Biomarker for Hepatocellular Carcinoma

肝细胞癌的生物标志物

• 批准号: 7486299
• 负责人: Jack R Wands
• 金额: $ 23.78万
• 依托单位: RHODE ISLAND HOSPITAL
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-08-17 至 2012-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7486299
• 关键词: Antibodies; Binding; Biodistribution; Biological Assay; Biological Markers; Cell Surface Proteins; Cell surface; Chronic; Chronic Hepatitis C; Cirrhosis; Detection; Development; Diagnosis; Disease; Early Diagnosis; Enzymes; Epidemic; Genes; Health Professional; Hepatitis B; Hepatitis B Virus; Hepatitis C; Hepatitis C virus; Human; Immunoassay; Immunoglobulin G; Incidence; Insulin Resistance; Lead; Length; Life Expectancy; Liver; Liver diseases; Mixed Function Oxygenases; Modeling; Monoclonal Antibodies; Mus; N-terminal; Non-Insulin-Dependent Diabetes Mellitus; Obesity; Pathogenesis; Patients; Primary carcinoma of the liver cells; Proteins; Purpose; Reagent; Recombinant Proteins; Risk Factors; Role; Screening procedure; Serum; Standards of Weights and Measures; Techniques; Time; United States; anti-IgG; base; expression cloning; improved; nonalcoholic steatohepatitis; novel; outcome forecast; tumor

DESCRIPTION (provided by applicant): Human hepatocellular carcinoma (HCC) is one of the most serious complications of chronic liver disease and cirrhosis. Even more disturbing is the observation that the average life expectancy from the time of diagnosis is approximately eight to ten months. The incidence of HCC has begun to increase in the United States principally due to the contribution of chronic hepatitis C (HCV) infection. In addition, with the obesity epidemic including Type II diabetes and insulin resistance, the emergence of non-alcoholic steatohepatitis (NASH) has begun to assume a larger role in the pathogenesis of this devastating disease due to the development of cirrhosis, a risk factor for HCC. More recently, there is widespread concern among health care professionals regarding the increase in HCC and the lack of optimal screening techniques that lead to or contribute to early diagnosis and treatment in the hope of improving the prognosis of this almost uniformly fatal disease. Thus, the purpose of this proposal is to validate a new marker that may be useful in the early diagnosis of HCC. In this regard, we have identified by monoclonal antibody (mAb) binding and expression cloning, a cell surface protein marker that is enhanced in HCC tumors. The gene encoding for this protein has been cloned and molecularly identified as aspartyl (asparaginyl) (¿-hydroxylase (HAAH) which appears to be highly expressed in most (>90%) hepatitis B (HBV) and HCV related HCC. Furthermore, this protein appears to be present in serum of such patients. Thus, we have established immunoassays to detect C and N terminal fragments as well as full length HAAH in serum using recombinant proteins as standards. Because this enzyme is expressed on the cell surface, we have recently developed human scFv and IgG antibodies directed against the various region of the molecule. These reagents will be used in biodistribution studies to target tumors in murine models of human HCC. Evidence will be presented to support the hypothesis that HAAH gene is a novel biomarker for HCC since expression appears to be highly associated with the pathogenesis of the disease. We plan to do the following. Specific Aim 1. Validate HAAH as a biomarker for HCC. Specific Aim 2. Further characterize human scFv fragments and IgG anti-AAH antibodies. It is likely that these new mAb based assays will be useful for the early detection of HCC and human anti-HAAH antibodies may be employed as targeting reagents for the specific detection of HCC in the liver.

描述（申请人提供）：人肝细胞癌（HCC）是慢性肝病和肝硬化最严重的并发症之一。更令人不安的是，从诊断时起的平均预期寿命约为8至10个月。HCC的发病率在美国已经开始增加，主要是由于慢性丙型肝炎（HCV）感染。此外，随着肥胖的流行，包括II型糖尿病和胰岛素抵抗，由于肝硬化的发展，非酒精性脂肪性肝炎（NASH）的出现已经开始在这种毁灭性疾病的发病机制中发挥更大的作用，这是HCC的一个危险因素。最近，医疗保健专业人员普遍关注HCC的增加和缺乏导致或有助于早期诊断和治疗的最佳筛查技术，以期改善这种几乎一致致命的疾病的预后。因此，本研究的目的是验证一种可能用于HCC早期诊断的新标志物。在这方面，我们已经通过单克隆抗体（mAb）结合和表达克隆鉴定了一个在HCC肿瘤中增强的细胞表面蛋白标记物。编码该蛋白的基因已被克隆并被分子鉴定为天冬氨酸（天冬酰胺）-羟化酶（HAAH），该基因在大多数（约90%）乙型肝炎（HBV）和HCV相关的HCC中高表达。此外，这种蛋白似乎存在于这些患者的血清中。因此，我们建立了以重组蛋白为标准，检测血清中C和N末端片段以及全长HAAH的免疫测定方法。由于这种酶在细胞表面表达，我们最近开发了针对该分子不同区域的人单链抗体和IgG抗体。这些试剂将用于人类肝癌小鼠模型中靶向肿瘤的生物分布研究。将有证据支持HAAH基因是HCC的一种新的生物标志物的假设，因为其表达似乎与该疾病的发病机制高度相关。我们计划做以下事情。具体目标验证HAAH作为HCC的生物标志物。具体目标2。进一步表征人scFv片段和抗aah抗体IgG。这些新的基于单抗的检测方法很可能有助于HCC的早期检测，人类抗haah抗体可能被用作特异性检测肝脏中HCC的靶向试剂。