检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:叶定伟[1] 李慧[2] Priscilla Chauvin 孙颖浩[1] 钱松溪[1] 郑家富[1] 马永江[1]
机构地区:[1]上海第二军医大学长海医院泌尿外科 [2]上海第二军医大学长海医院内分泌科,上海200433 [3]美国UTMD Anderson Cancer enter(PriscillaChauvin)
出 处:《肿瘤防治杂志》2002年第2期157-158,159,共3页China Journal of Cancer Prevention and Treatment
基 金:国家自然基金资助 ( 395 70 70 3)
摘 要:目的 :研究人前列腺癌组织中有丝分裂激活蛋白激酶 (MAPK)激活和前列腺癌发生、恶化进展的关系。方法 :采用免疫组织化学分析方法 ,用抗磷酸化MAPK蛋白的抗体检测 4 8例人前列腺癌组织标本中MAPK激活。结果 :所有前列腺癌组织中均有磷酸化MAPK蛋白表达 ,而非癌前列腺组织中未发现有磷酸化MAPK蛋白表达。磷酸化MAPK蛋白表达强阳性在Gleason分值≤ 7和 8~ 10组中分别为 2 0 %和 6 1.1% (P <0 .0 1) ;在局部浸润性肿瘤 (T3 期 )中强阳性率 5 7 1%明显高于局限性肿瘤 (T1~T2 期 ) 2 6 5 % (P <0 .0 1)。结论 :MAPK激活和人前列腺癌的发生及恶化进展密切相关 ,可以作为估价前列腺癌恶性程度和预后的指标。Objective To investigate the activation of mitogen activated protein kinase(MAPK) in prostate carcinoma tissues.Methods In 48 human prostate carcinoma specimens,the activation of MAPK was recognized by antibody specifically against phosphorylated MAPK protein by using immunohistochemistry method.Results Activation of MAPK was found in all carcinoma tissues,whereas no expression of phosphorylated MAPK protein was detected in noncarcinoma tissues.Intensive expression of phosphorylated MAPK protein was found in 11 cases with Gleason scores 8-10(61 1%) and 6 cases with Gleason score 7 or less than 20%( P <0 01).Intensive expression of phosphorylated MAPK protein in localized tumors(T 1-T 2) 57 1% is much higher than in localized invasive tumors(T 3)26 5%( P <0.01).Expression of phosphorylated MAPK protein is not associated with the level of serum prostate specific antigen.Conclusions Activation of MAPK may play a strong role in the development and progression of human prostate carcinoma.Hence,intensive expression of phosphorylated MAPK protein may be used as a tumor marker evaluating the histograde,clinical stage and prognosis.
关 键 词:有丝分裂激活蛋白激酶 激活 前列腺癌 恶化 进展
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.145