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本文引用的文献

1
Frequent activating GNAS mutations in villous adenoma of the colorectum.结直肠绒毛状腺瘤中频繁出现的激活型 GNAS 突变。
J Pathol. 2012 Sep;228(1):113-8. doi: 10.1002/path.4012. Epub 2012 Jul 2.
2
Oncogenic Kras is required for both the initiation and maintenance of pancreatic cancer in mice.致癌性 Kras 基因对于小鼠胰腺癌细胞的起始和维持都是必需的。
J Clin Invest. 2012 Feb;122(2):639-53. doi: 10.1172/JCI59227. Epub 2012 Jan 9.
3
Presence of somatic mutations in most early-stage pancreatic intraepithelial neoplasia.大多数早期胰腺上皮内瘤变中存在体细胞突变。
Gastroenterology. 2012 Apr;142(4):730-733.e9. doi: 10.1053/j.gastro.2011.12.042. Epub 2012 Jan 5.
4
The antidiabetic drug metformin inhibits gastric cancer cell proliferation in vitro and in vivo.二甲双胍这种抗糖尿病药物能够在体外和体内抑制胃癌细胞的增殖。
Mol Cancer Ther. 2012 Mar;11(3):549-60. doi: 10.1158/1535-7163.MCT-11-0594. Epub 2012 Jan 5.
5
Detection of KRAS gene mutations in endoscopic ultrasound-guided fine-needle aspiration biopsy for improving pancreatic cancer diagnosis.经内镜超声引导下细针穿刺活检术检测 KRAS 基因突变对提高胰腺癌诊断的价值。
Am J Gastroenterol. 2011 Dec;106(12):2104-11. doi: 10.1038/ajg.2011.281. Epub 2011 Aug 30.
6
Fluorescence in situ hybridization and K-ras analyses improve diagnostic yield of endoscopic ultrasound-guided fine-needle aspiration of solid pancreatic masses.荧光原位杂交和 K-ras 分析提高了内镜超声引导下细针抽吸胰腺实性肿块的诊断产量。
Pancreas. 2011 Oct;40(7):1057-62. doi: 10.1097/MPA.0b013e3182200201.
7
MicroRNA-10b expression correlates with response to neoadjuvant therapy and survival in pancreatic ductal adenocarcinoma.微小 RNA-10b 的表达与胰腺导管腺癌对新辅助治疗的反应和生存相关。
Clin Cancer Res. 2011 Sep 1;17(17):5812-21. doi: 10.1158/1078-0432.CCR-11-0695. Epub 2011 Jun 7.
8
Mucin expression pattern in pancreatic diseases: findings from EUS-guided fine-needle aspiration biopsies.在胰腺疾病中黏蛋白表达模式:EUS 引导下细针穿刺活检的结果。
Am J Gastroenterol. 2011 Jul;106(7):1359-63. doi: 10.1038/ajg.2011.22. Epub 2011 Jun 7.
9
The usefulness of S100P, mesothelin, fascin, prostate stem cell antigen, and 14-3-3 sigma in diagnosing pancreatic adenocarcinoma in cytological specimens obtained by endoscopic ultrasound guided fine-needle aspiration.S100P、间皮素、成束蛋白、前列腺干细胞抗原和14-3-3西格玛在通过内镜超声引导下细针穿刺获取的细胞学标本中诊断胰腺腺癌的效用。
Diagn Cytopathol. 2014 Mar;42(3):193-9. doi: 10.1002/dc.21684. Epub 2011 Apr 28.
10
Role of endoscopic ultrasound-guided fine needle aspiration (EUS-FNA) for diagnosis of solid pancreatic masses.内镜超声引导下细针抽吸术(EUS-FNA)在诊断胰腺实性肿块中的作用。
Dig Endosc. 2011 May;23 Suppl 1:29-33. doi: 10.1111/j.1443-1661.2011.01112.x.

采用超声内镜引导下细针穿刺获取标本的分子生物学方法诊断胰腺癌。

Molecular Biologic Approach to the Diagnosis of Pancreatic Carcinoma Using Specimens Obtained by EUS-Guided Fine Needle Aspiration.

机构信息

Department of Gastroenterology and Neurology, Faculty of Medicine, Kagawa University, 1750-1 Ikenobe, Miki-cho, Kita-gun, Kagawa Prefecture, Takamatsu 761-0793, Japan.

出版信息

Gastroenterol Res Pract. 2012;2012:243524. doi: 10.1155/2012/243524. Epub 2012 Nov 8.

DOI:10.1155/2012/243524
PMID:23197977
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3503278/
Abstract

We review the utility of endoscopic ultrasound-guided fine needle aspiration (EUS-FNA), a rapid, safe, cost-effective, and accurate diagnostic modality for evaluating pancreatic tumors. EUS-FNA is currently used for the diagnosis and staging of pancreatic tumors. The sensitivity of EUS-FNA for pancreatic malignancy ranges from 75% to 94%, and its specificity approaches 100% in most studies. However, EUS-FNA has some limitations in the diagnosis of well-differentiated or early-stage cancers. Recent evidence suggests that molecular biological analysis using specimens obtained by EUS-FNA improves diagnostic sensitivity and specificity, especially in borderline cytological cases. It was also reported that additional information regarding patient response to chemotherapy, surgical resectability, time to metastasis, and overall survival was acquired from the genetic analysis of specimens obtained by EUS-FNA. Other studies have revealed that the analysis of KRAS, MUC, p53, p16, S100P, SMAD4, and microRNAs is helpful in making the diagnosis of pancreatic carcinoma. In this paper, we describe the present state of genetic diagnostic techniques for use with EUS-FNA samples in pancreatic diseases. We also discuss the role of molecular biological analyses for the diagnosis of pancreatic carcinoma.

摘要

我们回顾了内镜超声引导下细针抽吸(EUS-FNA)的实用性,EUS-FNA 是一种快速、安全、具有成本效益且准确的诊断胰腺肿瘤的方法。EUS-FNA 目前用于胰腺肿瘤的诊断和分期。在大多数研究中,EUS-FNA 对胰腺恶性肿瘤的敏感性为 75%至 94%,特异性接近 100%。然而,EUS-FNA 在诊断分化良好或早期癌症方面存在一些局限性。最近的证据表明,使用 EUS-FNA 获得的标本进行分子生物学分析可提高诊断的敏感性和特异性,尤其是在临界细胞学病例中。据报道,还从 EUS-FNA 获得的标本的基因分析中获得了有关患者对化疗的反应、手术可切除性、转移时间和总体生存率的其他信息。其他研究表明,KRAS、MUC、p53、p16、S100P、SMAD4 和 microRNAs 的分析有助于诊断胰腺癌。在本文中,我们描述了用于胰腺疾病的 EUS-FNA 样本的遗传诊断技术的现状。我们还讨论了分子生物学分析在诊断胰腺癌中的作用。