Dimberg Jan, Skarstedt Marita, Löfgren Sture, Zar Niklas, Matussek Andreas
Department of Natural Science and Biomedicine, University College of Health Sciences, Jönköping, Småland SE-55111, Ryhov County Hospital, Jönköping, Småland SE-55185, Sweden.
Department of Clinical Microbiology, Ryhov County Hospital, Jönköping, Småland SE-55185, Sweden.
Biomed Rep. 2014 May;2(3):340-343. doi: 10.3892/br.2014.255. Epub 2014 Mar 17.
Chemokines (chemotactic cytokines) promote leukocyte attraction to sites of inflammation and cancer. Certain chemokines promote and regulate neoplastic progression, including metastasis and angiogenesis. One such chemokine, CXCL10, was found to be expressed in colorectal cancer (CRC) tissue. To gain insight into the prognostic significance of CXCL10, we investigated whether the levels of this chemokine were altered in the colorectal tissue or plasma of CRC patients. Using Luminex technology for protein analyses, we observed a significantly higher CXCL10 protein level in cancer tissue compared to that in paired normal tissue. Moreover, significantly higher plasma levels of CXCL10 were detected in patients compared to those in control subjects and the plasma levels of CXCL10 in disseminated disease were found to be significantly higher compared to those in localized disease. The single-nucleotide polymorphism rs8878, which has been described in exon 4 in the 3'-untranslated region of the CXCL10 gene, was investigated using a TaqMan system. There were significant differences in genotype distribution and allelic frequencies between CRC patients and control subjects. In conclusion, altered CXCL10 protein concentrations in CRC tissues or plasma and the rs8878 genotype variant of CXCL10 may contribute to the prediction of clinical outcome.
趋化因子(趋化性细胞因子)可促进白细胞向炎症和癌症部位聚集。某些趋化因子可促进和调节肿瘤进展,包括转移和血管生成。其中一种趋化因子CXCL10,被发现存在于结直肠癌(CRC)组织中。为深入了解CXCL10的预后意义,我们研究了CRC患者的结直肠组织或血浆中该趋化因子的水平是否发生改变。通过Luminex技术进行蛋白质分析,我们观察到癌组织中CXCL10蛋白水平显著高于配对的正常组织。此外,与对照组相比,患者血浆中CXCL10水平显著更高,且发现播散性疾病患者的血浆CXCL10水平显著高于局限性疾病患者。使用TaqMan系统研究了CXCL10基因3'非翻译区第4外显子中描述的单核苷酸多态性rs8878。CRC患者与对照组在基因型分布和等位基因频率上存在显著差异。总之,CRC组织或血浆中CXCL10蛋白浓度的改变以及CXCL10的rs8878基因型变异可能有助于预测临床结果。