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Expression of p53, p16 and COX-2 in pancreatic cancer with tissue microarray
引用本文:Lei Xu,You-Ming Li,Chao-Hui Yu,Lan Li,You-Shi Liu,Bao-Feng Zhang,Jing Fang,Qiong Zhou,Ying Hu and Hen-Jun Gao Department of Gastroenterology,First Affiliated Hospital,Zhejiang University School of Medicine,Hangzhou 310003,China and National Engineering Center for Biochip,Shanghai 200000,China. Expression of p53, p16 and COX-2 in pancreatic cancer with tissue microarray[J]. Hepatobiliary & Pancreatic Diseases International, 2006, 0(1)
作者姓名:Lei Xu  You-Ming Li  Chao-Hui Yu  Lan Li  You-Shi Liu  Bao-Feng Zhang  Jing Fang  Qiong Zhou  Ying Hu and Hen-Jun Gao Department of Gastroenterology  First Affiliated Hospital  Zhejiang University School of Medicine  Hangzhou 310003  China and National Engineering Center for Biochip  Shanghai 200000  China
作者单位:Lei Xu,You-Ming Li,Chao-Hui Yu,Lan Li,You-Shi Liu,Bao-Feng Zhang,Jing Fang,Qiong Zhou,Ying Hu and Hen-Jun Gao Department of Gastroenterology,First Affiliated Hospital,Zhejiang University School of Medicine,Hangzhou 310003,China and National Engineering Center for Biochip,Shanghai 200000,China
基金项目:The study was supported by a grant from the National 863 program (2002AA2Z2021).
摘    要:BACKGROUND: Pancreatic cancer development and progression is driven by the accumulation of genetic changes. In this study we constructed tissue microarray containing specimens from pancreatic cancer, adjacent non-cancer tissue and normal tissue to survey the expression of p53, p16 and cyclooxyganase-2 (COX-2). METHODS: Tissue microarray containing 337 specimens from different stages of pancreatic cancer, adjacent noncancer tissue and normal tissues was constructed, and the expression of p53, p16 and COX-2 was assayed by immunohistochemistry to consecutive formalin-fixed tissue microarray sections. RESULTS: The expression of p53, p16 and COX-2 was significantly higher in tumorous tissues than in non-tumorons ones. A significant relationship was observed between p53 and COX-2, or p16 and COX-2. But no obvious correlation was seen between p53 and p16 expressions. Logistic regression analysis showed p53 and COX-2 as dependent predictors in pancreatic carcinogenesis, and a reciprocal relationship to neoplastic progression between p53 and COX-2. CONCLUSION: Combination analysis of p53 and COX-2 may be useful in predicting pancreatic carcinogenesis.


Expression of p53, p16 and COX-2 in pancreatic cancer with tissue microarray
Lei Xu,You-Ming Li,Chao-Hui Yu,Lan Li,You-Shi Liu,Bao-Feng Zhang,Jing Fang,Qiong Zhou,Ying Hu and Hen-Jun Gao. Expression of p53, p16 and COX-2 in pancreatic cancer with tissue microarray[J]. 国际肝胆胰疾病杂志, 2006, 0(1)
Authors:Lei Xu  You-Ming Li  Chao-Hui Yu  Lan Li  You-Shi Liu  Bao-Feng Zhang  Jing Fang  Qiong Zhou  Ying Hu  Hen-Jun Gao
Affiliation:Lei Xu,You-Ming Li,Chao-Hui Yu,Lan Li,You-Shi Liu,Bao-Feng Zhang,Jing Fang,Qiong Zhou,Ying Hu and Hen-Jun Gao Department of Gastroenterology,First Affiliated Hospital,Zhejiang University School of Medicine,Hangzhou 310003,China and National Engineering Center for Biochip,Shanghai 200000,China
Abstract:BACKGROUND: Pancreatic cancer development and progression is driven by the accumulation of genetic changes. In this study we constructed tissue microarray containing specimens from pancreatic cancer, adjacent non-cancer tissue and normal tissue to survey the expression of p53, p16 and cyclooxyganase-2 (COX-2). METHODS: Tissue microarray containing 337 specimens from different stages of pancreatic cancer, adjacent noncancer tissue and normal tissues was constructed, and the expression of p53, p16 and COX-2 was assayed by immunohistochemistry to consecutive formalin-fixed tissue microarray sections. RESULTS: The expression of p53, p16 and COX-2 was significantly higher in tumorous tissues than in non-tumorons ones. A significant relationship was observed between p53 and COX-2, or p16 and COX-2. But no obvious correlation was seen between p53 and p16 expressions. Logistic regression analysis showed p53 and COX-2 as dependent predictors in pancreatic carcinogenesis, and a reciprocal relationship to neoplastic progression between p53 and COX-2. CONCLUSION: Combination analysis of p53 and COX-2 may be useful in predicting pancreatic carcinogenesis.
Keywords:pancreatic cancer  tissue microarray  p53  p16  cyclooxygenase-2
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