Wang Hong, Zhang Qiongwen, Kong Hongyu, Zeng Yunhui, Hao Meiqin, Yu Ting, Peng Jing, Xu Zhao, Chen Jingquan, Shi Huashan
State Key Laboratory of Biotherapy and Cancer Center, West China School of Medicine/West China Hospital, Sichuan University Chengdu, Sichuan Province, P.R. China.
Int J Clin Exp Pathol. 2014 Jun 15;7(7):3876-86. eCollection 2014.
A great deal of studies have been performed on the prognostic value of monocyte chemotactic protein-1 (MCP-1) in solid tumors in recent years. However, no consistent outcomes are reported. Therefore, the prognostic value of MCP-1 still remains controversial in patients with solid tumors. Here we aimed to evaluate the prognostic value of MCP-1 expression for patients with solid tumors.
Comprehensive literature was selected from PUBMED and EMBASE and clinical studies which reported analysis of survival data about MCP-1 in solid tumors were included. Stata 11.0 was used for performing a meta-analysis on evaluating the relation between MCP-1 and clinical staging, overall survival (OS) and disease free survival (DFS).
Eleven studies with a total of 1324 patients with solid tumors were included into our meta-analysis. The result showed that high concentration of MCP-1 was related to a worse OS (HR = 1.95, 95% CI 1.32-2.88). The subgroup analysis on different location of tumors showed that high concentration of MCP-1 meant bad prognosis in patients with digestive cancer (HR = 2.66, 95% CI 1.44-4.91) and urogenital cancer (HR = 2.23, 95% CI 1.61-3.10), even head and neck cancer (HR = 1.99, 95% CI 0.95-4.18) other than respiratory cancer (HR = 1.10, 95% CI 0.39-3.11). Another subgroup analysed on different sites of cancer and indicated a poor prognosis on adenocarcinoma (HR = 2.10, 95% CI 1.63-2.69).
Our findings suggest that MCP-1 can be regarded as a poor prognostic maker for solid tumors and may represent important new therapeutic targets.
近年来,针对单核细胞趋化蛋白-1(MCP-1)在实体瘤中的预后价值开展了大量研究。然而,所报道的结果并不一致。因此,MCP-1在实体瘤患者中的预后价值仍存在争议。在此,我们旨在评估MCP-1表达对实体瘤患者的预后价值。
从PUBMED和EMBASE中筛选综合文献,并纳入报道实体瘤中MCP-1生存数据分析的临床研究。使用Stata 11.0对MCP-1与临床分期、总生存期(OS)和无病生存期(DFS)之间的关系进行荟萃分析。
我们的荟萃分析纳入了11项研究,共计1324例实体瘤患者。结果显示,MCP-1高浓度与较差的OS相关(HR = 1.95,95%CI 1.32 - 2.88)。对不同肿瘤部位的亚组分析表明,MCP-1高浓度意味着消化道癌(HR = 2.66,95%CI 1.44 - 4.91)、泌尿生殖系统癌(HR = 2.23,95%CI 1.61 - 3.10)甚至头颈癌(HR = 1.99,95%CI 0.95 - 4.18)患者预后不良,而呼吸道癌患者除外(HR = 1.10,95%CI 0.39 - 3.11)。另一项对不同癌症部位的亚组分析表明,腺癌患者预后不良(HR = 2.10,95%CI 1.63 - 2.69)。
我们的研究结果表明,MCP-1可被视为实体瘤的不良预后标志物,可能代表重要的新治疗靶点。