Brindl Niall, Boekhoff Henning, Bauer Andrea S, Gaida Matthias M, Dang Hien T, Kaiser Jörg, Hoheisel Jörg D, Felix Klaus
Department of General, Visceral and Transplantation Surgery, Heidelberg University Hospital, 69120 Heidelberg, Germany.
Division of Functional Genome Analysis, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany.
Cancers (Basel). 2022 Jul 22;14(15):3562. doi: 10.3390/cancers14153562.
(1) Background: A reliable non-invasive distinction between low- and high-risk pancreatic intraductal papillary mucinous neoplasms (IPMN) is needed to effectively detect IPMN with malignant potential. This would improve preventative care and reduce the risk of developing pancreatic cancer and overtreatment. The present study aimed at exploring the presence of autoreactive antibodies in the blood of patients with IPMN of various grades of dysplasia. (2) Methods: A single-center cohort was studied composed of 378 serum samples from patients with low-grade IPMN ( = 91), high-grade IPMN ( = 66), IPMN with associated invasive cancer ( = 30), pancreatic ductal adenocarcinoma (PDAC) stages T1 ( = 24) and T2 ( = 113), and healthy controls ( = 54). A 249 full-length recombinant human protein microarray was used for profiling the serum samples. (3) Results: 14 proteins were identified as potential biomarkers for grade distinction in IPMN, yielding high specificity but mediocre sensitivity. (4) Conclusions: The identified autoantibodies are potential biomarkers that may assist in the detection of malignancy in IPMN patients.
(1) 背景:需要一种可靠的非侵入性方法来区分低风险和高风险的胰腺导管内乳头状黏液性肿瘤(IPMN),以便有效检测具有恶性潜能的IPMN。这将改善预防性护理,并降低患胰腺癌和过度治疗的风险。本研究旨在探索不同发育异常等级的IPMN患者血液中自身反应性抗体的存在情况。(2) 方法:对一个单中心队列进行研究,该队列由来自低级别IPMN患者(n = 91)、高级别IPMN患者(n = 66)、伴有浸润性癌的IPMN患者(n = 30)、胰腺导管腺癌(PDAC)T1期患者(n = 24)和T2期患者(n = 113)以及健康对照者(n = 54)的378份血清样本组成。使用一个包含249种全长重组人蛋白的微阵列对血清样本进行分析。(3) 结果:14种蛋白质被鉴定为IPMN分级区分的潜在生物标志物,具有高特异性但中等灵敏度。(4) 结论:所鉴定的自身抗体是潜在的生物标志物,可能有助于检测IPMN患者的恶性病变。