Zheng Zaosong, Cai Yuhong, Chen Haicheng, Chen Zhiliang, Zhu Dingjun, Zhong Qiyu, Xie Wenlian
Department of Urology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.
Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Sun Yat- sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.
Front Oncol. 2019 Jan 22;8:682. doi: 10.3389/fonc.2018.00682. eCollection 2018.
The chemokine ligands and their receptors play critical roles in cancer progression and patients outcomes. We found that CXCL13 was significantly upregulated in ccRCC tissues compared with normal tissues in both The Cancer Genome Atlas (TCGA) cohort and a validated cohort of 90 pairs ccRCC tissues. Statistical analysis showed that high CXCL13 expression related to advanced disease stage and poor prognosis in ccRCC. We also revealed that serum CXCL13 levels in ccRCC patients ( = 50) were significantly higher than in healthy controls ( = 40). Receiver operating characteristic (ROC) curve revealed that tissue and serum CXCL13 expression might be a diagnostic biomarker for ccRCC with an area under curve (AUC) of 0.809 and 0.704, respectively. CXCL13 was significantly associated with its receptor, CXCR5, in ccRCC tissues, and ccRCC patients in high CXCL13 high CXCR5 expression group have a worst prognosis. Functional and mechanistic study revealed that CXCL13 promoted the proliferation and migration of ccRCC cells by binding to CXCR5 and activated PI3K/AKT/mTOR signaling pathway. These results suggested that CXCL13/CXCR5 axis played a significant role in ccRCC and might be a therapeutic target and prognostic biomarker.
趋化因子配体及其受体在癌症进展和患者预后中起着关键作用。我们发现,在癌症基因组图谱(TCGA)队列以及一个由90对ccRCC组织组成的验证队列中,与正常组织相比,CXCL13在ccRCC组织中显著上调。统计分析表明,CXCL13高表达与ccRCC的疾病晚期和不良预后相关。我们还发现,ccRCC患者(n = 50)的血清CXCL13水平显著高于健康对照(n = 40)。受试者工作特征(ROC)曲线显示,组织和血清CXCL13表达可能是ccRCC的诊断生物标志物,曲线下面积(AUC)分别为0.809和0.704。在ccRCC组织中,CXCL13与其受体CXCR5显著相关,且CXCL13高表达、CXCR5高表达组的ccRCC患者预后最差。功能和机制研究表明,CXCL13通过与CXCR5结合促进ccRCC细胞的增殖和迁移,并激活PI3K/AKT/mTOR信号通路。这些结果表明,CXCL13/CXCR5轴在ccRCC中起重要作用,可能是一个治疗靶点和预后生物标志物。