Zhu Ying-Hui, Yang Fu, Zhang Shui-Shen, Zeng Ting-Ting, Xie Xuan, Guan Xin-Yuan
State Key Laboratory of Oncology in Southern China, Sun Yat-Sen University Cancer Center Guangzhou, China.
Int J Clin Exp Pathol. 2013 Oct 15;6(11):2497-505. eCollection 2013.
Biglycan (BGN), an extracellular matrix component, has been reported to play a crucial role in the tumor progression of various cancers. However, the relation between the expression of BGN and clinical prognosis has not been studied yet. We therefore carry out the present study to elucidate the role of BGN in predicting outcomes of patients with esophageal squamous cell carcinoma (ESCC). In this study, the expression of BGN in 170 cases of ESCC tissues and matched 46 adjacent non-tumorous tissues was measured by quantitative real-time PCR and immunohistochemistry. Upregulation of BGN occurred in approximately 60% of primary ESCCs compared with their non-tumor counterparts. In addition, high expression of BGN was significantly associated with clinical stage (P = 0.009), tumor invasion (P = 0.006) and lymph node metastasis (P = 0.046). The 5-year disease-specific survival (DSS) in high expression of BGN group is poorer than that in low level expression group (36.8% VS 57.4%, P = 0.006). Stratified analysis according to the pathological stage revealed its discernibility on DSS was only pronounced in patients with advanced clinical stage (P = 0.010). Cox multivariate analysis revealed that pathologic N category (P < 0.001; hazard ratio, 2.482, 95% CI, 1.576-3.909) and BGN expression (P = 0.019; hazard ratio, 1.713, 95% CI, 1.092-2.688) were two independent prognostic factors. The findings of the present study provide evidence that BGN represents a potential novel prognostic biomarker for resected ESCC patients in advanced clinical stage.
双糖链蛋白聚糖(BGN)是一种细胞外基质成分,据报道在多种癌症的肿瘤进展中起关键作用。然而,BGN的表达与临床预后之间的关系尚未得到研究。因此,我们开展本研究以阐明BGN在预测食管鳞状细胞癌(ESCC)患者预后中的作用。在本研究中,通过定量实时PCR和免疫组织化学检测了170例ESCC组织及46例匹配的癌旁非肿瘤组织中BGN的表达。与非肿瘤对应组织相比,约60%的原发性ESCC中BGN上调。此外,BGN的高表达与临床分期(P = 0.009)、肿瘤侵袭(P = 0.006)和淋巴结转移(P = 0.046)显著相关。BGN高表达组的5年疾病特异性生存率(DSS)低于低表达组(36.8%对57.4%,P = 0.006)。根据病理分期进行的分层分析显示,其对DSS的辨别能力仅在临床晚期患者中显著(P = 0.010)。Cox多因素分析显示,病理N分期(P < 0.001;风险比,2.482,95%可信区间,1.576 - 3.909)和BGN表达(P = 0.019;风险比,1.713,95%可信区间,1.092 - 2.688)是两个独立的预后因素。本研究结果提供了证据,表明BGN是晚期临床分期的ESCC切除患者潜在的新型预后生物标志物。