High expression of IGBP1 correlates with poor prognosis in esophageal squamous cell carcinoma

被引:5
|
作者
Jiang, Sicong [1 ]
Li, Daojing [1 ]
Liang, Zibin [3 ]
Wang, Yanhua [1 ]
Pei, XiaoFeng [3 ]
Tang, Jianjun [1 ,2 ]
机构
[1] Canc Hosp Jiangxi Prov, Dept Thorac Oncol, Beijing East Rd 510, Nanchang 330006, Jiangxi, Peoples R China
[2] Nanchang Univ, Affiliated Hosp 1, Dept Resp & Crit Care Med, Nanchang, Jiangxi, Peoples R China
[3] Sun Yat Sen Univ, Affiliated Hosp 5, Ctr Canc, Dept Thorac Oncol, Zhuhai, Guangdong, Peoples R China
来源
关键词
Esophageal squamous cell carcinoma; IGBP1; prognosis; PROTEIN; METASTASIS; ALPHA-4; STRATEGIES; BIOMARKER; BINDING; CBX8;
D O I
10.1177/1724600819896374
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Immunoglobulin binding protein 1 (IGBP1) is an important signal transduction regulator that mediates various functions. However, its expression profile, role, and clinical significance in cancers are uncertain. The purpose of this study was to determine the expression profile and the prognostic significance of IGBP1 in esophageal squamous cell carcinoma (ESCC). Methods: Polymerase chain reaction assay, western blotting, and immunohistochemistry (IHC) assay were performed to examine IGBP1 expression in ESCC tissues and matched adjacent non-cancerous tissues. Moreover, IHC was used to evaluate IGBP1 expression in archived 190 paraffin-embedded ESCC specimens. Statistical analyses were applied to evaluate the prognostic value and the correlations between IGBP1 expression and the clinical parameters. Results: We found that the messenger RNA and protein levels of IGBP1 were up-regulated in the ESCC tissues compared with their adjacent non-cancerous tissues. High expression of IGBP1 in ESCC patients was positively associated with T classification (P=0.013) and vital status (P=0.03). The ESCC patients with higher IGBP1expression had a shorter survival time than those with lower IGBP1 expression. Importantly, multivariate analysis demonstrated that the expression of IGBP1 was an independent prognostic factor for ESCC (P< 0.05). Conclusions: We provide the first evidence that increased IGBP1 expression correlates with poor prognosis of ESCC, and that IGBP1 may be a tumor promoter of ESCC, which provide a promising prognostic biomarker and therapeutic target for ESCC.
引用
收藏
页码:33 / 40
页数:8
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