胰腺导管腺癌
胰腺癌
细胞外小泡
胞外囊泡
医学
胰腺
核糖核酸
病理
内科学
细胞外
生物
腺癌
仿形(计算机编程)
癌症
计算生物学
小RNA
微泡
细胞生物学
计算机科学
生物化学
基因
操作系统
作者
Shulin Yu,Yuchen Li,Zhuan Liao,Zheng Wang,Zhen Wang,Yan Li,Ling Qian,Jingjing Zhao,Huajie Zong,Bin Kang,Wen‐Bin Zou,Kun Chen,Xianghuo He,Zhiqiang Meng,Zhen Chen,Shenglin Huang,Peng Wang
出处
期刊:Gut
[BMJ]
日期:2019-09-27
卷期号:69 (3): 540-550
被引量:169
标识
DOI:10.1136/gutjnl-2019-318860
摘要
Objective Pancreatic ductal adenocarcinoma (PDAC) is difficult to diagnose at resectable stage. Recent studies have suggested that extracellular vesicles (EVs) contain long RNAs. The aim of this study was to develop a diagnostic (d-)signature for the detection of PDAC based on EV long RNA (exLR) profiling. Design We conducted a case-control study with 501 participants, including 284 patients with PDAC, 100 patients with chronic pancreatitis (CP) and 117 healthy subjects. The exLR profile of plasma samples was analysed by exLR sequencing. The d-signature was identified using a support vector machine algorithm and a training cohort (n=188) and was validated using an internal validation cohort (n=135) and an external validation cohort (n=178). Results We developed a d-signature that comprised eight exLRs, including FGA, KRT19, HIST1H2BK, ITIH2, MARCH2, CLDN1, MAL2 and TIMP1, for PDAC detection. The d-signature showed high accuracy, with an area under the receiver operating characteristic curve (AUC) of 0.960, 0.950 and 0.936 in the training, internal validation and external validation cohort, respectively. The d-signature was able to identify resectable stage I/II cancer with an AUC of 0.949 in the combined three cohorts. In addition, the d-signature showed superior performance to carbohydrate antigen 19-9 in distinguishing PDAC from CP (AUC 0.931 vs 0.873, p=0.028). Conclusion This study is the first to characterise the plasma exLR profile in PDAC and to report an exLR signature for the detection of pancreatic cancer. This signature may improve the prognosis of patients who would have otherwise missed the curative treatment window.
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