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| 膀胱癌组织中蛋白激酶C及其抑制物活性的研究 | |
| 引用本文： | 王刚,孔垂泽,杨涛,温强,李泽良,刘同才,董旭,宗志红,于秉治. 膀胱癌组织中蛋白激酶C及其抑制物活性的研究[J]. 中华泌尿外科杂志, 2001, 22(3): 148-150 |
| 作者姓名： | 王刚 孔垂泽 杨涛 温强 李泽良 刘同才 董旭 宗志红 于秉治 |
| 作者单位： | 1. 大连市友谊医院泌尿外科 2. 中国医科大学第一临床学院泌尿外科 沈阳，110001 3. 中国医科大学基础医学院临床药理教研室 沈阳，110001 4. 中国医科大学基础医学院生化教研室 沈阳，110001 |
| 基金项目： | 卫生部科学研究基金项目资助!(98 1189) |
| 摘 要： | 目的 探讨蛋白激酶C(PKC)及其抑制物(PKCI)在膀胱移行细胞癌发生过程中的分子生物学机制。方法 采用Takai法检测20例膀胱移行细胞癌及癌周正常膀胱粘膜中PKC及其内源性抑制物(PKCI)的活性。结果 膀胱癌与癌周正常膀胱粘膜相比，胞膜（8.67±2.07，10.66±1.24）、胞浆（7.68±3.27，20.63±12.77）及总体（7.71±4.52，14.34±7.47）PKC活性(pmol |
| 关 键 词： | 膀胱肿瘤 移行细胞癌 组织蛋白 膀胱癌 蛋白激酶C |
| 修稿时间： | 2000-01-31 |
Study on enzymatic activity of PKC and PKCI in the tissues of bladder carcinoma |
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| WANG Gang,KONG Chuize,YANG Tao,et al.. Study on enzymatic activity of PKC and PKCI in the tissues of bladder carcinoma[J]. Chinese Journal of Urology, 2001, 22(3): 148-150 | |
| Authors: | WANG Gang KONG Chuize YANG Tao et al. |
| Affiliation: | WANG Gang,KONG Chuize,YANG Tao,et al.Department of Urology,The First Clinical College,China Medical University,Shenyang 116001,China |
| Abstract: | Objective To study the molecule biological mechanism of PKC and PKC inhibitor (PKCI) on the carcinogenesis of bladder transitional cell carcinoma. Methods Takai method was followed to measure the activity of PKC and PKCI in 20 cases of bladder transitional cell carcinoma and in normal tissues around the tumor. Results Compared with that of the normal tissues around the tumor, PKC activity in carcinoma was reduced in the plasmic, membranous fraction and total tissue ( P <0.05);the ratio of membrane/plasm being increased significantly ( P <0.01). In addition, compared with that of the normal tissues around the tumor, PKCI activity in carcinoma increased in the plasmic and membranous fraction ( P <0.05)and increased significantly in total tissue ( P <0.01).Hence the ratio of membrane/plasm did not alter obviously ( P >0.05). Conclusions The activity of PKC and PKCI in sub cell level might play an important regulatory role in bladder carcinogenesis. PKC was activited in bladder carcinoma in a down regulation manner. |
| Keywords: | Bladder neoplasms Transitional cell carcinoma Cathepsins |
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