Lipidomic profiling of human serum enables detection of pancreatic cancer
Pancreatic cancer has the worst prognosis among all cancers. Cancer screening of body fluids may improve the survival time prognosis of patients, who are often diagnosed too late at an incurable stage. Several studies report the dysregulation of lipid metabolism in tumor cells, suggesting that chang...
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Published in | Nature communications Vol. 13; no. 1; pp. 124 - 16 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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London
Nature Publishing Group UK
10.01.2022
Nature Publishing Group Nature Portfolio |
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Abstract | Pancreatic cancer has the worst prognosis among all cancers. Cancer screening of body fluids may improve the survival time prognosis of patients, who are often diagnosed too late at an incurable stage. Several studies report the dysregulation of lipid metabolism in tumor cells, suggesting that changes in the blood lipidome may accompany tumor growth. Here we show that the comprehensive mass spectrometric determination of a wide range of serum lipids reveals statistically significant differences between pancreatic cancer patients and healthy controls, as visualized by multivariate data analysis. Three phases of biomarker discovery research (discovery, qualification, and verification) are applied for 830 samples in total, which shows the dysregulation of some very long chain sphingomyelins, ceramides, and (lyso)phosphatidylcholines. The sensitivity and specificity to diagnose pancreatic cancer are over 90%, which outperforms CA 19-9, especially at an early stage, and is comparable to established diagnostic imaging methods. Furthermore, selected lipid species indicate a potential as prognostic biomarkers.
Patients with pancreatic cancer have a poor prognosis, more research is required to identify the disease at an earlier stage. Here, the authors use lipid profiles of blood samples and show that they can distinguish patients with pancreatic cancer from healthy controls. |
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AbstractList | Pancreatic cancer has the worst prognosis among all cancers. Cancer screening of body fluids may improve the survival time prognosis of patients, who are often diagnosed too late at an incurable stage. Several studies report the dysregulation of lipid metabolism in tumor cells, suggesting that changes in the blood lipidome may accompany tumor growth. Here we show that the comprehensive mass spectrometric determination of a wide range of serum lipids reveals statistically significant differences between pancreatic cancer patients and healthy controls, as visualized by multivariate data analysis. Three phases of biomarker discovery research (discovery, qualification, and verification) are applied for 830 samples in total, which shows the dysregulation of some very long chain sphingomyelins, ceramides, and (lyso)phosphatidylcholines. The sensitivity and specificity to diagnose pancreatic cancer are over 90%, which outperforms CA 19-9, especially at an early stage, and is comparable to established diagnostic imaging methods. Furthermore, selected lipid species indicate a potential as prognostic biomarkers.Pancreatic cancer has the worst prognosis among all cancers. Cancer screening of body fluids may improve the survival time prognosis of patients, who are often diagnosed too late at an incurable stage. Several studies report the dysregulation of lipid metabolism in tumor cells, suggesting that changes in the blood lipidome may accompany tumor growth. Here we show that the comprehensive mass spectrometric determination of a wide range of serum lipids reveals statistically significant differences between pancreatic cancer patients and healthy controls, as visualized by multivariate data analysis. Three phases of biomarker discovery research (discovery, qualification, and verification) are applied for 830 samples in total, which shows the dysregulation of some very long chain sphingomyelins, ceramides, and (lyso)phosphatidylcholines. The sensitivity and specificity to diagnose pancreatic cancer are over 90%, which outperforms CA 19-9, especially at an early stage, and is comparable to established diagnostic imaging methods. Furthermore, selected lipid species indicate a potential as prognostic biomarkers. Pancreatic cancer has the worst prognosis among all cancers. Cancer screening of body fluids may improve the survival time prognosis of patients, who are often diagnosed too late at an incurable stage. Several studies report the dysregulation of lipid metabolism in tumor cells, suggesting that changes in the blood lipidome may accompany tumor growth. Here we show that the comprehensive mass spectrometric determination of a wide range of serum lipids reveals statistically significant differences between pancreatic cancer patients and healthy controls, as visualized by multivariate data analysis. Three phases of biomarker discovery research (discovery, qualification, and verification) are applied for 830 samples in total, which shows the dysregulation of some very long chain sphingomyelins, ceramides, and (lyso)phosphatidylcholines. The sensitivity and specificity to diagnose pancreatic cancer are over 90%, which outperforms CA 19-9, especially at an early stage, and is comparable to established diagnostic imaging methods. Furthermore, selected lipid species indicate a potential as prognostic biomarkers. Patients with pancreatic cancer have a poor prognosis, more research is required to identify the disease at an earlier stage. Here, the authors use lipid profiles of blood samples and show that they can distinguish patients with pancreatic cancer from healthy controls. Pancreatic cancer has the worst prognosis among all cancers. Cancer screening of body fluids may improve the survival time prognosis of patients, who are often diagnosed too late at an incurable stage. Several studies report the dysregulation of lipid metabolism in tumor cells, suggesting that changes in the blood lipidome may accompany tumor growth. Here we show that the comprehensive mass spectrometric determination of a wide range of serum lipids reveals statistically significant differences between pancreatic cancer patients and healthy controls, as visualized by multivariate data analysis. Three phases of biomarker discovery research (discovery, qualification, and verification) are applied for 830 samples in total, which shows the dysregulation of some very long chain sphingomyelins, ceramides, and (lyso)phosphatidylcholines. The sensitivity and specificity to diagnose pancreatic cancer are over 90%, which outperforms CA 19-9, especially at an early stage, and is comparable to established diagnostic imaging methods. Furthermore, selected lipid species indicate a potential as prognostic biomarkers. Pancreatic cancer has the worst prognosis among all cancers. Cancer screening of body fluids may improve the survival time prognosis of patients, who are often diagnosed too late at an incurable stage. Several studies report the dysregulation of lipid metabolism in tumor cells, suggesting that changes in the blood lipidome may accompany tumor growth. Here we show that the comprehensive mass spectrometric determination of a wide range of serum lipids reveals statistically significant differences between pancreatic cancer patients and healthy controls, as visualized by multivariate data analysis. Three phases of biomarker discovery research (discovery, qualification, and verification) are applied for 830 samples in total, which shows the dysregulation of some very long chain sphingomyelins, ceramides, and (lyso)phosphatidylcholines. The sensitivity and specificity to diagnose pancreatic cancer are over 90%, which outperforms CA 19-9, especially at an early stage, and is comparable to established diagnostic imaging methods. Furthermore, selected lipid species indicate a potential as prognostic biomarkers.Patients with pancreatic cancer have a poor prognosis, more research is required to identify the disease at an earlier stage. Here, the authors use lipid profiles of blood samples and show that they can distinguish patients with pancreatic cancer from healthy controls. Patients with pancreatic cancer have a poor prognosis, more research is required to identify the disease at an earlier stage. Here, the authors use lipid profiles of blood samples and show that they can distinguish patients with pancreatic cancer from healthy controls. |
ArticleNumber | 124 |
Author | Peterka, Ondřej Melichar, Bohuslav Wolrab, Denise Škrha, Pavel Hrnčiarová, Tereza Kuchař, Ladislav Mei, Ding Kučera, Radek Vivo-Truyols, Gabriel Wenk, Markus R. Liebisch, Gerhard Höring, Marcus Cazenave-Gassiot, Amaury Hrstka, Roman Chocholoušková, Michaela Škrha, Jan Holčapek, Michal Friedecký, David Jirásko, Robert Cífková, Eva Idkowiak, Jakub Burkhardt, Ralph Karásek, Petr Greplová, Kristína Brumarová, Radana Ahrends, Robert Novotný, Ivo |
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University of Singapore – sequence: 6 givenname: Michaela surname: Chocholoušková fullname: Chocholoušková, Michaela organization: Department of Analytical Chemistry, Faculty of Chemical Technology, University of Pardubice – sequence: 7 givenname: Ondřej surname: Peterka fullname: Peterka, Ondřej organization: Department of Analytical Chemistry, Faculty of Chemical Technology, University of Pardubice – sequence: 8 givenname: Jakub surname: Idkowiak fullname: Idkowiak, Jakub organization: Department of Analytical Chemistry, Faculty of Chemical Technology, University of Pardubice – sequence: 9 givenname: Tereza surname: Hrnčiarová fullname: Hrnčiarová, Tereza organization: Department of Analytical Chemistry, Faculty of Chemical Technology, University of Pardubice – sequence: 10 givenname: Ladislav orcidid: 0000-0003-0721-6624 surname: Kuchař fullname: Kuchař, Ladislav organization: Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University and General University Hospital in Prague – sequence: 11 givenname: Robert surname: Ahrends fullname: Ahrends, Robert organization: Department of Analytical Chemistry, University of Vienna – sequence: 12 givenname: Radana orcidid: 0000-0003-1180-6977 surname: Brumarová fullname: Brumarová, Radana organization: Palacký University Olomouc, Institute of Molecular and Translational Medicine – sequence: 13 givenname: David orcidid: 0000-0002-3448-9073 surname: Friedecký fullname: Friedecký, David organization: Palacký University Olomouc, Institute of Molecular and Translational Medicine – sequence: 14 givenname: Gabriel surname: Vivo-Truyols fullname: Vivo-Truyols, Gabriel organization: Tecnometrix – sequence: 15 givenname: Pavel surname: Škrha fullname: Škrha, Pavel organization: Third Faculty of Medicine, Charles University – sequence: 16 givenname: Jan surname: Škrha fullname: Škrha, Jan organization: 3rd Department of Internal Medicine, First Faculty of Medicine, Charles University – sequence: 17 givenname: Radek surname: Kučera fullname: Kučera, Radek organization: Department of Immunochemistry Diagnostics, University Hospital in Pilsen – sequence: 18 givenname: Bohuslav surname: Melichar fullname: Melichar, Bohuslav organization: Department of Oncology, Faculty of Medicine and Dentistry, Palacký University and University Hospital – sequence: 19 givenname: Gerhard orcidid: 0000-0003-4886-0811 surname: Liebisch fullname: Liebisch, Gerhard organization: Institute of Clinical Chemistry and Laboratory Medicine, University Hospital of Regensburg – sequence: 20 givenname: Ralph orcidid: 0000-0003-1924-1202 surname: Burkhardt fullname: Burkhardt, Ralph organization: Institute of Clinical Chemistry and Laboratory Medicine, University Hospital of Regensburg – sequence: 21 givenname: Markus R. surname: Wenk fullname: Wenk, Markus R. organization: Singapore Lipidomics Incubator (SLING), Life Sciences Institute, National University of Singapore, Department of Biochemistry, Yong Loo Lin School of Medicine, National University of Singapore – sequence: 22 givenname: Amaury orcidid: 0000-0002-3050-634X surname: Cazenave-Gassiot fullname: Cazenave-Gassiot, Amaury organization: Singapore Lipidomics Incubator (SLING), Life Sciences Institute, National University of Singapore, Department of Biochemistry, Yong Loo Lin School of Medicine, National University of Singapore – sequence: 23 givenname: Petr surname: Karásek fullname: Karásek, Petr organization: Clinic of Comprehensive Cancer Care, Masaryk Memorial Cancer Institute – sequence: 24 givenname: Ivo surname: Novotný fullname: Novotný, Ivo organization: Clinic of Comprehensive Cancer Care, Masaryk Memorial Cancer Institute – sequence: 25 givenname: Kristína surname: Greplová fullname: Greplová, Kristína organization: Faculty of Medicine, Masaryk University, Research Centre for Applied Molecular Oncology, Masaryk Memorial Cancer Institute – sequence: 26 givenname: Roman orcidid: 0000-0002-6139-2664 surname: Hrstka fullname: Hrstka, Roman organization: Research Centre for Applied Molecular Oncology, Masaryk Memorial Cancer Institute – sequence: 27 givenname: Michal orcidid: 0000-0003-3978-1249 surname: Holčapek fullname: Holčapek, Michal email: Michal.Holcapek@upce.cz organization: Department of Analytical Chemistry, Faculty of Chemical Technology, University of Pardubice |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/35013261$$D View this record in MEDLINE/PubMed |
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Snippet | Pancreatic cancer has the worst prognosis among all cancers. Cancer screening of body fluids may improve the survival time prognosis of patients, who are often... Patients with pancreatic cancer have a poor prognosis, more research is required to identify the disease at an earlier stage. Here, the authors use lipid... |
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SubjectTerms | 140/58 49 631/67/1504/1713 631/67/1857 639/638/11/296 639/638/11/872 692/53/2421 Biomarkers Biomarkers, Tumor - blood Biomarkers, Tumor - genetics Blood Body fluids CA-19-9 Antigen - blood Cancer Cancer screening Case-Control Studies Ceramides - blood Data analysis Female Humanities and Social Sciences Humans Lipid metabolism Lipid Metabolism - genetics Lipidomics - methods Lipids Lysophosphatidylcholines - blood Male Medical prognosis Medical screening multidisciplinary Multivariate Analysis Pancreatic cancer Pancreatic Neoplasms Pancreatic Neoplasms - blood Pancreatic Neoplasms - diagnosis Pancreatic Neoplasms - mortality Pancreatic Neoplasms - pathology Prognosis Proportional Hazards Models Science Science (multidisciplinary) Sensitivity and Specificity Serum lipids Spectrometry Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization Sphingomyelins - blood Statistical analysis Statistical methods Tumor cells Tumors |
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Title | Lipidomic profiling of human serum enables detection of pancreatic cancer |
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