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中文摘要
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描述(由申请人提供):肝细胞癌(HCC)是全球第三大常见癌症死亡原因。HCC是美国增长最快的癌症死亡群体之一,主要是因为丙型肝炎病毒(HCV)感染率的增加。存在一个明显的需要,生物标志物,可以预测那些肝炎阳性的个人发展肝癌在早期阶段时,明确的治疗是潜在的治愈。循环microRNA(miRNAs)作为癌症生物标志物具有巨大的潜力。目前还没有发表的研究已经在HCV感染的患者中鉴定出血清或血浆miRNA特征,这些患者继续发展为HCC。这项研究旨在开发一种循环miRNA签名,用作HCV相关HCC的生物标志物。具体目标1:目标1的目标是鉴定和验证HCV感染个体中HCC的miRNA特征。作为训练集,我们将分析来自HCV阳性个体的血浆样品队列中的miRNA,其中一半是HCC+(马约队列)。然后将在血浆样品的测试组中验证信息量最大的miRNA。具体目标2:目标1中鉴定的一组miRNA将在第二组100份血清样品(EDRN组)中进行验证。大约60%的EDRN参考集为HCV阳性。如果miRNA签名的表现等于或优于血清甲胎蛋白,我们将被授权访问一个更大的EDRN验证集的750个血清样本。这项研究的成功完成将导致在HCC发展之前对HCV感染个体的miRNA特征进行前瞻性收集和评估。
英文摘要
DESCRIPTION (provided by applicant): Hepatocellular carcinoma (HCC) is the third most common cause of cancer death worldwide. HCC is among the fastest growing group of cancer deaths in the U.S mainly because of the increasing rate of hepatitis C viral (HCV)- infections. There exists an obvious need for biomarkers that could predict those hepatitis positive individuals who develop HCC at early stages when definitive therapy is potentially curative. Circulating microRNAs (miRNAs) hold great potential as cancer biomarkers. There are no published studies that have identified a serum or plasma miRNA signature in HCV infected patients that go on to develop HCC. This research aims to develop a circulating miRNA signature to be used as biomarkers for HCV-associated HCC. Specific Aim 1: The goal of Aim 1 is to identify and validate a miRNA signature for HCC in HCV-infected individuals. As the training set, we will profile miRNAs in a cohort of plasma samples from HCV positive individuals, half of which are HCC+ (Mayo cohort). The most informative miRNAs will then be validated in a testing set of plasma samples. Specific Aim 2: The panel of miRNAs identified in Aim 1 will be validated in a second cohort of 100 serum samples (EDRN cohort). Approximately 60% of the EDRN reference set is HCV positive. Should the miRNA signature perform equal to or better than that of serum alpha fetoprotein, we will be granted access to a larger EDRN validation set of 750 serum samples. Successful completion of this research will lead to prospective collection and evaluation of the miRNA signature in HCV-infected individuals prior to the development of HCC.
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会议论文
miR-221 regulates CD44 in hepatocellular carcinoma through the PI3K-AKT-mTOR pathway.
miR-221通过PI3K-AKT-MTOR途径调节肝细胞癌中的CD44。
DOI: 10.1016/j.bbrc.2017.04.121
发表时间: 2017-06-03
期刊: Biochemical and biophysical research communications
影响因子: 3.1
作者: [Kim J, Jiang J, Badawi M, Schmittgen TD]
通讯作者: Schmittgen TD
R21 MPI microRNA directed therapy for treating early stage pancreatic cancer
  • 批准号:
    10577609
  • 项目类别:
  • 资助金额:
    $17.82万
  • 财政年份:
    2023
  • 负责人:
    THOMAS D. SCHMITTGEN
  • 依托单位:
Pilot Project 3: Contribution of Racial Disparity towards the Early Development of Pancreatic Cancer
  • 批准号:
    10006214
  • 项目类别:
  • 资助金额:
    $11.3万
  • 财政年份:
    2018
  • 负责人:
    THOMAS D. SCHMITTGEN
  • 依托单位:
Project 3 ADM
  • 批准号:
    10762126
  • 项目类别:
  • 资助金额:
    $11.6万
  • 财政年份:
    2018
  • 负责人:
    THOMAS D. SCHMITTGEN
  • 依托单位:
miRNA Biomarkers for Hepatocellular Carcinoma Associated with Viral Hepatitis
  • 批准号:
    8364566
  • 项目类别:
  • 资助金额:
    $25.1万
  • 财政年份:
    2012
  • 负责人:
    THOMAS D. SCHMITTGEN
  • 依托单位:
海外基金