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Molecular Alterations in Exocrine Neoplasms of the Pancreas

机译:胰腺外分泌肿瘤的分子改变

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CONTEXT: Pancreatic cancer is one of the leading causes of cancer-related deaths. Most cases are diagnosed at an advanced stage when the disease is beyond surgical intervention. Molecular studies during the past decade have contributed greatly to our understanding of this disease. Various germ-line and somatic mutations associated with pancreatic cancers have been characterized, along with abnormal variations in the gene expression patterns. A thorough characterization of molecular alterations such as genetic and epigenetic changes, alterations in the expression of genes and changes in proteins, and posttranslational modifications in pancreatic cancer could lead to a better understanding of its pathogenesis. OBJECTIVE: To provide an overview of the various molecular alterations in pancreatic cancer and the methodologies used to catalog such alterations. DATA SOURCES: Published studies about various molecular alterations at the genomic, epigenetic, transcriptomic, and proteomic levels in pancreatic cancer. CONCLUSIONS: The available data from pancreatic cancer suggests that there are a large number of molecular alterations at genomic, epigenetic, transcriptomic, and proteomic levels. It is now possible to initiate a systems approach to studying pancreatic cancer especially in light of newer initiatives to dissect the pancreatic cancer genome.
机译:背景:胰腺癌是与癌症相关的死亡的主要原因之一。当疾病超出手术干预范围时,大多数病例被诊断为晚期。在过去的十年中,分子研究为我们对这种疾病的理解做出了巨大贡献。与胰腺癌相关的各种种系和体细胞突变,以及基因表达模式的异常变异,都得到了表征。对分子变化的全面表征,例如遗传和表观遗传学变化,基因表达变化和蛋白质变化,以及胰腺癌的翻译后修饰,可以使人们更好地了解其发病机理。目的:概述胰腺癌的各种分子变化及其分类方法。数据来源:已发表的有关胰腺癌基因组,表观遗传学,转录组学和蛋白质组学水平的各种分子改变的研究。结论:胰腺癌的现有数据表明,在基因组,表观遗传学,转录组学和蛋白质组学水平上存在大量分子改变。现在有可能启动一种研究胰腺癌的系统方法,尤其是根据剖析胰腺癌基因组的新举措。

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    《Archives of Pathology & Laboratory Medicine》 |2009年第3期|p.405-412|共8页
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    Prathibha Ranganathan, PhD, H. C. Harsha, MSc, Akhilesh Pandey, MD, PhDAccepted for publication October 6, 2008.From the Institute of Bioinformatics, International Technology Park, Bangalore, India (Dr Ranganathan and Mr Harsha), Manipal University, Manipal, Karnataka, India (Mr Harsha), the McKusick-Nathans Institute of Genetic Medicine and the Departments of Biological Chemistry (Mr Harsha and Dr Pandey) and Pathology and Oncology (Dr Pandey), The Johns Hopkins University, Baltimore, Maryland.The authors have no relevant financial interest in the products or companies described in this article.Reprints: Akhilesh Pandey, MD, PhD, The Johns Hopkins University, McKusick-Nathans Institute of Genetic Medicine, 733 N Broadway, BRB 527, Baltimore, MD 21205 (e-mail: pandey@jhmi.edu).,;

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