall relative 5-year survival rates are currently less than 20%. Improvement in our presently limited diagnostic, preventive, and therapeutic approach to UGCs is currently a pressing issue. This proposal is based on our original findings through the use of multiple molecular analyses in UGCs that led to the cloning and identification of t-DARPP as a novel cancer gene. We found over-expression of t-DARPP in approximately two-thirds of UGCs and analysis of its biological functions indicated that t-DARPP is a potent pro-survival protein. Using several drugs (camptothecin, butyrates, ceramides) we found that t-DARPP protects cancer cells against drug-induced cell death by a mechanism that includes activation of AKT survival pathway and up-regulation of BCL-2. We hypothesize that t-DARPP provides critical potent pro-survival and anti-apoptotic advantages to cancer cells leading to resistance to drug- induced cell death. We plan to investigate the molecular and biological roles of t-DARPP and determine the potential therapeutic value of its knockdown in UGCs. In Aim 1 of this proposal, we will investigate the molecular mechanism(s) by which t-DARPP phosphorylation sites regulate the AKT survival pathway. Based on our preliminary data, we will investigate the mechanisms by which t-DARPP regulates the PTEN tumor suppressor activity, localization, and stability in cancer cells. In Aim 2, we plan to investigate the effect of t- DARPP on drug resistance by testing its ability to abrogate drug-induced cell death. We will examine the role of t-DARPP in regulating the complex intrinsic apoptosis. Several recent reports suggest the oncogene addiction concept in cancer cells, where cancer cell survival becomes dependent on the expression of a critical survival protein. We will test the therapeutic potential of t-DARPP knockdown in vivo and whether its knockdown alone or in combination with the existing chemotherapeutics can boost the therapeutic response. In Aim 3, we will adopt powerful proteomic approaches for a systematic characterization of proteins that interact with t-DARPP and those that are downstream effectors in order to identify novel signaling pathways and biological functions that t-DARPP could mediate in cancer cells that remain unknown. In all our experiments, we will test its phosphorylation mutants in order to characterize the molecular and functional role(s) of each of these phosphorylation sites in cancer cells. We anticipate that completion of the suggested experiments will provide a significant insight into the role of t-DARPP, as a novel protein, in upper gastrointestinal adenocarcinomas. PUBLIC HEALTH RELEVANCE: This proposal connects in vitro and in vivo experiments in order to characterize the role(s) of t-DARPP in upper gastrointestinal carcinogenesis. We plan to investigate the role of t-DARPP in regulating the intrinsic apoptosis and evaluate its potential as a novel therapeutic target. State-of-the-art proteomic approaches will be employed to identify t-DARPP interacting proteins as well as its molecular signaling targets.

描述（由申请人提供）：上消化道腺癌（UGC;食管和胃的腺癌）的发病率一直在稳步上升。此外，在过去的三十年中，观察到食管下段和胃食管连接部腺癌的发病率急剧增加，这是西方世界所有癌症中发病率上升最快的。总体相对5年生存率目前低于20%。改善我们目前有限的诊断，预防和治疗方法UGC目前是一个紧迫的问题。该建议是基于我们通过在UGC中使用多重分子分析的原始发现，该发现导致了t-DARPP作为一种新的癌症基因的克隆和鉴定。我们发现t-DARPP在大约三分之二的UGC中过表达，并且对其生物学功能的分析表明t-DARPP是一种有效的促生存蛋白。使用几种药物（喜树碱、丁酸盐、神经酰胺），我们发现t-DARPP通过包括AKT存活途径的激活和BCL-2的上调的机制保护癌细胞免于药物诱导的细胞死亡。我们假设t-DARPP为癌细胞提供关键的有效促存活和抗凋亡优势，导致对药物诱导的细胞死亡的抗性。我们计划研究t-DARPP的分子和生物学作用，并确定其在UGC中敲低的潜在治疗价值。在本提案的目标1中，我们将研究t-DARPP磷酸化位点调节AKT存活途径的分子机制。基于我们的初步数据，我们将研究t-DARPP调节癌细胞中PTEN肿瘤抑制活性、定位和稳定性的机制。在目的2中，我们计划通过测试t-DARPP消除药物诱导的细胞死亡的能力来研究其对耐药性的影响。我们将研究t-DARPP在调节复杂的内在凋亡中的作用。最近的几份报告提出了癌细胞中的癌基因成瘾概念，其中癌细胞的存活依赖于一种关键存活蛋白的表达。我们将在体内测试t-DARPP敲低的治疗潜力，以及其单独敲低或与现有化疗药物组合是否可以增强治疗反应。在目标3中，我们将采用强大的蛋白质组学方法，系统地表征与t-DARPP相互作用的蛋白质和下游效应物，以确定t-DARPP在癌细胞中可能介导的新信号通路和生物学功能，这些功能仍然未知。在我们所有的实验中，我们将测试其磷酸化突变体，以表征癌细胞中每个磷酸化位点的分子和功能作用。我们预计，完成建议的实验将提供一个显着的洞察t-DARPP的作用，作为一种新的蛋白质，在上消化道腺癌。公共卫生相关性：该建议将体外和体内实验相结合，以表征t-DARPP在上消化道癌发生中的作用。我们计划研究t-DARPP在调节内源性凋亡中的作用，并评估其作为新的治疗靶点的潜力。国家的最先进的蛋白质组学方法将被用来确定t-DARPP相互作用的蛋白质，以及其分子信号转导的目标。