Hakan Varol, Özlem Gül, B. Ergül, Üçler Kısa, E. Tekin, D. Oğuz
{"title":"Relationship between pancreatic cancer and Maresin 1","authors":"Hakan Varol, Özlem Gül, B. Ergül, Üçler Kısa, E. Tekin, D. Oğuz","doi":"10.51271/jchor-0006","DOIUrl":null,"url":null,"abstract":"Aims: Pancreatic cancer is the 4th most common cause of death from cancer. In addition, pancreatic cancer is the most \ncommon primary malignant tumor of the pancreas. There are many risk factors for pancreatic cancer, including age, certain \ngenetic syndromes, smoking, diabetes, alcohol abuse and obesity. In our study, we aimed to evaluate the role of Maresin 1 \n(MaR1), which is responsible for the resolution of inflammation, in the pathogenesis of pancreatic cancer and its differential \npower between chronic pancreatitis and pancreatic cancer.\nMethods: The study included 47 patients diagnosed with pancreatic cancer, 32 patients diagnosed with chronic pancreatitis, \nand 30 volunteers without any additional disease who applied to the internal medicine polyclinic for routine control, who \napplied to our clinic since October 2021 and accepted to participate in the study. MaR1 levels were measured using the ELISA technique from blood samples obtained from these volunteers.\nResults: In our study, MaR1 level was 374.42 (97.27-74.129) pg/ml in the pancreatic cancer group, 491.39 (252.66-949.28) pg/ml in the chronic pancreatitis group and 558.53 (286.94) in the healthy control group. -886,68) pg/ml was measured. There was a significant difference between the pancreatic cancer patients group and the chronic pancreatitis patients and healthy control group. In the pancreatic cancer patient group, MaR1 level was found to be lower than the chronic pancreatitis group (p=0.01). In our ROC analysis, the discriminative performance of MaR1 (AUC=0.651; [95%CI: 0.535-0.754]; p=0.0169 values) was found to be high in predicting patients with pancreatic cancer according to the patient group with chronic pancreatitis. For MaR1 ?315.52 cut-off point sensitivity was 36.17% and selectivity was 90.62%.\nConclusion: Proinflammatory cytokines, which have a role in the pathogenesis of pancreatic cancer, increase as a result \nof the decrease in lipid mediators involved in resolution pathways. Reduction of MaR1 may trigger chronic inflammation \nand pancreatic carcinogenesis. MaR1 may make an important diagnostic contribution in clinical practice in predicting the \nprogression of patients with chronic pancreatitis to pancreatic cancer.","PeriodicalId":171029,"journal":{"name":"Journal of Current Hematology & Oncology Research","volume":"46 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-05-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Current Hematology & Oncology Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.51271/jchor-0006","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Aims: Pancreatic cancer is the 4th most common cause of death from cancer. In addition, pancreatic cancer is the most
common primary malignant tumor of the pancreas. There are many risk factors for pancreatic cancer, including age, certain
genetic syndromes, smoking, diabetes, alcohol abuse and obesity. In our study, we aimed to evaluate the role of Maresin 1
(MaR1), which is responsible for the resolution of inflammation, in the pathogenesis of pancreatic cancer and its differential
power between chronic pancreatitis and pancreatic cancer.
Methods: The study included 47 patients diagnosed with pancreatic cancer, 32 patients diagnosed with chronic pancreatitis,
and 30 volunteers without any additional disease who applied to the internal medicine polyclinic for routine control, who
applied to our clinic since October 2021 and accepted to participate in the study. MaR1 levels were measured using the ELISA technique from blood samples obtained from these volunteers.
Results: In our study, MaR1 level was 374.42 (97.27-74.129) pg/ml in the pancreatic cancer group, 491.39 (252.66-949.28) pg/ml in the chronic pancreatitis group and 558.53 (286.94) in the healthy control group. -886,68) pg/ml was measured. There was a significant difference between the pancreatic cancer patients group and the chronic pancreatitis patients and healthy control group. In the pancreatic cancer patient group, MaR1 level was found to be lower than the chronic pancreatitis group (p=0.01). In our ROC analysis, the discriminative performance of MaR1 (AUC=0.651; [95%CI: 0.535-0.754]; p=0.0169 values) was found to be high in predicting patients with pancreatic cancer according to the patient group with chronic pancreatitis. For MaR1 ?315.52 cut-off point sensitivity was 36.17% and selectivity was 90.62%.
Conclusion: Proinflammatory cytokines, which have a role in the pathogenesis of pancreatic cancer, increase as a result
of the decrease in lipid mediators involved in resolution pathways. Reduction of MaR1 may trigger chronic inflammation
and pancreatic carcinogenesis. MaR1 may make an important diagnostic contribution in clinical practice in predicting the
progression of patients with chronic pancreatitis to pancreatic cancer.