Analysis of LC-MS data to identify peptide and glycan biomarkers for hepatocellul

分析 LC-MS 数据以鉴定肝细胞的肽和聚糖生物标志物

• 批准号: 7899433
• 负责人: Habtom W Ressom
• 金额: $ 28.67万
• 依托单位: GEORGETOWN UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-09-01 至 2015-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7899433
• 关键词: Accounting; Address; Behavior; Biochemistry; Bioinformatics; Biological; Biological Assay; Biological Markers; Biometry; Blood specimen; Chronic; Cirrhosis; Collaborations; Communities; Complex; Computer software; Computing Methodologies; Coupled; Data; Detection; Development; Diagnosis; Diagnostic; Disease; Disease Management; Early Diagnosis; Egypt; Ensure; Exhibits; Fibrosis; Goals; Health; Heterogeneity; Human; Individual; Isotopes; Knowledge; Label; Lead; Liver diseases; Machine Learning; Malignant Neoplasms; Maps; Mass Spectrum Analysis; Methods; Metric; Michigan; Modeling; Molecular Profiling; Newly Diagnosed; Patients; Pattern; Peptides; Performance; Plasma; Polysaccharides; Population; Primary carcinoma of the liver cells; Process; Proteins; Recruitment Activity; Research; Running; Sampling; Screening for cancer; Screening procedure; Serum; Solutions; Source; Staging; Subgroup; System; Technology; Testing; United States; Universities; University Hospitals; Work; analytical tool; base; comparative; design; disease classification; disorder control; high risk; improved; instrument; liquid chromatography mass spectrometry; mass spectrometer; multiple reaction monitoring; novel; open source; patient population; public health relevance; sample collection; stem; synthetic peptide; tool; treatment strategy

DESCRIPTION (provided by applicant): Early detection of cancer improves patient survival. Characterizing the association of peptides and glycans with cancer is one of the most promising strategies to discover early-diagnosis cancer biomarkers. This study evaluates peptide and glycan expression profiles in the progression of chronic liver disease (CLD) to hepatocellular carcinoma (HCC) by using the liquid chromatography-mass spectrometry (LC-MS) technology. The goal is to find and validate peptide and glycan biomarkers for detection of HCC at a treatable stage in a high-risk population of patients with CLD. Label-free LC-MS quantification allows comparison of peptides and glycans with good throughput which allows us to compare a large population of patients. However, such quantification is not addressed adequately in the instrument-specific software packages. In particular, alignment and normalization of LC-MS data present a significant challenge in label-free quantification and comparison of biomolecules. This challenge coupled with biological variability and disease heterogeneity in human populations has restricted recent advances in LC-MS-based biomarker discovery studies. This project brings together experts in bioinformatics, biostatistics, biochemistry, and mass spectrometry to develop a suite of novel analytical tools for LC-MS-based label-free quantification and comparison of peptides and glycans in serum and plasma. Specifically, a novel Bayesian hierarchical model will be investigated for simultaneous alignment and normalization of LC-MS data and for identification of patient subgroups. The Bayesian framework involves fixed and random effects to account for subpopulation homogeneous behavior (fixed systematic changes), while allowing for modeling heterogeneity within a group (random effects). A spike-in study will be conducted to obtain replicate LC-MS runs with known peptide and glycan concentrations. The data will be utilized to develop and optimize the proposed Bayesian framework and to compare its performance with other existing solutions. The optimized framework and a machine learning-based feature selection method will be applied to identify an integrated set of peptide and glycan candidate biomarkers for early detection of HCC. LC-MS analysis of integrated peptides and glycans in both serum and plasma of patients with HCC is to our knowledge unprecedented. Blood samples from patients with HCC and CLD controls in Egypt and United States will be used. The biomarkers will be validated using isotope dilution mass spectrometric assays. PUBLIC HEALTH RELEVANCE: This project will lead to the development of a suite of novel open source analytical tools for label-free quantification of peptides and glycans in serum and plasma using liquid chromatography-mass spectrometry (LC-MS) technologies. The availability of such tools will assist the research community in advancing the promising LC-MS-based biomarker discovery research. The proposed tools will be utilized to find and validate early-diagnosis biomarkers of hepatocellular carcinoma (HCC). Defining clinically applicable biomarkers that detect early-stage HCC in a high-risk population of patients with chronic liver disease has potentially far-reaching consequences for disease management and patient health. This project is important because most HCC patients are diagnosed at a late stage, where the treatment options are limited. There is a pressing need to identify biomarkers of HCC that could be used for early detection and more accurate classification of disease. In addition to screening high-risk populations for early signs of disease, the resulting biomarkers could be used to design and test improved treatment strategies.

描述（由申请人提供）：癌症的早期检测可提高患者的生存率。表征肽和聚糖与癌症的关联是发现早期诊断癌症生物标志物的最有前途的策略之一。本研究采用液相色谱-质谱联用技术（LC-MS）对慢性肝病（CLD）发展为肝细胞癌（HCC）过程中的肽和聚糖表达谱进行了评估。目的是寻找和验证肽和聚糖生物标志物，用于在CLD患者的高风险人群中检测可治疗阶段的HCC。无标记LC-MS定量允许以良好的通量比较肽和聚糖，这使我们能够比较大量患者。然而，这种量化在仪器专用软件包中没有得到充分解决。特别是，LC-MS数据的比对和标准化在生物分子的无标记定量和比较中提出了重大挑战。这一挑战加上人类群体中的生物变异性和疾病异质性限制了基于LC-MS的生物标志物发现研究的最新进展。该项目汇集了生物信息学、生物统计学、生物化学和质谱学方面的专家，开发了一套新的分析工具，用于血清和血浆中肽和聚糖的基于LC-MS的无标记定量和比较。具体而言，将研究一种新的贝叶斯分层模型，用于LC-MS数据的同步比对和标准化以及患者亚组的识别。贝叶斯框架涉及固定和随机效应，以解释亚群同质行为（固定系统变化），同时允许对组内异质性（随机效应）进行建模。将进行加标研究，以获得具有已知肽和聚糖浓度的重复LC-MS运行。这些数据将用于开发和优化拟议的贝叶斯框架，并将其性能与其他现有解决方案进行比较。优化的框架和基于机器学习的特征选择方法将被应用于识别用于早期检测HCC的肽和聚糖候选生物标志物的集成集合。据我们所知，HCC患者血清和血浆中整合肽和聚糖的LC-MS分析是前所未有的。将使用来自埃及和美国HCC患者和CLD对照的血液样本。将使用同位素稀释质谱测定法对生物标志物进行验证。 公共卫生相关性：该项目将开发一套新型开源分析工具，用于使用液相色谱-质谱（LC-MS）技术对血清和血浆中的肽和聚糖进行无标记定量。这些工具的可用性将有助于研究界推进有前途的基于LC-MS的生物标志物发现研究。所提出的工具将用于寻找和验证肝细胞癌（HCC）的早期诊断生物标志物。定义临床适用的生物标志物，检测慢性肝病患者高危人群中的早期HCC，对疾病管理和患者健康具有潜在的深远影响。这个项目很重要，因为大多数HCC患者都是在晚期被诊断出来的，治疗选择有限。目前迫切需要鉴定HCC的生物标志物，以用于早期检测和更准确的疾病分类。除了筛查高风险人群的早期疾病迹象外，由此产生的生物标志物可用于设计和测试改进的治疗策略。