摘要
目的 探讨CXC趋化因子受体2(CXCR2)在胰腺导管癌(PDAC)组织中的表达及其与临床病理及预后的相关性.方法 收集2006年1月至2008年1月南通大学附属医院和南京市鼓楼医院进行Whipple根治手术的PDAC病例161例标本及其相关的临床资料,将癌组织标本制成组织芯片,用鼠抗人CXCR2单克隆抗体,经免疫组织化学方法检测PDAC组织芯片中CXCR2蛋白表达情况,结合临床病理参数和随访资料进行统计学分析.结果 PDAC组织中CXCR2蛋白高表达54.04% (87/161),胰腺正常组织高表达率为30.77% (24/78),两者差异有统计学意义(x2=11.437,P=0.00l).CXCR2在PDAC中的高表达与出现肿瘤侵犯血管(X2=6.489,P=0.011)及TNM分期晚(X2 =6.205,P =0.013)有关,差异有统计学意义.Log-rank单因素生存分析和Kaplan-Meier生存曲线确定CXCR2高表达和患者预后差异有统计学意义(P<0.05),生存函数Cox回归多因素生存分析显示,CXCR2高表达(HR:5.514,P=0.016)是胰腺癌患者预后差的独立危险因素.结论 PDAC肿瘤组织中CXCR2高表达提示患者预后差.
Objective To explore the relationship between the expression of CXC chemokine receptor 2 (CXCR2) and the clinicopathologic features with prognosis in pancreatic ductal carcinoma (PDAC) tissues.Methods The CXCR2 expression in 161 PDAC tissues were detected with immunohistochemistry using anti-human CXCR2 antibody and tissues microarray.Results The expression of CXCR2 in PDAC tumor tissues was higher than that in normal pancreatic tissues (X2 =11.437,P =0.001).The comparison of clinicopathologic characteristics and immunohistochemistry by x2 test analysis showed that a high expression of CXCR2 in PDAC was correlated with vascular invasion (x2 =6.489,P =0.011) and late TNM stage (x2 =6.205,P =0.013).Kaplan-Meier survival and Cox regression analyses showed that a high expression of CXCR2 (HR:5.514,P =0.016) was an independent prognostic factor.Conclusion A high expression of CXCR2 denotes a poor prognosis in PDAC.
出处
《中华医学杂志》
CAS
CSCD
北大核心
2014年第48期3805-3808,共4页
National Medical Journal of China
基金
国家自然科学基金青年基金(81101615)
中国博士后基金(2012M521107)
关键词
受体
趋化因子
胰腺肿瘤
免疫组化
预后
Receptors, chemokine
Pancreatic neoplasms
Immunohistochemistry
Prognosis