Li Guanghua, Xu Jianbo, Wang Zhao, Yuan Yujie, Li Yin, Cai Shirong, He Yulong
Department of Gastrointestinal Surgery, First Affiliated Hospital of Sun Yat-sen University, No. 58, Zhongshan 2nd Street, Guangzhou, 510080, Guangdong Province, People's Republic of China.
J Cancer Res Clin Oncol. 2015 Mar;141(3):443-52. doi: 10.1007/s00432-014-1838-5. Epub 2014 Sep 28.
Inflammation plays an important role in gastric cancer (GC) development and progression. Suppressor of cytokine signaling (SOCS)-1 and SOCS-3 negatively regulate proinflammatory cytokine signaling; however, their prognostic significance in GC remains unknown. We evaluated the clinicopathological correlation and prognostic significance of SOCS-1 and SOCS-3 in GC.
SOCS-1 and SOCS-3 mRNA levels were analyzed in 80 paired gastric tumor and adjacent normal mucosal tissues using a microarray dataset from the Gene Expression Omnibus. Univariate and multivariate analyses were performed to investigate the prognostic impact of SOCS-1 and SOCS-3 immunohistochemical expression on overall survival (OS) and relapse-free survival (RFS) in 186 consecutive GC patients who underwent curative surgery.
SOCS-1 and SOCS-3 mRNA expression levels were lower in gastric tumor tissues than in matched normal mucosa. OS and RFS were significantly longer in the high SOCS-1 and SOCS-3 expression groups than in their corresponding low expression groups (p < 0.05). High simultaneous SOCS-1 and SOCS-3 expression were associated with longer OS compared with low simultaneous SOCS-1 and SOCS-3 expression (68.8 vs. 22.2 months; p < 0.001). SOCS-1 [hazards ratio (HR) 0.54, 95 % confidence interval (CI) 0.33-0.87, p = 0.011] and SOCS-3 (HR 0.46, 95 % CI 0.26-0.80, p = 0.006) were independent prognostic factors for OS. Only SOCS-1 (HR 0.20, 95 % CI 0.11-0.38, p = 0.006) was an independent prognostic factor for RFS.
Low SOCS-1 and SOCS-3 expression are poor prognostic indicators in GC. GC patients with low SOCS-1 and SOCS-3 expression need close follow-up.
炎症在胃癌(GC)的发生和发展中起重要作用。细胞因子信号转导抑制因子(SOCS)-1和SOCS-3对促炎细胞因子信号传导起负向调节作用;然而,它们在GC中的预后意义尚不清楚。我们评估了SOCS-1和SOCS-3在GC中的临床病理相关性及预后意义。
使用来自基因表达综合数据库的微阵列数据集,分析了80对胃肿瘤及相邻正常黏膜组织中SOCS-1和SOCS-3的mRNA水平。对186例接受根治性手术的连续性GC患者,进行单因素和多因素分析,以研究SOCS-1和SOCS-3免疫组化表达对总生存期(OS)和无复发生存期(RFS)的预后影响。
胃肿瘤组织中SOCS-1和SOCS-3的mRNA表达水平低于匹配的正常黏膜。高SOCS-1和SOCS-3表达组的OS和RFS显著长于相应的低表达组(p < 0.05)。与低同时表达SOCS-1和SOCS-3相比,高同时表达SOCS-1和SOCS-3与更长的OS相关(68.8对22.2个月;p < 0.001)。SOCS-1[风险比(HR)0.54,95%置信区间(CI)0.33 - 0.87,p = 0.011]和SOCS-3(HR 0.46,95% CI 0.26 - 0.80,p = 0.006)是OS的独立预后因素。仅SOCS-1(HR 0.20,95% CI 0.11 - 0.38,p = 0.006)是RFS的独立预后因素。
低SOCS-1和SOCS-3表达是GC的不良预后指标。SOCS-1和SOCS-3低表达的GC患者需要密切随访。