Relationship between pancreatic cancer and Maresin 1

Hakan Varol, Özlem Gül, B. Ergül, Üçler Kısa, E. Tekin, D. Oğuz
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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.
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胰腺癌与Maresin的关系
目的:胰腺癌是癌症死亡的第四大常见原因。此外,胰腺癌是胰腺最常见的原发性恶性肿瘤。胰腺癌的危险因素有很多,包括年龄、某些遗传综合征、吸烟、糖尿病、酗酒和肥胖。在我们的研究中,我们旨在评估负责炎症消退的Maresin 1 (MaR1)在胰腺癌发病机制中的作用及其在慢性胰腺炎和胰腺癌之间的差异。方法:本研究纳入47例诊断为胰腺癌的患者,32例诊断为慢性胰腺炎的患者,以及30名自2021年10月起向我诊所申请进行常规对照的无其他疾病的志愿者。利用ELISA技术从这些志愿者的血液样本中测量了MaR1水平。结果:本研究中,胰腺癌组MaR1水平为374.42 (97.27 ~ 74.129)pg/ml,慢性胰腺炎组为491.39 (252.66 ~ 949.28)pg/ml,健康对照组为558.53(286.94)。-886,68) pg/ml。胰腺癌患者组与慢性胰腺炎患者及健康对照组比较差异有统计学意义。胰腺癌患者组MaR1水平低于慢性胰腺炎患者组(p=0.01)。在我们的ROC分析中,MaR1的判别性能(AUC=0.651;(95%置信区间:0.535—-0.754);P =0.0169值)对慢性胰腺炎患者组预测胰腺癌较高。MaR1 - 315.52的截断点灵敏度为36.17%,选择性为90.62%。结论:促炎细胞因子在胰腺癌的发病机制中发挥作用,其增加是由于参与溶解途径的脂质介质的减少。MaR1的减少可能引发慢性炎症和胰腺癌的发生。MaR1在预测慢性胰腺炎患者进展为胰腺癌方面可能在临床实践中做出重要的诊断贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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