Elevated expression of CTHRC1 predicts unfavorable prognosis in patients with pancreatic ductal adenocarcinoma

被引:1
作者
Liu, Wei [1 ]
Fu, Xue-Liang [1 ]
Yang, Jian-Yu [1 ]
Yang, Min-Wei [1 ]
Tao, Ling-Ye [1 ]
Liu, De-Jun [1 ]
Huo, Yan-Miao [1 ]
Zhang, Jun-Feng [1 ]
Hua, Rong [1 ]
Sun, Yong-Wei [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Ren Ji Hosp, Dept Biliary Pancreat Surg, 160 Pujian Rd, Shanghai 200127, Peoples R China
来源
AMERICAN JOURNAL OF CANCER RESEARCH | 2016年 / 6卷 / 08期
关键词
Pancreatic ductal adenocarcinoma; CTHRC1; prognosis; biomarker; TRIPLE-HELIX REPEAT; COLORECTAL-CANCER; OVEREXPRESSION; BIOMARKERS; CARCINOMA; ADHESION; LIVER;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Collagen triple helix repeat containing-1 (CTHRC1), a secreted protein, has been demonstrated as an oncogene in many types of human cancers including pancreatic ductal adenocarcinoma (PDAC). However, little is known about the prognostic value of CTHRC1 in PDAC. In current study, we investigated the expression pattern and underlying clinical significance of CTHRC1 in PDAC. Data from public PDAC microarray datasets, real-time PCR and immunohistochemistry demonstrated that CTHRC1 expression was dramatically increased in PDAC compared with normal tissues at both mRNA and protein level, which was consistent with previous studies. Analysis of its correlation with clinicopathological parameters indicated that high protein expression level of CTHRC1 was significantly associated with lymph node metastasis, vascular invasion and perineural invasion. Kaplan-Meier survival analysis showed that patients with higher CTHRC1 expression exhibited a remarkably shorter overall survival in four different PDAC patient cohorts. Importantly, univariable and multivariable Cox regression analysis revealed that CTHRC1 protein expression level was a significant and independent prognostic factor for overall survival rate of PDAC patients. Together, these data suggested that CTHRC1 is an unfavorable biomarker of prognosis in PDAC and may serve as a potential therapeutic candidate for PDAC treatment.
引用
收藏
页码:1820 / 1827
页数:8
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