Development of Novel Markers for Melanoma Progression

黑色素瘤进展的新型标记物的开发

• 批准号: 7460923
• 负责人: Byungwoo Ryu
• 金额: $ 0.12万
• 依托单位: JOHNS HOPKINS UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-07-01 至 2008-09-14
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7460923
• 关键词: Affect; Algorithms; Biochemical; Bioinformatics; Biological Markers; Breslow Thickness; Cancer Center; Candidate Disease Gene; Case Study; Cell Line; Collection; Computer Analysis; Data; Databases; Depth; Development; Diagnostic; Disease; Disease Outcome; Disease Progression; Doctor of Philosophy; Early Diagnosis; Event; Freezing; Gene Expression; Gene Expression Profiling; Gene Silencing; Genes; Genetic; Genome Stability; Genomic Instability; Goals; Growth; Hereditary Melanoma; Human; Immunohistochemistry; In Situ; In Situ Hybridization; Incidence; Individual; Laboratories; Lead; Length; Lesion; Life Expectancy; Malignant Neoplasms; Malignant neoplasm of pancreas; Melanoma Cell; Mentors; Metastatic to; Microarray Analysis; Molecular; Molecular Profiling; Mutation; Outcome; Patients; Phase; Postdoctoral Fellow; Precancerous melanosis; Primary Neoplasm; Principal Investigator; Property; Proteins; Radial; Rate; Research; Research Personnel; Research Proposals; Research Training; Resources; Retrospective Studies; Sampling; Selection Criteria; Series; Specificity; Specimen; Staging; System; Systemic Therapy; Techniques; Telomerase; Testing; Tissue Banks; Tissue Microarray; Training; Transcription Regulatory Protein; Tumor Cell Invasion; Tumor Markers; United States; Validation; base; career; cell growth; density; design; experience; gene discovery; improved; lifetime risk; melanocyte; melanoma; novel; novel diagnostics; prognostic; programs; research study; response; telomere; therapeutic target; tool; transcription factor

DESCRIPTION (provided by applicant): The candidate is currently a Research Associate in the Sidney Kimmel Cancer Center at Johns Hopkins who has previously spearheaded efforts towards discovery of new pancreatic cancer markers and the identification of invasion-specific genes in pancreatic cancers in the laboratory of Dr. Scott Kern at Johns Hopkins. The long-term career objectives of the candidate are to develop early detection markers and identify therapeutic targets for human melanoma. This research proposal uses both a mentored research training period (years 1-3) and an independent training period (years 4-5) in order for the investigator to develop gene discovery systems for human melanoma under the guidance of Drs. Rhoda Alani and Scott Kern. The investigator already has early data on promising new diagnostic/prognostic melanoma tumor markers (the HLH transcription factor, Id1 and in-situ telomere length) and therapeutic targets (Id1, telomerase) in melanoma and those will be developed as part of this proposal. The specific aims are, therefore: 1) to identify novel markers and therapeutic targets for melanoma using gene profiling of human melanoma cell lines and primary human melanomas from varying stages of disease progression in combination with experiment-oriented data reduction algorism; 2) to determine the diagnostic/prognostic significance of Id1 expression in melanocytic lesions and its utility as an indicator of malignancy and therapeutic target; 3) To evaluate in-situ telomere lengths in archival samples of melanomas and determine the diagnostic/prognostic utility of telomere length in predicting biologic outcomes of melanomas in a retrospective study. The overall goal of the investigator is to transition from research in the molecular characterization of pancreatic cancers to analogous studies in human melanoma. Since melanoma is the fastest growing malignancy in the U.S. and there are no therapies that have been shown to increase life expectancy for patients with advanced disease, it is anticipated that these studies will be of high impact.

描述（由申请人提供）：该候选人目前是约翰霍普金斯大学Sidney Kimmel癌症中心的研究助理，曾在约翰霍普金斯大学Scott Kern博士的实验室中率先发现新的胰腺癌标志物和胰腺癌侵袭特异性基因。候选人的长期职业目标是开发早期检测标记并确定人类黑色素瘤的治疗靶点。本研究计划采用有导师指导的研究培训期（1-3年）和独立培训期（4-5年），在博士的指导下开发人类黑色素瘤基因发现系统。罗达·阿拉尼和斯科特·科恩。研究者已经获得了有希望的黑色素瘤新诊断/预后肿瘤标志物（HLH转录因子，Id1和原位端粒长度）和治疗靶点（Id1，端粒酶）的早期数据，这些将作为该提案的一部分进行开发。因此，具体目标是：1)利用人类黑色素瘤细胞系和不同疾病进展阶段的原发性人类黑色素瘤的基因谱分析，结合以实验为导向的数据约简算法，确定黑色素瘤的新标记物和治疗靶点；2)确定Id1表达在黑色素细胞病变中的诊断/预后意义及其作为恶性肿瘤和治疗靶点的指标；3)在一项回顾性研究中评估黑素瘤档案样本的原位端粒长度，并确定端粒长度在预测黑素瘤生物学预后方面的诊断/预后效用。研究者的总体目标是从胰腺癌分子特征的研究过渡到人类黑色素瘤的类似研究。由于黑色素瘤是美国增长最快的恶性肿瘤，并且没有任何治疗方法被证明可以提高晚期疾病患者的预期寿命，因此预计这些研究将具有很高的影响。