基础医学与临床 ›› 2009, Vol. 29 ›› Issue (2): 170-173.

• 研究论文 • 上一篇    下一篇

人乳腺癌中p-p38信号分子与uPA表达增强

韩艳春 刘鲁英 杨东霞 王桂华   

  1. 滨州医学院
  • 收稿日期:2008-01-21 修回日期:2008-04-29 出版日期:2009-02-25 发布日期:2009-02-25
  • 通讯作者: 韩艳春

Increase of p-p38 and uPA expression in human breast cancer

Yan-chun HAN, Lu-ying LIU, Dong-xia YANG, Gui-hua WANG   

  1. Binzhou Medical College
  • Received:2008-01-21 Revised:2008-04-29 Online:2009-02-25 Published:2009-02-25
  • Contact: Yan-chun HAN,

摘要: 目的 研究磷酸化p38(p-p38)信号分子和uPA在乳腺癌组织及细胞中表达及意义。方法 免疫组化检测60例乳腺癌组织及其邻近正常乳腺组织中p-p38和uPA蛋白,Western blot检测人乳腺癌细胞中p-p38及uPA蛋白表达及用p38MAPK特异性抑制剂SB203580阻断p38MAPK信号通路后uPA蛋白水平的变化。结果 免疫组化显示,p-p38,uPA蛋白在乳腺癌组织中表达阳性率分别为56.7%和60.0%。,显著高于正常乳腺组织中的表达(P<0.05),并与乳腺癌的TNM分期及淋巴结转移相关(P<0.05),而与患者年龄、肿瘤大小无明显相关性,且两者表达存在正相关(r=0.316, P<0.05)。乳腺癌高转移性的MDA-MB-231细胞株p-p38及uPA蛋白表达水平高于低转移的MCF-7细胞株。 用SB203580阻断p38MAPK通路可降低uPA蛋白表达。结论 p-p38和uPA表达在乳腺癌恶性进展中起重要作用,可为乳腺癌转移机制研究提供有效线索。

关键词: p-p38, uPA, 乳腺癌

Abstract: Objective To study the expression and significance of phosphorylated p38 (p-p38) and uPA in breast cancer tissues and cells. Methods Immunohistochemistry (S-P) was used to test the protein expression of p-p38 and uPA in 60 specimens excised during operation from 50 patients with breast cancer. Western blotting was adopted to detect the protein expression of p-p38 and uPA in breast cancer cells and uPA protein expression after SB203580, an specific inhibitor of p38 MAPK blocked p38MAPK signaling pathway. Results The positive rate of p-p38 protein and uPA protein in breast cancer tissues was 56.7%and 60.0%,respectively. The protein expression levels of p-p38 and uPA in breast cancer tissues were significantly higher than those in the adjacent normal tissues(P<0.05) The protein expression of p-p38 was linearly correlated with uPA expression(r=0.316, P<0.05). The expression of p-p38 and uPA was related to lymph node metastasis and TNM stage (P<0.05), and it was not related to patients'age and tumor size. The protein expression levels of p-p38 and uPA in breast cancer cells MDA-MB-231 were higher than that in MCF-7. SB203580 nhibited p38MAPK pathway and down-regulated uPA protein expression. Conclusion Overexpression of p-p38 and uPA may play a critical role in breast cancer malignant progression. These results provide instructive clues to breast cancer invasion and metastasis research.

Key words: p-p38 uPA Breast cancer

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