Molecular Characterization of p53R2 in Cancer

癌症中 p53R2 的分子表征

• 批准号: 6602739
• 负责人: STUART J WONG
• 金额: $ 18.75万
• 依托单位: MEDICAL COLLEGE OF WISCONSIN
• 依托单位国家: 美国
• 财政年份: 2003
• 资助国家: 美国
• 起止时间: 2003-05-01 至 2005-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6602739
• 关键词: DNA damage; DNA repair; clinical research; genetic markers; genetic polymorphism; head /neck neoplasm; human tissue; laser capture microdissection; linkage disequilibriums; neoplasm /cancer radiation therapy; p53 gene /protein; polymerase chain reaction; radiation genetics; ribonucleotide reductase; single nucleotide polymorphism; squamous cell carcinoma; therapy adverse effect

DESCRIPTION (provided by applicant): Radiation therapy is a primary treatment modality for patients with locally advanced head and neck squamous cell cancer (HNSCC). The prognosis of these patients is generally poor and the frequency and severity of treatment related side effects from radiation are unacceptably high. Efforts to understand the genetic basis of tumor and normal tissue response to radiation-induced DNA damage may help develop new treatment strategies for HNSCC. Efforts are underway to discover candidate genes that predict tumor or normal tissue response to radiation. A recently identified gene, called p53R2, is transcriptionally dependent upon p53 and appears to play an important role in repair of radiation-induced DNA damage, p53R2 displays significant homology to the R2 subunit of ribonucleotide reductase (RR) - the enzyme that catalyzes the rate limiting step of DNA synthesis (conversion of ribonucleotide diphosphates to deoxyribonucleotide diphosphates). RR is required to supply nucleotide pools for DNA synthesis and for repair of DNA damage. New data suggests that it is p53R2, rather than the R2 subunit, that provides the RR activity for radiation-induced DNA repair. Inactivation of p53R2 is thought to enhance the vulnerability of cells to radiation-induced damage. We hypothesize that in HNSCC, polymorphisms of the p53R2 gene alter the functional capacity of cells to repair radiation-induced DNA damage, and that specific mutations or polymorphisms of the gene predict adverse clinical response of tumor and normal tissue to radiation. We will test this hypothesis by examining a tissue bank of stage III and IV HNSCC patients treated in Radiation Therapy Oncology Group (RTOG) Trial 90-03. Two specific aims will be examined: (1) To examine somatic mutations of the p53R2 gene as a prognostic tumor marker of radiation therapy in HNSCC. We will identify and characterize p53R2 polymorphisms in tumor cells, and test the hypothesis that somatic mutations of the p53R2 gene confer adverse clinical outcome, and (2) To examine single nucleotide polymorphisms (SNPs) of the p53R2 gene as predictive markers of normal tissue response to radiation therapy in HNSCC. We will identify and characterize the frequency of p53R2 gene SNPs in HNSCC patients and test the hypothesis that p53R2 gene SNPs predict adverse normal tissue radiation effects in HNSCC patients treated with radiation.

描述（由申请方提供）：放射治疗是局部晚期头颈部鳞状细胞癌（HNSCC）患者的主要治疗方式。这些患者的预后通常较差，并且与放射治疗相关的副作用的频率和严重程度高得不可接受。努力了解肿瘤和正常组织对辐射诱导的DNA损伤的反应的遗传基础可能有助于开发HNSCC的新治疗策略。目前正在努力发现预测肿瘤或正常组织对辐射反应的候选基因。最近发现的一个基因，称为p53 R2，是转录依赖于p53，似乎在辐射诱导的DNA损伤的修复中发挥重要作用，p53 R2显示出显着的同源性，核糖核苷酸还原酶（RR）的R2亚基-催化DNA合成的限速步骤（核糖核苷酸二磷酸转化为脱氧核糖核苷酸二磷酸）的酶。需要RR来提供用于DNA合成和DNA损伤修复的核苷酸池。新的数据表明，是p53 R2，而不是R2亚基，为辐射诱导的细胞凋亡提供了RR活性。 DNA修复p53 R2的失活被认为增强了细胞对辐射诱导的损伤的脆弱性。我们假设在HNSCC中，p53 R2基因的多态性改变细胞修复辐射诱导的DNA损伤的功能能力，并且该基因的特定突变或多态性预测肿瘤和正常组织对辐射的不良临床反应。我们将通过检查放射治疗肿瘤组（RTOG）试验90-03中接受治疗的III期和IV期HNSCC患者的组织库来检验这一假设。本研究的目的有两个：（1）检测p53 R2基因的体细胞突变作为放射治疗的预后标志物。我们将鉴定和描述肿瘤细胞中p53 R2的多态性，并检验p53 R2基因的体细胞突变导致不良临床结果的假设;（2）检测p53 R2基因的单核苷酸多态性（SNP）作为HNSCC中正常组织对放射治疗反应的预测标志物。我们将确定和表征HNSCC患者中p53 R2基因SNP的频率，并检验p53 R2基因SNP预测接受放射治疗的HNSCC患者的不良正常组织放射效应的假设。