Li Ruochen, Zhang Heng, Liu Hao, Lin Chao, Cao Yifan, Zhang Weijuan, Shen Zhenbin, Xu Jiejie
Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Fudan University, Shanghai, China.
Department of General Surgery, Zhongshan Hospital, Fudan University, Shanghai, China.
Oncotarget. 2016 Apr 26;7(17):23909-18. doi: 10.18632/oncotarget.8069.
Being a critical chemokine receptor in chemoattracting myeloid cells into tumor tissues, C-C chemokine receptor 2 (CCR2) has been detected in many malignant tumors. This study aims to evaluate the prognostic value of CCR2 expression in patients with gastric cancer after surgery.
CCR2 expression was detected in the accessory cells around gastric cancer cells in a diffused manner. CCR2 high expression was correlated with tumor invasion depth (P=0.006 and P=0.004, respectively), lymph node metastasis (P=0.038 and P=0.011, respectively) and TNM stage (P=0.003 and P=0.001, respectively) in the two independent sets. Multivariate Cox regression analysis identifies CCR2 high expression was an independent poor prognostic factor for OS of patients with gastric cancer in the two sets (P=0.013 and P=0.006, respectively). Integration of CCR2 expression and TNM stage could provide additional prognostic value for OS than TNM stage alone in the two sets (P=0.038 and P=0.002, respectively).
Two independent sets comprising a total of 474 patients who received standard gastrectomy were enrolled in the study. The expression level of CCR2 was detected by immunohistochemistry. The correlations between CCR2 expression and clinicopathological factors were explored, and the prognostic significance for overall survival (OS) was determined by Kaplan-Meier analysis.
CCR2 high expression in the tumor microenvironment is a novel independent unfavorable prognostic factor for patients with gastric cancer. Combination of CCR2 expression and TNM stage could provide a better prognostic model for OS of gastric cancer patients.
C-C趋化因子受体2(CCR2)作为一种关键的趋化因子受体,可将髓样细胞吸引至肿瘤组织中,已在多种恶性肿瘤中被检测到。本研究旨在评估CCR2表达对胃癌患者术后的预后价值。
CCR2表达以弥漫方式在胃癌细胞周围的辅助细胞中被检测到。在两个独立队列中,CCR2高表达分别与肿瘤浸润深度(P分别为0.006和0.004)、淋巴结转移(P分别为0.038和0.011)及TNM分期(P分别为0.003和0.001)相关。多因素Cox回归分析表明,在两个队列中CCR2高表达是胃癌患者总生存期的独立不良预后因素(P分别为0.013和0.006)。在两个队列中,将CCR2表达与TNM分期相结合,相比于单独的TNM分期,可为总生存期提供额外的预后价值(P分别为0.038和0.002)。
本研究纳入了两个独立队列,共474例接受标准胃切除术的患者。采用免疫组织化学法检测CCR2的表达水平。探讨CCR2表达与临床病理因素之间的相关性,并通过Kaplan-Meier分析确定其对总生存期(OS)的预后意义。
肿瘤微环境中CCR2高表达是胃癌患者新的独立不良预后因素。CCR2表达与TNM分期相结合可为胃癌患者的总生存期提供更好的预后模型。