Wang Yuefan, Lih T Mamie, Lee Jae W, Ohtsuka Takao, Hozaka Yuto, Mino-Kenudson Mari, Adsay N Volkan, Luchini Claudio, Scarpa Aldo, Maker Ajay V, Kim Grace E, Paulino Jorge, Chen Lijun, Jiao Liyuan, Sun Zhenyu, Goodman Davina, Pflüger Michael J, Roberts Nicholas J, Matthaei Hanno, Wood Laura D, Furukawa Toru, Zhang Hui, Hruban Ralph H
bioRxiv. 2024 Jul 7:2024.07.07.602385. doi: 10.1101/2024.07.07.602385.
In order to advance our understanding of precancers in the pancreas, 69 pancreatic intraductal papillary neoplasms (IPNs), including 64 intraductal papillary mucinous neoplasms (IPMNs) and 5 intraductal oncocytic papillary neoplasms (IOPNs), 32 pancreatic cyst fluid samples, 104 invasive pancreatic ductal adenocarcinomas (PDACs), 43 normal adjacent tissues (NATs), and 76 macro-dissected normal pancreatic ducts (NDs) were analyzed by mass spectrometry. A total of 10,246 proteins and 22,284 glycopeptides were identified in all tissue samples, and 756 proteins with more than 1.5-fold increase in abundance in IPMNs relative to NDs were identified, 45% of which were also identified in cyst fluids. The over-expression of selected proteins was validated by immunolabeling. Proteins and glycoproteins overexpressed in IPMNs included those involved in glycan biosynthesis and the immune system. In addition, multiomics clustering identified two subtypes of IPMNs. This study provides a foundation for understanding tumor progression and targets for earlier detection and therapies.
This multilevel characterization of intraductal papillary neoplasms of the pancreas provides a foundation for understanding the changes in protein and glycoprotein expression during the progression from normal duct to intraductal papillary neoplasm, and to invasive pancreatic carcinoma, providing a foundation for informed approaches to earlier detection and treatment.
为了加深我们对胰腺癌前病变的理解,我们通过质谱分析了69例胰腺导管内乳头状肿瘤(IPN),包括64例导管内乳头状黏液性肿瘤(IPMN)和5例导管内嗜酸性乳头状肿瘤(IOPN)、32份胰腺囊肿液样本、104例浸润性胰腺导管腺癌(PDAC)、43份正常相邻组织(NAT)以及76份宏观解剖的正常胰腺导管(ND)。在所有组织样本中总共鉴定出10246种蛋白质和22284种糖肽,并且鉴定出756种在IPMN中相对于ND丰度增加超过1.5倍的蛋白质,其中45%也在囊肿液中被鉴定出来。通过免疫标记验证了所选蛋白质的过表达。在IPMN中过表达的蛋白质和糖蛋白包括那些参与聚糖生物合成和免疫系统的蛋白。此外,多组学聚类确定了IPMN的两种亚型。本研究为理解肿瘤进展以及早期检测和治疗的靶点提供了基础。
胰腺导管内乳头状肿瘤的这种多层次特征为理解从正常导管到导管内乳头状肿瘤,再到浸润性胰腺癌进展过程中蛋白质和糖蛋白表达的变化提供了基础,为早期检测和治疗的明智方法提供了基础。