Systemic Proteome Alterations Linked to Early Stage Pancreatic Cancer in Diabetic Patients
Background: Diabetes is a risk factor associated with pancreatic ductal adenocarcinoma (PDAC), and new adult-onset diabetes can be an early sign of pancreatic malignancy. Development of blood-based biomarkers to identify diabetic patients who warrant imaging tests for cancer detection may represent...
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doaj-fd901bef311f483bb030742d5d5e55682020-11-25T02:39:55ZengMDPI AGCancers2072-66942020-06-01121534153410.3390/cancers12061534Systemic Proteome Alterations Linked to Early Stage Pancreatic Cancer in Diabetic PatientsHong Peng0Sheng Pan1Yuanqing Yan2Randall E. Brand3Gloria M. Petersen4Suresh T. Chari5Lisa A. Lai6Jimmy K. Eng7Teresa A. Brentnall8Ru Chen9The Brown Foundation Institute of Molecular Medicine, McGovern Medical School, University of Texas Health Science Center at Houston, Houston, TX 77030, USAThe Brown Foundation Institute of Molecular Medicine, McGovern Medical School, University of Texas Health Science Center at Houston, Houston, TX 77030, USADepartment of Neurosurgery, McGovern Medical School, University of Texas Health Science Center at Houston, Houston, TX 77030, USADepartment of Medicine, University of Pittsburgh, Pittsburgh, PA 15261, USADepartment of Medicine, Mayo Clinic, Rochester, MN 55902, USADepartment of Medicine, Mayo Clinic, Rochester, MN 55902, USADivision of Gastroenterology, Department of Medicine, the University of Washington, Seattle, WA 98195, USAProteomics Resource, The University of Washington, Seattle, WA 98109, USADivision of Gastroenterology, Department of Medicine, the University of Washington, Seattle, WA 98195, USASection of Gastroenterology and Hepatology, Department of Medicine, Baylor College of Medicine, Houston, TX 77030, USABackground: Diabetes is a risk factor associated with pancreatic ductal adenocarcinoma (PDAC), and new adult-onset diabetes can be an early sign of pancreatic malignancy. Development of blood-based biomarkers to identify diabetic patients who warrant imaging tests for cancer detection may represent a realistic approach to facilitate earlier diagnosis of PDAC in a risk population. Methods: A spectral library-based proteomic platform was applied to interrogate biomarker candidates in plasma samples from clinically well-defined diabetic cohorts with and without PDAC. Random forest algorithm was used for prediction model building and receiver operating characteristic (ROC) curve analysis was applied to evaluate the prediction probability of potential biomarker panels. Results: Several biomarker panels were cross-validated in the context of detection of PDAC within a diabetic background. In combination with carbohydrate antigen 19-9 (CA19-9), the panel, which consisted of apolipoprotein A-IV (APOA4), monocyte differentiation antigen CD14 (CD14), tetranectin (CLEC3B), gelsolin (GSN), histidine-rich glycoprotein (HRG), inter-alpha-trypsin inhibitor heavy chain H3 (ITIH3), plasma kallikrein (KLKB1), leucine-rich alpha-2-glycoprotein (LRG1), pigment epithelium-derived factor (SERPINF1), plasma protease C1 inhibitor (SERPING1), and metalloproteinase inhibitor 1 (TIMP1), demonstrated an area under curve (AUC) of 0.85 and a two-fold increase in detection accuracy compared to CA19-9 alone. The study further evaluated the correlations of protein candidates and their influences on the performance of biomarker panels. Conclusions: Proteomics-based multiplex biomarker panels improved the detection accuracy for diagnosis of early stage PDAC in diabetic patients.https://www.mdpi.com/2072-6694/12/6/1534proteomicspancreatic cancerpancreatic ductal adenocarcinomadiabetesmass spectrometryplasma |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Hong Peng Sheng Pan Yuanqing Yan Randall E. Brand Gloria M. Petersen Suresh T. Chari Lisa A. Lai Jimmy K. Eng Teresa A. Brentnall Ru Chen |
spellingShingle |
Hong Peng Sheng Pan Yuanqing Yan Randall E. Brand Gloria M. Petersen Suresh T. Chari Lisa A. Lai Jimmy K. Eng Teresa A. Brentnall Ru Chen Systemic Proteome Alterations Linked to Early Stage Pancreatic Cancer in Diabetic Patients Cancers proteomics pancreatic cancer pancreatic ductal adenocarcinoma diabetes mass spectrometry plasma |
author_facet |
Hong Peng Sheng Pan Yuanqing Yan Randall E. Brand Gloria M. Petersen Suresh T. Chari Lisa A. Lai Jimmy K. Eng Teresa A. Brentnall Ru Chen |
author_sort |
Hong Peng |
title |
Systemic Proteome Alterations Linked to Early Stage Pancreatic Cancer in Diabetic Patients |
title_short |
Systemic Proteome Alterations Linked to Early Stage Pancreatic Cancer in Diabetic Patients |
title_full |
Systemic Proteome Alterations Linked to Early Stage Pancreatic Cancer in Diabetic Patients |
title_fullStr |
Systemic Proteome Alterations Linked to Early Stage Pancreatic Cancer in Diabetic Patients |
title_full_unstemmed |
Systemic Proteome Alterations Linked to Early Stage Pancreatic Cancer in Diabetic Patients |
title_sort |
systemic proteome alterations linked to early stage pancreatic cancer in diabetic patients |
publisher |
MDPI AG |
series |
Cancers |
issn |
2072-6694 |
publishDate |
2020-06-01 |
description |
Background: Diabetes is a risk factor associated with pancreatic ductal adenocarcinoma (PDAC), and new adult-onset diabetes can be an early sign of pancreatic malignancy. Development of blood-based biomarkers to identify diabetic patients who warrant imaging tests for cancer detection may represent a realistic approach to facilitate earlier diagnosis of PDAC in a risk population. Methods: A spectral library-based proteomic platform was applied to interrogate biomarker candidates in plasma samples from clinically well-defined diabetic cohorts with and without PDAC. Random forest algorithm was used for prediction model building and receiver operating characteristic (ROC) curve analysis was applied to evaluate the prediction probability of potential biomarker panels. Results: Several biomarker panels were cross-validated in the context of detection of PDAC within a diabetic background. In combination with carbohydrate antigen 19-9 (CA19-9), the panel, which consisted of apolipoprotein A-IV (APOA4), monocyte differentiation antigen CD14 (CD14), tetranectin (CLEC3B), gelsolin (GSN), histidine-rich glycoprotein (HRG), inter-alpha-trypsin inhibitor heavy chain H3 (ITIH3), plasma kallikrein (KLKB1), leucine-rich alpha-2-glycoprotein (LRG1), pigment epithelium-derived factor (SERPINF1), plasma protease C1 inhibitor (SERPING1), and metalloproteinase inhibitor 1 (TIMP1), demonstrated an area under curve (AUC) of 0.85 and a two-fold increase in detection accuracy compared to CA19-9 alone. The study further evaluated the correlations of protein candidates and their influences on the performance of biomarker panels. Conclusions: Proteomics-based multiplex biomarker panels improved the detection accuracy for diagnosis of early stage PDAC in diabetic patients. |
topic |
proteomics pancreatic cancer pancreatic ductal adenocarcinoma diabetes mass spectrometry plasma |
url |
https://www.mdpi.com/2072-6694/12/6/1534 |
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