国家重点基础研究发展规划(973)项目(G1998051201)、国家自然科学基金(30000087和30100005)和国家自然科学基金杰出青年基金(39525022)资助.
This work was supported by grants from The Special Funds for Major State Basic Research of China (G1998051201), The National Natural Sciences Foundation of China(30000087, 30100005) and the Youth Fund of National Science Foundation of China (39525022).
为了探讨细胞周期蛋白D1(Cyclin D1)在鼻咽癌变多阶段病变组织中的蛋白质表达与鼻咽癌变的关系,应用组织微阵列(tissue microarray)技术,采用免疫组化方法检测Cyclin D1在鼻咽癌旁粘膜上皮单纯性增生/化生(simple hyperplasia/ metaplasia,SH/SM)、异型增生/化生(atypical hyperplasia/metaplasia,AH/AM)和鼻咽癌(nasopharyngeal carcinoma,NPC)的蛋白质表达,阳性表达率分别为30.0%(3/10)、90.0%(18/20)和62.9%(39/62),其中在异型增生/化生中呈“一过性增高”.表明Cyclin D1高表达可能为鼻咽癌发生过程中的早期事件;异型增生/化生可能是鼻咽癌变的重要“关卡”.
In order to investigate the relation between Cyclin D1 protein expression in multistage tissue of pathological changes during the nasopharyngeal carcinogenesis and nasopharyngeal carcinoma(NPC), the simple hyperplasia/ metaplasia, atypical hyperplasia/metaplasia in the nasopharyngeal paracarcinoma mucous epithelium and NPC were studied for Cyclin D1 expression with immunohistochemical streptavidin-peroxidase (SP) method by tissue array techenique. The positive rates were 30.0%(3/10),90.0%(18/20)and 62.9%(39/62)respectively,among which hightening “instantaneously” in the atypical hyperplasia/metaplasia appeared. It is shown high Cyclin D1 expression may be an early incident in the course of nasopharyngeal carcinogenesis, and that atypical hyperplasia/metaplasia probably be an important “toll-gate”.
宋鑫,赵晓荣,王一,周建华,关新元,曹亚.用组织微阵列技术分析鼻咽癌变多阶段组织细胞周期蛋白D1过表达[J].生物化学与生物物理进展,2002,29(3):385-389
复制生物化学与生物物理进展 ® 2024 版权所有 ICP:京ICP备05023138号-1 京公网安备 11010502031771号