Oncotarget, Vol. 7, No. 19

www.impactjournals.com/oncotarget/

Sp1 and COX2 expression is positively correlated with a poor prognosis in pancreatic ductal adenocarcinoma Junjie Hang1,2,*, Hai Hu1,2,*, Junjie Huang3,*, Ting Han1,2, Meng Zhuo1,2, Yangyang Zhou4, Lei Wang5, Yi Wang1,2, Feng Jiao1,2, Liwei Wang1,2 1

 epartment of Medical Oncology and Pancreatic Cancer Center, Shanghai General Hospital, Shanghai Jiao Tong University D School of Medicine, Shanghai 201620, China

2

Shanghai Key Laboratory of Pancreatic Disease, Shanghai 201620, China

3

Department of Hematology, First Affiliated Hospital of Shenzhen University, Shenzhen 513000, China

4

Department of Medical Oncology, First Affiliated Hospital of Bengbu Medical College, Anhui 233004, China

5

Department of Radiation Oncology, Lianyungang First People’s Hospital, Jiangsu 222002, China

*

These authors contributed equally to this work

Correspondence to: Feng Jiao, email: [email protected] Liwei Wang, email: [email protected] Keywords: pancreatic ductal adenocarcinoma, specificity protein 1, cyclooxygenase-2, correlation, prognosis Received: January 17, 2016     Accepted: March 28, 2016     Published: April 5, 2016

ABSTRACT Previous studies showed that celecoxib, a cyclooxygenase-2 (COX2) inhibitor, can inhibit angiogenesis and metastasis of pancreatic ductal adenocarcinoma (PDAC) via the suppression of specificity protein 1 (Sp1). In this study, we investigated the prognostic value of Sp1 and COX2 in 88 PDAC patients. Our study showed there was a positive correlation between Sp1 and COX2 expression (P=0.001) by using the Spearman’s rank test. Pearson Chi-square test revealed that Sp1 and COX2 expression were positively associated with lymph node metastasis (P

Sp1 and COX2 expression is positively correlated with a poor prognosis in pancreatic ductal adenocarcinoma.

Previous studies showed that celecoxib, a cyclooxygenase-2 (COX2) inhibitor, can inhibit angiogenesis and metastasis of pancreatic ductal adenocarcino...
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