Wu Kongju, Yu Shengnan, Liu Qian, Bai Xianguang, Zheng Xinhua, Wu Kongming
Medical School of Pingdingshan University, Pingdingshan, Henan.
Department of Oncology, Tongji Hospital of Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, People's Republic of China.
Onco Targets Ther. 2017 Nov 21;10:5561-5573. doi: 10.2147/OTT.S148772. eCollection 2017.
As a CXC-type chemokine, ENA78/CXCL5 is an important attractant for granulocytes by binding to its receptor CXCR2. Recent studies proved that CXCL5/CXCR2 axis plays an oncogenic role in many human cancers. However, the exact clinical significance of CXCL5 in lung cancer has not been well defined. Here, we found that the serum protein expression of CXCL5 was significantly increased in non-small cell lung cancer (NSCLC) compared with that in healthy volunteers. Immunohistochemistry staining revealed that CXCL5 protein was higher in various lung cancer tissues compared with normal tissues. Moreover, CXCL5 expression correlated with histological grade, tumor size, and TNM stage in NSCLC. Elevated CXCL5 protein abundance predicted poor overall survival in adenocarcinoma patients. Further meta-analysis demonstrated that CXCL5 mRNA expression was also positively associated with tumor stage, lymph node metastasis, and worse survival. Kaplan-Meier plot analyses indicated high CXCL5 was associated with short overall survival and progression-free survival. Together, these results indicated that CXCL5 may be a potential biomarker for NSCLC.
作为一种CXC型趋化因子,ENA78/CXCL5通过与其受体CXCR2结合,是粒细胞的重要趋化剂。最近的研究证明,CXCL5/CXCR2轴在许多人类癌症中发挥致癌作用。然而,CXCL5在肺癌中的确切临床意义尚未明确界定。在此,我们发现与健康志愿者相比,非小细胞肺癌(NSCLC)患者血清中CXCL5的蛋白表达显著增加。免疫组织化学染色显示,与正常组织相比,各种肺癌组织中CXCL5蛋白含量更高。此外,CXCL5表达与NSCLC的组织学分级、肿瘤大小和TNM分期相关。CXCL5蛋白丰度升高预示腺癌患者的总生存期较差。进一步的荟萃分析表明,CXCL5 mRNA表达也与肿瘤分期、淋巴结转移及较差的生存率呈正相关。Kaplan-Meier曲线分析表明,高CXCL5水平与较短的总生存期和无进展生存期相关。总之,这些结果表明CXCL5可能是NSCLC的潜在生物标志物。