Kovacs E
Society for Cancer Research, Arlesheim, Switzerland.
Biomed Pharmacother. 2001 Sep;55(7):391-6. doi: 10.1016/s0753-3322(01)00079-8.
The serum levels of interleukin-6 (IL-6), sIL-6R and sgp130 were investigated in 76 cancer patients in comparison with 28 healthy controls. IL-6 is a multifunctional cytokine involved in certain malignant diseases. Soluble IL-6 receptor as agonist enhances the biological effect of released IL-6. Soluble gp130 as antagonist inhibits the effect of the IL-6/sIL-6R complex. Patients with different types of tumour (breast/gastrointestinal/uterine/ovarian/renal/bladder) were divided into four groups according to tumour stage and previous therapy (stage I + II without or after chemo-/radiotherapy, stage III + IV without or after chemo-/radiotherapy). The distribution of different tumour histotypes was similar in each group of patients. The levels of the three serum parameters were determined by ELISA. At each tumour stage either without or after chemo-/radiotherapy, the serum values of IL-6 were found to be not significantly different from those of controls. The values of sIL-6R were significantly elevated in stage I + II (P < 0.02) patients, with a borderline significance in stage III + IV (P = 0.06), in both cases only when no additional therapy was initiated. The serum values of sgp130 increased significantly at each tumour stage both without and after chemo-/radiotherapy (P < 0.001). A significant correlation was found between the values of sIL-6R and sgp130 in stage I + II (P < 0.02) and III + IV (P < 0.004) patients, in both cases without chemo-/radiotherapy. There were no other significant correlations. In conclusion, the simultaneous measurement of IL-6, sIL-6R and sgp130 in sera is an important factor in evaluating the biological effect of IL-6 in malignant disease. This is the first report to investigate sgp130 in cancer patients with different types of tumour.
对76例癌症患者的血清白细胞介素-6(IL-6)、可溶性IL-6受体(sIL-6R)和可溶性糖蛋白130(sgp130)水平进行了研究,并与28名健康对照者进行比较。IL-6是一种参与某些恶性疾病的多功能细胞因子。作为激动剂的可溶性IL-6受体可增强释放的IL-6的生物学效应。作为拮抗剂的可溶性gp130可抑制IL-6/sIL-6R复合物的效应。患有不同类型肿瘤(乳腺癌/胃肠道癌/子宫癌/卵巢癌/肾癌/膀胱癌)的患者根据肿瘤分期和既往治疗情况(I + II期未接受或接受过化疗/放疗,III + IV期未接受或接受过化疗/放疗)分为四组。每组患者中不同肿瘤组织学类型的分布相似。通过酶联免疫吸附测定法(ELISA)测定这三种血清参数的水平。在每个肿瘤分期,无论是否接受化疗/放疗,IL-6的血清值与对照组相比均无显著差异。sIL-6R的值在I + II期患者中显著升高(P < 0.02),在III + IV期患者中有临界显著性(P = 0.06),两种情况均仅在未开始额外治疗时出现。无论是否接受化疗/放疗,sgp130的血清值在每个肿瘤分期均显著升高(P < 0.001)。在I + II期(P < 0.02)和III + IV期(P < 0.004)患者中,在两种情况下均未接受化疗/放疗时,发现sIL-6R和sgp130的值之间存在显著相关性。没有其他显著相关性。总之,同时测定血清中的IL-6、sIL-6R和sgp130是评估IL-6在恶性疾病中生物学效应的一个重要因素。这是第一份研究不同类型肿瘤癌症患者中sgp130的报告。