Institute of Physiological Chemistry, Martin Luther University of Halle-Wittenberg, Halle, Germany.
Int J Cancer. 2014 Nov 1;135(9):2096-106. doi: 10.1002/ijc.28867. Epub 2014 Apr 4.
Chemokines are involved in both the negative and positive regulation of inflammatory processes, angiogenesis and cancer/cancer stem cell proliferation as well as the chemoattraction of tumor cells to metastatic sites. The aim of this study was to measure the mRNA expression levels of three chemokines, CCL2, CCL7 and CX3CL1, in soft tissue sarcomas (STSs) and to assess the correlations between these levels as well as their correlations with clinicopathological data and the disease-specific survival of STS patients. The mRNA levels of CCL2, CCL7 and CX3CL1 were analyzed in tumor tissues from 126 STS patients using qPCR. Low mRNA expression of CCL2 and CX3CL1 was significantly correlated with a worse prognosis (RR = 1.98; p = 0.019 and RR = 2.10; p = 0.014; multivariate Cox's regression analysis). A combined low expression of CCL2 and CX3CL1 was associated with a significantly increased risk of tumor-related death as compared to patients with high expression levels of both chemokines (RR = 3.08; p = 0.003). A gender-specific multivariate analysis revealed that female STS patients with low CX3CL1 mRNA expression had a 3.46-fold increased risk of death (p = 0.004). Low expression of both CCL2 and CX3CL1 mRNAs resulted in an additive 5.37-fold increased risk of tumor-related death (p = 0.003) as compared to those with high expression of both parameters in female patients. In conclusion, this is the first study to show a significant correlation between combined low expression of CCL2 and CX3CL1 and a poor prognosis for STS patients, particularly in female patients.
趋化因子参与炎症过程、血管生成和癌症/癌症干细胞增殖的负向和正向调节,以及肿瘤细胞向转移部位的趋化作用。本研究的目的是测量软组织肉瘤(STS)中三种趋化因子 CCL2、CCL7 和 CX3CL1 的 mRNA 表达水平,并评估这些水平之间的相关性及其与临床病理数据和 STS 患者的疾病特异性生存之间的相关性。使用 qPCR 分析了 126 名 STS 患者肿瘤组织中 CCL2、CCL7 和 CX3CL1 的 mRNA 水平。CCL2 和 CX3CL1 的低 mRNA 表达与预后较差显著相关(RR=1.98;p=0.019 和 RR=2.10;p=0.014;多变量 Cox 回归分析)。与两种趋化因子高表达的患者相比,CCL2 和 CX3CL1 联合低表达与肿瘤相关死亡的风险显著增加相关(RR=3.08;p=0.003)。性别特异性多变量分析显示,低 CX3CL1 mRNA 表达的女性 STS 患者死亡风险增加 3.46 倍(p=0.004)。与两种参数高表达的女性患者相比,CCL2 和 CX3CL1 的低表达导致肿瘤相关死亡的风险增加了 5.37 倍(p=0.003)。总之,这是第一项表明 CCL2 和 CX3CL1 联合低表达与 STS 患者预后不良显著相关的研究,尤其是在女性患者中。