首页 | 本学科首页   官方微博 | 高级检索  
检索        

卵巢上皮性肿瘤组织中KiSS-1、基质金属蛋白酶9和核因子κBp65蛋白的表达及其相关性
作者姓名:Gao GL  Liu LD  Zou XS  Chen WX
作者单位:1. 330029,南昌,江西省肿瘤医院妇瘤科
2. 武汉市第一医院妇产科
基金项目:江西省卫生系统学术带头人计划(20045047)
摘    要:目的 探讨KiSS-1、基质金属蛋白酶9(MMP-9)、核因子κB(NF-κB)p65蛋白3者在卵巢上皮性肿瘤组织中的表达及其相关性。方法 采用免疫组化方法检测50份卵巢上皮性癌(卵巢癌)、20份卵巢交界性肿瘤、20份卵巢良性肿瘤和10份正常卵巢组织中KiSS-1、MMP-9、NF-κBp65蛋白的表达,并分析其临床意义及3者间的相关性。结果 KiSS-1蛋白在卵巢癌组织中的阳性表达率(80%)明显高于良性肿瘤组织及正常卵巢组织(分别为35%、10%;P〈0.05);在卵巢交界性肿瘤组织中阳性表达率(65%)明显高于正常卵巢组织(P〈0.05)。在卵巢癌组织中,KiSS-1蛋白阳性表达率与淋巴结转移有关(P〈0.05),与手术病理分期、病理类型及病理分级均无关(P〉0.05);MMP-9蛋白阳性表达率与手术病理分期及淋巴结转移有关(P〈0.05),而与病理类型及病理分级均无关(P〉0.05);NF-KBp65蛋白阳性表达率与手术病理分期、病理分级及淋巴结转移有关(P〈0.05),而与病理类型无关(P〉0.05)。在卵巢癌组织中,KiSS-1与MMP-9、NF.KBp65蛋白表达呈显著负相关关系(rs=-0.547,P〈0.05;rs=-0.414,P〈0.05);MMP-9与NF-κBp65蛋白表达呈显著正相关关系(rs=0.695,P〈0.05)。结论 KiSS-1基因可能对卵巢癌的转移起一定的抑制作用;KiSS-1基因可能通过抑制MMP-9、NF-κB基因,从而发挥抑制卵巢癌转移的作用。

关 键 词:卵巢肿瘤  蛋白质类  明胶酶B  NF-κB  免疫组织化学
收稿时间:2006-07-12
修稿时间:07 12 2006 12:00AM

Expression of KiSS-1, matrix metalloproteinase-9, nuclear factor-kappaBp65 in ovarian tumour
Gao GL,Liu LD,Zou XS,Chen WX.Expression of KiSS-1, matrix metalloproteinase-9, nuclear factor-kappaBp65 in ovarian tumour[J].Chinese Journal of Obstetrics and Gynecology,2007,42(1):34-38.
Authors:Gao Guo-lan  Liu Li-dan  Zou Xue-sen  Chen Wen-xue
Institution:Department of Gynecology Oncology, Jiangxi Provincial Cancer Hospital, Nanchang 330029, China
Abstract:OBJECTIVE: To investigate the expression and correlation of KiSS-1, matrix metalloproteinase-9 (MMP-9) and nuclear factor (NF)-kappaBp65 proteins in primary epithelial ovarian tumors. METHODS: Expression of KiSS-1, MMP-9, NF-kappaBp65 proteins in primary ovarian epithelial tumors (malignant n = 50, borderline tumor n = 20, benign adenoma n = 20, normal tissue n = 10) was evaluated by immunohistochemical staining. RESULTS: Expression of metastin protein in primary epithelial ovarian cancers was significantly higher than that in ovarian benign adenoma (P < 0.05) and normal tissues (P < 0.05). Expression of metastin protein in ovarian borderline tumors was significantly higher than that in normal tissues (P < 0.05). Expression of metastin protein in ovarian cancer was significantly correlated with node metastasis (P < 0.05). However, Metastin protein expression was not correlated with different histological classifications (P > 0.05), differentiation grade (P > 0.05) and International Federation of Gynecology and Obstetrics (FIGO) stage (P > 0.05). MMP-9 protein was positive in 68% (34/50) of the epithelial ovarian cancers, significantly higher than that in normal tissues (20%, 2/10; P < 0.05). NF-kappaBp65 protein was positive in 72% (36/50) of the epithelial ovarian cancers, significantly higher than that in ovarian benign adenoma (30%, 6/20; P < 0.05) and normal tissues (10%, 1/10; P < 0.05). The expression of MMP-9 protein in epithelial ovarian cancer was significantly correlated with FIGO stage (P < 0.05) and lymph node metastasis (P < 0.05). However, MMP-9 protein expression was not correlated with different histological classifications (P > 0.05) and differentiation grade (P > 0.05). The expression of NF-kappaBp65 protein in epithelial ovarian cancer was significantly correlated with FIGO stage (P < 0.05), differentiation grade (P < 0.05) and lymph node metastasis (P < 0.05). However, NF-kappaBp65 protein expression was not correlated with different histological classifications (P > 0.05). There was obviously negative correlation between KiSS-1 and MMP-9 expression in ovarian cancer (rs = -0.547, P < 0.05), as well as between KiSS-1 and NF-kappaBp65 expression in ovarian cancer (rs = -0.414, P < 0.05), while there was obviously positive correlation between MMP-9 and NF-kappaBp65 expression in ovarian cancer (rs = 0.695, P < 0.05). CONCLUSION: The results indicate that KiSS-1 plays some role in suppression of the metastasis of ovarian epithelial cancers, which may be through inhibiting the expression of MMP-9 and NF-kappaBp65.
Keywords:Ovarian neoplasms  Proteins  Gelatinase B  NF-kappa B  Immunohistochemistry
本文献已被 维普 万方数据 PubMed 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号