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胃肠胰内分泌肿瘤的分子特征

Molecular profiles of gastroenteropancreatic endocrine tumors.

作者信息

Perren Aurel, Anlauf Martin, Komminoth Paul

机构信息

Department of Pathology, University Hospital Zürich, Zurich, Switzerland.

出版信息

Virchows Arch. 2007 Aug;451 Suppl 1:S39-46. doi: 10.1007/s00428-007-0449-9. Epub 2007 Aug 8.

DOI:10.1007/s00428-007-0449-9
PMID:17684763
Abstract

Neuroendocrine tumors of the gastroenteropancreatic system are defined by their endocrine phenotype and share many histopathological and clinical features. However, the fact that the hormone production of tumors depends on their site of origin, that the tumors differ in their biology, and that the association with familial syndromes is nonrandom suggests heterogeneity. It is therefore conceivable that the gastroenteropancreatic neuroendocrine tumors also differ in their molecular profile. This review summarizes and discusses the available data in this field.

摘要

胃肠胰系统神经内分泌肿瘤由其内分泌表型定义,并具有许多组织病理学和临床特征。然而,肿瘤的激素产生取决于其起源部位、肿瘤在生物学上存在差异以及与家族综合征的关联并非随机,这些事实表明存在异质性。因此,可以想象胃肠胰神经内分泌肿瘤在分子特征上也存在差异。本综述总结并讨论了该领域的现有数据。

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The ENETS/WHO grading system for neuroendocrine neoplasms of the gastroenteropancreatic system: a review of the current state, limitations and proposals for modifications.胃肠胰系统神经内分泌肿瘤的ENETS/WHO分级系统:现状、局限性及修改建议综述
Int J Endocr Oncol. 2016 Aug;3(3):203-219. doi: 10.2217/ije-2016-0006. Epub 2016 Jul 14.
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Site-specific biology and pathology of gastroenteropancreatic neuroendocrine tumors.胃肠胰神经内分泌肿瘤的部位特异性生物学与病理学
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本文引用的文献

1
Analysis of molecular pathways in sporadic neuroendocrine tumors of the gastro-entero-pancreatic system.胃肠胰系统散发性神经内分泌肿瘤的分子通路分析
Int J Cancer. 2007 May 15;120(10):2157-64. doi: 10.1002/ijc.22569.
2
Multiple endocrine neoplasia type 1 (MEN1): loss of one MEN1 allele in tumors and monohormonal endocrine cell clusters but not in islet hyperplasia of the pancreas.1型多发性内分泌肿瘤(MEN1):肿瘤及单激素内分泌细胞簇中一个MEN1等位基因缺失,但胰腺胰岛增生中无此现象。
J Clin Endocrinol Metab. 2007 Mar;92(3):1118-28. doi: 10.1210/jc.2006-1944. Epub 2006 Dec 19.
3
Molecular parameters associated with insulinoma progression: chromosomal instability versus p53 and CK19 status.
与胰岛素瘤进展相关的分子参数:染色体不稳定性与p53及细胞角蛋白19状态的比较
Cytogenet Genome Res. 2006;115(3-4):289-97. doi: 10.1159/000095926.
4
Novel candidate tumour suppressor gene loci on chromosomes 11q23-24 and 22q13 involved in human insulinoma tumourigenesis.涉及人类胰岛素瘤肿瘤发生的位于11号染色体q23 - 24和22号染色体q13上的新型候选肿瘤抑制基因位点。
J Pathol. 2006 Dec;210(4):450-8. doi: 10.1002/path.2072.
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Identification of potential therapeutic targets by gene-expression profiling in pancreatic endocrine tumors.
Gastroenterology. 2006 Nov;131(5):1597-610. doi: 10.1053/j.gastro.2006.09.007. Epub 2006 Sep 8.
6
Nuclear translocation of beta-catenin protein but absence of beta-catenin and APC mutation in gastrointestinal carcinoid tumor.β-连环蛋白的核转位,但在胃肠道类癌肿瘤中不存在β-连环蛋白和APC突变。
Ann Surg Oncol. 2006 Dec;13(12):1604-9. doi: 10.1245/s10434-006-9072-2. Epub 2006 Sep 29.
7
Gene expression profiles of progressive pancreatic endocrine tumours and their liver metastases reveal potential novel markers and therapeutic targets.进展期胰腺内分泌肿瘤及其肝转移灶的基因表达谱揭示了潜在的新型标志物和治疗靶点。
Endocr Relat Cancer. 2006 Jun;13(2):541-58. doi: 10.1677/erc.1.01153.
8
BRAF gene mutations are rare events in gastroenteropancreatic neuroendocrine tumors.BRAF基因突变在胃肠胰神经内分泌肿瘤中是罕见事件。
Am J Clin Pathol. 2005 Feb;123(2):256-60.
9
BRAF and endocrine tumors: mutations are frequent in papillary thyroid carcinomas, rare in endocrine tumors of the gastrointestinal tract and not detected in other endocrine tumors.
Endocr Relat Cancer. 2004 Dec;11(4):855-60. doi: 10.1677/erc.1.00841.
10
Microsatellite instability and gene mutations in transforming growth factor-beta type II receptor are absent in small bowel carcinoid tumors.小肠类癌肿瘤不存在微卫星不稳定性和转化生长因子-βⅡ型受体基因突变。
Cancer. 2005 Jan 15;103(2):229-36. doi: 10.1002/cncr.20750.