Combined Evaluation of Expression of CXCR4 and Nrf2 as Prognostic Factor for Patients with Gastric Carcinoma

被引:12
作者
Yu, Shuo [1 ,2 ]
Wu, Tao [2 ]
Wang, Jia [3 ]
Cheng, Chuantao [2 ]
Wang, Jing [4 ]
Sun, Liangzhang [5 ]
Liu, Chao [6 ]
Cao, Gang [2 ]
Hu, Tinghua [1 ]
机构
[1] Xi An Jiao Tong Univ, Affiliated Hosp 1, Dept Resp & Crit Care Med, 277 Yanta West Rd, Xian 710061, Shaanxi, Peoples R China
[2] Xi An Jiao Tong Univ, Affiliated Hosp 2, Dept Gen Surg, 157 Xiwu Rd, Xian 710000, Shaanxi, Peoples R China
[3] Xi An Jiao Tong Univ, Affiliated Hosp 1, Dept Neurosurg, Xian, Shaanxi, Peoples R China
[4] Xi An Jiao Tong Univ, Affiliated Hosp 1, Dept Oncol, Xian, Shaanxi, Peoples R China
[5] Xi An Jiao Tong Univ, Affiliated Hosp 2, Dept Thorac Surg, Xian, Shaanxi, Peoples R China
[6] Xi An Jiao Tong Univ, Affiliated Hosp 1, Dept Nephrol, Xian, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
CXCR4; Nrf2; gastric carcinoma; clinicopathological; biomarker; prognostic; CLINICOPATHOLOGICAL SIGNIFICANCE; CANCER CHEMOPREVENTION; RECEPTOR CXCR4; ACTIVATION; CHEMOKINE; OVEREXPRESSION; PROGRESSION; MECHANISMS; SURVIVAL; ROLES;
D O I
10.2174/1871520617666171103112019
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: CXC Chemokine Receptor 4 (CXCR4) and NFE-related factor 2 (Nrf2) have been observed implicated with cell malignant behavior of human cancers. Aims: In this study, we detected their expression in gastric carcinoma (GC) tissue specimens and related the result with clinicopathological data and patient survival. Methods: 120 GC and compared normal tissue specimens were processed to analyse the expression of CXCR4 and Nrf2. We found that the expression of CXCR4 and Nrf2 was dramatically increased in GC tissues when compared to the distant non-cancer tissues (P<0.05). CXCR4 overexpression was associated with the depth of invasion (P=0.006) Histological grade (P=0.018) TNMstage (P=0.021) lymph node metastasis (P<0.001)and distant metastasis (P=0.026), whereas overexpression of Nrf2 protein was significantly associated with tumor size (P=0.045), Histological grade (P=0.026), TNMstage (P=0.020), lymph node metastases (P<0.001)and distant metastasis (P=0.008). Furthermore, we observed a significant co-expression of CXCR4 and Nrf2 expression in GC specimens. Results: In the survival part, we found that GC patients with CXCR4+ and Nrf2+ had worse outcomes. The significant prognostic indicators are age, tumor size, histological grade, TNMstage, CXCR4, Nrf2, and co-expression of CXCR4 and Nrf2 in GC patients. Multivariate analysis showed that TNMstage and CXCR4+/Nrf2+ expression were risk factors. Above all we come to the conclusion that the expression of CXCR4 might partly be regulated by the level of Nrf2 and both positive expressions suggest poor prognosis of GC patients.
引用
收藏
页码:388 / 393
页数:6
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