南方医科大学学报
南方醫科大學學報
남방의과대학학보
JOURNAL OF SOUTHERN MEDICAL UNIVERSITY
2009年
10期
2135-2137
,共3页
杨文彬%蔡锋%程传涛%曹罡%秦兆寅
楊文彬%蔡鋒%程傳濤%曹罡%秦兆寅
양문빈%채봉%정전도%조강%진조인
胰腺癌%PSCA%组织芯片
胰腺癌%PSCA%組織芯片
이선암%PSCA%조직심편
pancreatic carcinoma%prostate stem cell antigen%tissue microarray
目的 检测PSCA在胰腺癌中的表达情况,探讨PSCA在胰腺癌发病中所起的作用.方法 用组织芯片技术构建包含78例导管腺癌,12例慢性胰腺炎患者,10例正常胰腺组织的100点阵的石蜡组织芯片.用免疫组化SP法检测该芯片中PSCA的表达,分析其与胰腺癌I临床病理因素的关系.结果 78例胰腺癌患者中,PSCA阳性表达率为79.5%(62/78),与正常组比较PSCA表达与胰腺癌显著相关(X~2=15.81,P<0.005),与慢性胰腺炎比较PSCA亦与胰腺癌显著相关(X~2=11.33,P<0.005);PSCA表达与年龄、性别、组织分化程度及TNM分期无明显相关性.结论 PSCA阳性表达与胰腺癌相关,可能与胰腺癌的发生发展有着密切关系,但与胰腺癌的临床病理特型无关.
目的 檢測PSCA在胰腺癌中的錶達情況,探討PSCA在胰腺癌髮病中所起的作用.方法 用組織芯片技術構建包含78例導管腺癌,12例慢性胰腺炎患者,10例正常胰腺組織的100點陣的石蠟組織芯片.用免疫組化SP法檢測該芯片中PSCA的錶達,分析其與胰腺癌I臨床病理因素的關繫.結果 78例胰腺癌患者中,PSCA暘性錶達率為79.5%(62/78),與正常組比較PSCA錶達與胰腺癌顯著相關(X~2=15.81,P<0.005),與慢性胰腺炎比較PSCA亦與胰腺癌顯著相關(X~2=11.33,P<0.005);PSCA錶達與年齡、性彆、組織分化程度及TNM分期無明顯相關性.結論 PSCA暘性錶達與胰腺癌相關,可能與胰腺癌的髮生髮展有著密切關繫,但與胰腺癌的臨床病理特型無關.
목적 검측PSCA재이선암중적표체정황,탐토PSCA재이선암발병중소기적작용.방법 용조직심편기술구건포함78례도관선암,12례만성이선염환자,10례정상이선조직적100점진적석사조직심편.용면역조화SP법검측해심편중PSCA적표체,분석기여이선암I림상병리인소적관계.결과 78례이선암환자중,PSCA양성표체솔위79.5%(62/78),여정상조비교PSCA표체여이선암현저상관(X~2=15.81,P<0.005),여만성이선염비교PSCA역여이선암현저상관(X~2=11.33,P<0.005);PSCA표체여년령、성별、조직분화정도급TNM분기무명현상관성.결론 PSCA양성표체여이선암상관,가능여이선암적발생발전유착밀절관계,단여이선암적림상병리특형무관.
Objective To investigate the expression of prostate stem cell antigen (PSCA) in human pancreatic carcinoma and explore its role in the oncogenesis of pancreatic cancer. Methods A pancreatic carcinoma tissue microarray was constructed, which contained 10 normal adult pancreas tissues, 12 chronic pancreatitis tissues and 78 pancreatic carcinomas. Immunohistochemistry was employed to detect the expression of PSCA, and the relation between PSCA expression and the clinicopathological factors of pancreatic carcinoma was analyzed. Results The positivity rate of PSCA in pancreatic carcinoma was 79.5 % (62/78), and PSCA staining was more intense in the malignant cells than in the benign cells (x~2=15.81, P<0.005) and chronic pancreatitis tissues (x~2=11.33, P<0.005). No obvious association was found between PSCA expression and the other variables of pancreatic carcinoma (including gender, age at surgery, tumor grade, and TNM stages). Conclusion The expression of PSCA can be related to the development of pancreatic cancer, but not to the clinicopathological factors of the tumor.