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MUC1的表达与乳腺癌细胞粘附的关系
引用本文:Lu L,Deng HY,Fan WK. MUC1的表达与乳腺癌细胞粘附的关系[J]. 癌症, 2004, 23(11): 1294-1296
作者姓名:Lu L  Deng HY  Fan WK
作者单位:浙江省杭州市第六人民医院,杭州,310014;重庆医科大学,病理生理学教研室,重庆,400016
基金项目:重庆市医学科技计划,99-2031,
摘    要:背景与目的:近年研究认为,肿瘤的转移与肿瘤细胞膜上粘液型糖蛋白的大量形成有关。本实验研究糖基化抑制剂苯甲基-α-N-乙酰半乳糖胺对粘蛋白-1(mucin1,MUC1)形成的抑制作用及其对乳腺癌细胞株MDA-MB-231细胞的粘附、侵袭转移能力的影响。方法:免疫细胞化学法检测MUC1表达,噻唑蓝比色法(MTT)检测细胞对人工基底膜(Matrigel)的粘附能力,明胶酶谱法(zymography)检测MDA-MB-231细胞MMP-2、MMP-9的分泌变化。结果:经苯甲基-α-N-乙酰半乳糖胺去糖基化处理后的肿瘤细胞组与相应对照组比较,MUC1表达降低,对基底膜的粘附力明显降低(P<0.01),同时细胞中MMP-2和MMP-9的分泌量显著下降。结论:MUC1表达水平与肿瘤细胞的粘附能力相关,MUC1的抑制使乳腺癌MDA-MB-231细胞粘附能力,分泌Ⅳ型胶原酶能力明显减弱。

关 键 词:粘蛋白 1  苯甲基-α-N-乙酰半乳糖胺  乳腺肿瘤  MDA-MB-231细胞株  粘附  侵袭转移
文章编号:1000-467X(2004)11-1294-03
修稿时间:2003-12-11

Correlation of MUC1 expression to adhesion of breast cancer cell line MDA-MB-231
Lu Li,Deng Hua-Yu,Fan Wei-Ke. Correlation of MUC1 expression to adhesion of breast cancer cell line MDA-MB-231[J]. Chinese journal of cancer, 2004, 23(11): 1294-1296
Authors:Lu Li  Deng Hua-Yu  Fan Wei-Ke
Affiliation:Department of Pathophysiology, Chongqing University of Medical Sciences, Chongqing 400 016, P.R. China.
Abstract:BACKGROUND & OBJECTIVE: Recent researches found that an abundant production of mucin protein well correlates with tumor cell metastasis. This study was to investigate inhibitory effect of benzyl-alpha-GalNAc on production of mucin 1 (MUC1), and on adhesion and invasion of breast cancer cell line MDA-MB-231. METHODS: MDA-MB-231 cells were incubated with benzyl-alpha-GalNAc, expression of MUC1 was detected by immunohistochemistry, adhesive ability of MDA-MB-231 cells to artificial basement membrane Matrigel was measured by MTT assay. Gelatin zymography was performed to detect the secretion changes of matrix metalloproteinase-2 (MMP-2) and MMP-9. RESULTS: Compared with control cells, the tumor cells deglycosylated by benzyl-alpha-GalNAc showed lower expression of MUC1 (P < 0.05), and less adhesion to the Matrigel (P< 0.01), the secretion of MMP-2 and MMP-9 suppressed (P< 0.05). CONCLUSION: The expression of MUC1 correlates to adhesion and invasion of MDA-MB-231 cells, benzyl-alpha-GalNAc may weaken adhesion and type IV collagenase-secreting activity of MDA-MB-231 cells by inhibiting MUC1.
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