Ciocan Andra, Ciocan Răzvan A, Al Hajjar Nadim, Benea Andreea M, Pandrea Stanca L, Cătană Cristina S, Drugan Cristina, Oprea Valentin C, Dîrzu Dan S, Bolboacă Sorana D
Department of Surgery-Surgery Clinic III, "Iuliu Hațieganu" University of Medicine and Pharmacy Cluj-Napoca, 400006 Cluj-Napoca, Romania.
"Prof. Dr. Octavian Fodor" Regional Institute of Gastroenterology and Hepatology Cluj-Napoca, 400006 Cluj-Napoca, Romania.
Biomedicines. 2023 Mar 14;11(3):894. doi: 10.3390/biomedicines11030894.
Chronic inflammation is demonstrated to play a direct role in carcinogenesis. Our exploratory study aimed to assess the potential added value of two inflammation biomarkers, chitotriosidase and neopterin, in follow-up evaluation of patients with colorectal cancer (CRC). An observational exploratory study was conducted. Patients with CRC and matched controls (1:1, age, sex, and living environment) were evaluated. The patients with CRC (CRC group) and controls were assessed at baseline (before surgical intervention for patients with CRC). Patients with CRC were also evaluated at 1-year follow-up. Significantly more patients with blood group A (54.5% vs. 25.0%) and smokers (50.0% vs. 22.7%) were in the CRC group. The serum values of chitotriosidase and neopterin were higher in CRC patients than in controls, but only neopterin reached the conventional level of statistical significance (-value = 0.015). The circulating chitotriosidase and neopterin values decreased significantly at 1-year follow-up (-value < 0.0001). Patients with higher N- and M-stage showed statistically significant higher levels of chitotriosidase and neopterin at baseline and 1-year follow-up (-values < 0.03). Circulating chitotriosidase levels also showed statistically significant differences regarding baseline and 1-year follow-up on patients with CRC and different differentiation grades (-values < 0.02). The circulating levels of neopterin significantly decreased at 1-year follow-up, indicating its potential as a prognostic marker. The circulating values of chitotriosidase and neopterin exhibit significant differences in patients with than without recurrences. Our results support further evaluation of chitotriosidase and neopterin as prognostic markers in patients with CRC.
慢性炎症被证明在致癌过程中起直接作用。我们的探索性研究旨在评估两种炎症生物标志物几丁质酶和新蝶呤在结直肠癌(CRC)患者随访评估中的潜在附加价值。进行了一项观察性探索性研究。对CRC患者和匹配的对照组(1:1,年龄、性别和生活环境)进行了评估。CRC患者(CRC组)和对照组在基线时(CRC患者手术干预前)进行了评估。CRC患者在1年随访时也进行了评估。CRC组中血型为A的患者(54.5%对25.0%)和吸烟者(50.0%对22.7%)明显更多。CRC患者的血清几丁质酶和新蝶呤值高于对照组,但只有新蝶呤达到了传统的统计学显著水平(P值=0.015)。循环中的几丁质酶和新蝶呤值在1年随访时显著下降(P值<0.0001)。N期和M期较高的患者在基线和1年随访时几丁质酶和新蝶呤水平在统计学上显著更高(P值<0.03)。CRC患者不同分化程度在基线和1年随访时循环几丁质酶水平也显示出统计学显著差异(P值<0.02)。新蝶呤的循环水平在1年随访时显著下降,表明其作为预后标志物的潜力。几丁质酶和新蝶呤的循环值在有复发和无复发的患者中存在显著差异。我们的结果支持进一步评估几丁质酶和新蝶呤作为CRC患者的预后标志物。