Center for Pancreatic Disease, Division of Gastroenterology Hepatology and Endoscopy, Brigham and Women's Hospital and Department of Medicine, Harvard Medical School, Boston, MA.
Center for Pancreatic Disease, Division of Gastroenterology, Hepatology and Endoscopy, Brigham and Women's Hospital and Department of Medicine, Harvard Medical School, Boston, MA.
J Immunol Methods. 2012 Aug 31;382(1-2):142-149. doi: 10.1016/j.jim.2012.05.018. Epub 2012 Jun 7.
Diagnosis of pancreatic cystic neoplasms remains problematic. We hypothesize that inflammatory mediator proteins in pancreatic cyst fluid can differentiate branch duct intraductal papillary mucinous neoplasms (BD-IPMNs) and pancreatic inflammatory cysts. We aim to 1) detect inflammatory mediator proteins (IMPs) using a multiplexed IMP-targeted microarray in pancreatic cyst fluid obtained during endoscopic ultrasound fine needle aspiration (EUS-FNA) and 2) compare IMP profiles in pancreatic cyst fluid from BD-IPMNs and inflammatory cysts. Pancreatic cyst fluid from ten patients (5 BD-IPMN and 5 inflammatory cysts) was obtained by EUS-FNA and analyzed directly with a multiplexed microarray assay to determine concentrations of 89 IMPs. Statistical analysis was performed using non-parametric methods.
Eighty-three of the 89 assayed IMPs were detected in at least one of the 10 patient samples. Seven IMPs were detected in BD-IPMN but not inflammatory cysts, while eleven IMPs were identified in inflammatory cysts but not BD-IPMN. Notably, granulocyte-macrophage colony-stimulating factor (GM-CSF) expression was present in all five inflammatory cyst samples. Hepatocyte growth factor (HGF) was present in significantly higher concentrations in inflammatory cysts compared to BD-IPMN.
Our exploratory analysis reveals that GM-CSF and HGF in EUS-FNA-collected pancreatic cyst fluid can distinguish between BD-IPMN and inflammatory cyst. Coupling microarray molecular techniques to EUS-FNA may represent a major step forward to our understanding complex pancreatic disease.
胰腺囊性肿瘤的诊断仍然存在问题。我们假设胰腺囊液中的炎症介质蛋白可以区分分支胰管内乳头状黏液性肿瘤(BD-IPMN)和胰腺炎性囊肿。我们旨在 1)使用胰胆管内乳头状黏液性肿瘤(BD-IPMN)和胰腺炎性囊肿患者内镜超声引导下细针抽吸术(EUS-FNA)获得的胰腺囊液中的多重炎症介质蛋白(IMP)靶向微阵列检测炎症介质蛋白(IMP),2)比较胰腺囊液中 BD-IPMN 和炎性囊肿的 IMP 谱。10 例患者(5 例 BD-IPMN 和 5 例炎性囊肿)的胰腺囊液通过 EUS-FNA 获得,并直接用多重微阵列分析检测 89 种 IMP 的浓度。采用非参数方法进行统计分析。
在所检测的 89 种 IMP 中,有 83 种至少在 10 例患者样本中的一种中被检测到。7 种 IMP 仅在 BD-IPMN 中被检测到,而 11 种 IMP 仅在炎性囊肿中被检测到。值得注意的是,所有 5 例炎性囊肿样本均存在粒细胞-巨噬细胞集落刺激因子(GM-CSF)。与 BD-IPMN 相比,炎性囊肿中肝细胞生长因子(HGF)的浓度明显更高。
我们的探索性分析表明,EUS-FNA 收集的胰腺囊液中的 GM-CSF 和 HGF 可以区分 BD-IPMN 和炎性囊肿。将微阵列分子技术与 EUS-FNA 结合可能是我们对复杂胰腺疾病理解的重大进步。