Kelly Kimberly A, Hollingsworth Michael A, Brand Randall E, Liu Christina H, Singh Vikesh K, Srivastava Sudhir, Wasan Ajay D, Yadav Dhiraj, Andersen Dana K
From the *Department of Biomedical Engineering, University of Virginia, Charlottesville, VA; †Eppley Cancer Institute, University of Nebraska School of Medicine, Omaha, NE; ‡Division of Gastroenterology, Hepatology and Nutrition, Departments of Medicine and Anesthesiology and Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, PA; §Office of Cancer Nanotechnology Research and the Division of Cancer Prevention, National Cancer Institute, National Institutes of Health, Bethesda, MD; ∥Division of Gastroenterology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD; ¶Cancer Biomarkers Research Group, Division of Cancer Prevention, National Cancer Institute, National Institutes of Health, Bethesda, MD; and #Division of Digestive Diseases and Nutrition, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD.
Pancreas. 2015 Nov;44(8):1185-94. doi: 10.1097/MPA.0000000000000552.
A workshop sponsored by the National Institute of Diabetes and Digestive and Kidney Diseases and the National Institute of Biomedical Imaging and Bioengineering focused on research gaps and opportunities in the development of new biomarkers of pancreatic disease. The session was held on July 22, 2015, and structured into 6 sessions: 1) Introduction and Overview; 2) Keynote Address; 3) New Approaches to the Diagnosis of Chronic Pancreatitis; 4) Biomarkers of Pain and Inflammation; 5) New Approaches to the Detection of Pancreatic Cancer; and 6) Shed Exosomes, Shed Cells, and Shed Proteins. Recent advances in the fields of pancreatic imaging, functional markers of pancreatic disease, proteomics, molecular and cellular imaging, and detection of circulating cancer cells and exosomes were reviewed. Knowledge gaps and research needs were highlighted. The development of new methods for the noninvasive determination of pancreatic pathology; the use of cellular markers of pancreatic function, inflammation, pain, and malignancy; and the refinement of methods to identify cells and cellular constituents of pancreatic cancer were discussed. The further refinement of sophisticated technical methods and the need for clinical studies to validate these new approaches in large-scale studies of patients at risk for the development of pancreatic disease were repeatedly emphasized.
由美国国立糖尿病、消化和肾脏疾病研究所以及国立生物医学成像和生物工程研究所主办的一次研讨会聚焦于胰腺疾病新生物标志物开发中的研究空白与机遇。该会议于2015年7月22日举行,分为6个环节:1)引言与概述;2)主题演讲;3)慢性胰腺炎诊断的新方法;4)疼痛与炎症的生物标志物;5)胰腺癌检测的新方法;6)脱落的外泌体、脱落的细胞和脱落的蛋白质。会上回顾了胰腺成像、胰腺疾病功能标志物、蛋白质组学、分子与细胞成像以及循环癌细胞和外泌体检测等领域的最新进展。突出了知识空白和研究需求。讨论了用于无创确定胰腺病理的新方法的开发;胰腺功能、炎症、疼痛和恶性肿瘤细胞标志物的使用;以及胰腺癌细胞和细胞成分识别方法的完善。反复强调了复杂技术方法的进一步完善以及开展临床研究以在胰腺疾病高危患者的大规模研究中验证这些新方法的必要性。