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CXCL17和CXCR8表达在结肠癌患者中的预后价值。

Prognostic value of CXCL17 and CXCR8 expression in patients with colon cancer.

作者信息

Yao Hongyan, Lv Yufeng, Bai Xuefeng, Yu Zhaojin, Liu Xiaojian

机构信息

Department of Pharmacology, School of Basic Medical Sciences, Jinzhou Medical University, Jinzhou, Liaoning 121001, P.R. China.

Nuclear Medicine Department, Jinzhou Central Hospital, Jinzhou, Liaoning 121001, P.R. China.

出版信息

Oncol Lett. 2020 Sep;20(3):2711-2720. doi: 10.3892/ol.2020.11819. Epub 2020 Jul 7.

Abstract

C-X-C motif chemokine ligand 17 (CXCL17) is a mucous chemokine and its expression is highly correlated with that of G protein-coupled receptor 35 (GPR35), which has been confirmed as its receptor and named C-X-C motif chemokine receptor 8 (CXCR8). CXCL17 is upregulated in several types of cancer. However, the biological role of this chemokine in colon cancer remains unknown. In the present study, the expression levels of CXCL17 and CXCR8 were examined using immunohistochemistry in 101 colon cancer tissues and 79 healthy tumour-adjacent tissues. CXCL17 and CXCR8 expression levels were increased in the colon cancer samples compared with tumour-adjacent samples. Patients with high CXCL17 expression had longer overall survival (OS) compared with patients with low expression of CXCL17 (log-rank test; P=0.027). However, CXCR8 expression, but not CXCL17, was an independent prognostic factor for OS in patients with colon cancer. The expression of CXCR8 correlated positively with that of CXCL17 in colon cancer samples (ρ=0.295; P=0.003). Furthermore, the combined high expression of CXCL17 and CXCR8 was a significant independent prognostic factor for OS in patients with colon cancer (P=0.001). In subgroups with a TNM stage of I-II, the patients with combined high expression of CXCL17 and CXCR8 had a longer survival compared with those without combined high expression (P=0.001). However, this difference was not observed in subgroups with a TNM stage of III-IV. Collectively, these findings suggest that CXCL17/CXCR8 signalling may be involved in colon cancer and contribute to improved patient outcomes.

摘要

C-X-C基序趋化因子配体17(CXCL17)是一种黏液趋化因子,其表达与G蛋白偶联受体35(GPR35)高度相关,GPR35已被确认为其受体并命名为C-X-C基序趋化因子受体8(CXCR8)。CXCL17在多种癌症类型中上调。然而,这种趋化因子在结肠癌中的生物学作用仍不清楚。在本研究中,采用免疫组织化学方法检测了101例结肠癌组织和79例健康肿瘤旁组织中CXCL17和CXCR8的表达水平。与肿瘤旁样本相比,结肠癌样本中CXCL17和CXCR8的表达水平升高。CXCL17高表达患者的总生存期(OS)长于CXCL17低表达患者(对数秩检验;P=0.027)。然而,CXCR8表达而非CXCL17表达是结肠癌患者OS的独立预后因素。在结肠癌样本中,CXCR8的表达与CXCL17的表达呈正相关(ρ=0.295;P=0.003)。此外,CXCL17和CXCR8的联合高表达是结肠癌患者OS的显著独立预后因素(P=0.001)。在TNM分期为I-II的亚组中,CXCL17和CXCR8联合高表达的患者比未联合高表达的患者生存期更长(P=0.001)。然而,在TNM分期为III-IV的亚组中未观察到这种差异。总体而言,这些发现表明CXCL17/CXCR8信号通路可能参与结肠癌并有助于改善患者预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4001/7400977/c0d97db9db93/ol-20-03-2711-g00.jpg

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