Cyst fluid glycoproteins accurately distinguishing malignancies of pancreatic cystic neoplasm

被引:4
作者
Cui, Ming [1 ]
Hu, Ya [1 ]
Zhang, Zejian [2 ]
Chen, Tianqi [2 ]
Dai, Menghua [1 ]
Xu, Qiang [1 ]
Guo, Junchao [1 ]
Zhang, Taiping [1 ]
Liao, Quan [1 ]
Yu, Jun [3 ,4 ]
Zhao, Yupei [1 ]
机构
[1] Chinese Acad Med Sci & Peking Union Med Coll, Natl Sci & Technol Key Infrastruct Translat Med, Peking Union Med Coll Hosp, Dept Gen Surg,Key Lab Res Pancreat Tumor,State Key, Beijing 100730, Peoples R China
[2] Chinese Acad Med Sci & Peking Union Med Coll, Natl Sci & Technol Key Infrastruct Translat Med, Peking Union Med Coll Hosp, Dept Med Res Ctr,State Key Lab Complex Severe & Ra, Beijing 100730, Peoples R China
[3] Johns Hopkins Univ, Dept Med Oncol & Surg, Sch Med, Baltimore, MD 21224 USA
[4] Tianjin Med Univ Canc Inst & Hosp, Pancreas Ctr, Tianjin 300060, Peoples R China
基金
北京市自然科学基金;
关键词
CARCINOEMBRYONIC ANTIGEN; GLYCOSYLATION; REPRESENTS; MANAGEMENT; DIAGNOSIS;
D O I
10.1038/s41392-023-01645-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Pancreatic cystic neoplasms (PCNs) are recognized as precursor lesions of pancreatic cancer, with a marked increase in prevalence. Early detection of malignant PCNs is crucial for improving prognosis; however, current diagnostic methods are insufficient for accurately identifying malignant PCNs. Here, we utilized mass spectrometry (MS)-based glycosite- and glycoform-specific glycoproteomics, combined with proteomics, to explore potential cyst fluid diagnostic biomarkers for PCN. The glycoproteomic and proteomic landscape of pancreatic cyst fluid samples from PCN patients was comprehensively investigated, and its characteristics during the malignant transformation of PCN were analyzed. Under the criteria of screening specific cyst fluid biomarkers for the diagnosis of PCN, a group of cyst fluid glycoprotein biomarkers was identified. Through parallel reaction monitoring (PRM)-based targeted glycoproteomic analysis, we validated these chosen glycoprotein biomarkers in a second cohort, ultimately confirming N-glycosylated PHKB (Asn-935, H5N2F0S0; Asn-935, H4N4F0S0; Asn-935, H5N4F0S0), CEACAM5 (Asn-197, H5N4F0S0) and ATP6V0A4 (Asn-367, H6N4F0S0) as promising diagnostic biomarkers for distinguishing malignant PCNs. These glycoprotein biomarkers exhibited robust performance, with an area under the curve ranging from 0.771 to 0.948. In conclusion, we successfully established and conducted MS-based glycoproteomic analysis to identify novel cyst fluid glycoprotein biomarkers for PCN. These findings hold significant clinical implications, providing valuable insights for PCN decision-making, and potentially offering therapeutic targets for PCN treatment.
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页数:10
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