Hidayat Ferdian, Labeda Ibrahim, Sampetoding Samuel, Pattelongi Ilham Jaya, Lusikooy Ronald Erasio, Dani M Iwan, Kusuma M Ihwan, Uwuratuw Julianus Aboyaman, Syarifuddin Erwin, Faruk Muhammad
Division of Digestive, Department of Surgery, Faculty of Medicine, Hasanuddin University, Makassar, Indonesia.
Faculty of Medicine, Khairun University, Ternate, Indonesia.
Ann Med Surg (Lond). 2021 Jan 23;62:334-340. doi: 10.1016/j.amsu.2021.01.013. eCollection 2021 Feb.
Tumors most often develop due to inflammatory factors, including inflammatory cells that produce cytokines and cytotoxic mediators that can stimulate malignant transformation. Knowing that interleukin-6 (IL-6) and C-reactive protein (CRP) factor into the development of colorectal cancer (CRC), we aimed to assess IL-6 and CRP's relationship with the stage and differentiation of CRC.
In a sample of 46 patients with CRC, as confirmed by histopathological examination, plasma levels of IL-6 and CRP were measured from peripheral venous blood samples before surgery and examined using enzyme-linked immunosorbent assay.
Most patients were male (63.0%) and at least 50 years old (73.9%). A positive correlation emerged between stage of CRC and both plasma IL-6 ( 0.396, .003) and CRP ( 0.376, .005) levels, which the Kruskal-Wallis test indicated were highest in stage IV (IL-6: median = 25.80, .019; CRP: median = 34.10, .040). Plasma IL-6 levels (median = 25.80, .019) were higher in well-differentiated CRC, whereas plasma CRP levels (median = 34.10, .040] were higher in poorly differentiated tissue. Linear plotting revealed a linear relationship between plasma IL-6 and plasma CRP levels in patients with CRC.
Because the stage of CRC significantly correlates with plasma IL-6 and CRP levels, IL-6 and CRP can serve as diagnostic factors in assessing the progress and prognosis of CRC.
肿瘤的发生通常归因于炎症因子,包括产生细胞因子的炎症细胞和可刺激恶性转化的细胞毒性介质。鉴于白细胞介素-6(IL-6)和C反应蛋白(CRP)在结直肠癌(CRC)的发生发展中起作用,我们旨在评估IL-6和CRP与CRC分期及分化程度的关系。
在46例经组织病理学检查确诊为CRC的患者样本中,于手术前采集外周静脉血样本,采用酶联免疫吸附测定法检测血浆IL-6和CRP水平。
大多数患者为男性(63.0%),且至少50岁(73.9%)。CRC分期与血浆IL-6(r = 0.396,P = .003)和CRP(r = 0.376,P = .005)水平呈正相关,Kruskal-Wallis检验表明IV期水平最高(IL-6:中位数 = 25.80,P = .019;CRP:中位数 = 34.10,P = .040)。高分化CRC的血浆IL-6水平(中位数 = 25.80,P = .019)较高,而低分化组织的血浆CRP水平(中位数 = 34.10,P = .040)较高。线性绘图显示CRC患者血浆IL-6和血浆CRP水平之间存在线性关系。
由于CRC分期与血浆IL-6和CRP水平显著相关,IL-6和CRP可作为评估CRC进展和预后的诊断指标。