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首页> 外文期刊>Annals of Surgical Oncology >Principal Component Analysis, Hierarchical Clustering, and Decision Tree Assessment of Plasma mRNA and Hormone Levels as an Early Detection Strategy for Small Intestinal Neuroendocrine (Carcinoid) Tumors
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Principal Component Analysis, Hierarchical Clustering, and Decision Tree Assessment of Plasma mRNA and Hormone Levels as an Early Detection Strategy for Small Intestinal Neuroendocrine (Carcinoid) Tumors

机译:主成分分析,层次聚类和决策树评估血浆mRNA和激素水平,作为小肠神经内分泌(类癌)肿瘤的早期发现策略

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摘要

Incidence of neuroendocrine tumors (NETs) is increasing (approximately 6%/year), but clinical presentation is nonspecific, resulting in delays in diagnosis (5–7 years; approximately 70% have metastases). This reflects absence of a sensitive plasma marker. The aim of this study is to investigate whether detection of circulating messenger RNA (mRNA) alone or in combination with circulating NET-related hormones and growth factors can detect gastrointestinal NET disease. The small intestinal (SI) NET cell line KRJ-I was used to define the sensitivity of real-time polymerase chain reaction (PCR) for mRNA detection in blood. NSE, Tph-1, and VMAT 2 transcripts were identified from one KRJ-I cell/ml blood. mRNA from the tissue and plasma of SI-NETs (n = 12) and gastric NETs (n = 7), and plasma from healthy controls (n = 9) was isolated and real-time PCR performed. Tph-1 was a specific marker of SI-NETs (58%, p < 0.03) whereas CgA transcripts did not differentiate tumors from controls. Patients with metastatic disease expressed more marker transcripts than localized tumors (75% versus 18%, p < 0.02). Plasma 5-hydroxytryptamine (5-HT), chromogranin A (CgA), ghrelin, and connective tissue growth factor (CTGF) fragments were measured, combined with mRNA levels, and a predictive mathematical model for NET diagnosis developed using decision trees. The sensitivity and specificity to diagnose SI-NETs and gastric NETs were 81.2% and 100%, and 71.4% and 55.6%, respectively. We conclude that mRNA from one NET cell/ml blood can be detected. Circulating plasma Tph-1 is a promising marker gene for SI-NET disease (specificity 100%) while an increased number of marker transcripts (>2) correlated with disease spread. Including NET-related circulating hormones and growth factors in the algorithm increased the sensitivity of detection of SI-NETs from 58 to 82%.
机译:神经内分泌肿瘤(NETs)的发病率正在增加(大约6%/年),但是临床表现是非特异性的,导致诊断延迟(5-7年;大约70%有转移)。这反映出不存在敏感的血浆标志物。这项研究的目的是调查单独检测循环信使RNA(mRNA)或与循环NET相关的激素和生长因子联合检测是否可以检测胃肠道NET疾病。小肠(SI)NET细胞系KRJ-1用于定义实时聚合酶链反应(PCR)对血液中mRNA检测的敏感性。从一种KRJ-1细胞/ ml血液中鉴定出NSE,Tph-1和VMAT 2 转录本。分离出来自SI-NET(n = 12)和胃NET(n = 7)的组织和血浆的mRNA,以及来自健康对照组(n = 9)的血浆,并进行实时PCR。 Tph-1是SI-NETs的特异性标记物(58%,p <0.03),而CgA转录本不能将肿瘤与对照区分开。转移性疾病患者比局部肿瘤表达更多的标志物转录物(75%比18%,p <0.02)。测量血浆5-羟色胺(5-HT),嗜铬粒蛋白A(CgA),生长素释放肽和结缔组织生长因子(CTGF)片段,并与mRNA水平结合,并使用决策树开发用于NET诊断的预测数学模型。诊断SI-NET和胃NET的敏感性和特异性分别为81.2%和100%,以及71.4%和55.6%。我们得出的结论是,可以检测到来自一个NET细胞/ ml血液的mRNA。循环血浆Tph-1是SI-NET疾病的有前途的标志物基因(特异性为100%),而标志物转录物的数量增加(> 2)与疾病传播相关。该算法中包括NET相关的循环激素和生长因子,将SI-NET的检测灵敏度从58%提高到82%。

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  • 来源
    《Annals of Surgical Oncology》 |2009年第2期|487-498|共12页
  • 作者单位

    Department of Gastroenterological Surgery Yale University School of Medicine 333 Cedar Street P.O. Box 208062 New Haven CT 06520-8062 USA;

    Department of Gastroenterological Surgery Yale University School of Medicine 333 Cedar Street P.O. Box 208062 New Haven CT 06520-8062 USA;

    Department of Gastroenterological Surgery Yale University School of Medicine 333 Cedar Street P.O. Box 208062 New Haven CT 06520-8062 USA;

    Department of Computer Science and Applied Mathematics Weizmann Institute of Science Rehovot 76100 Israel;

    Institute of Pathophysiology and Immunology Centre for Molecular Medicine Medical University of Graz Graz Austria;

    Department of Gastroenterological Surgery Yale University School of Medicine 333 Cedar Street P.O. Box 208062 New Haven CT 06520-8062 USA;

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