›› 2011, Vol. 23 ›› Issue (3): 190-193.doi: 10.3969/j.issn.1004-616x.2011.03.007

• 论著 • Previous Articles     Next Articles

The expression and significance of MMP-1,,MMP-2, MMP-7, TIMP-1 and MTA1 in esophageal cancer of Kazaks

LI Xiu-mei1,CHEN Yan1,WANG Hong-jiang2,PANG Zuo-liang2,LI Hui1,JIANG Xiao-fang1,Gulinuer·Muhayi1,CHEN Hong-ming1,LI Hui-wu1,*   

  1. 1. School of Basic Medicine; 2. The Affiliated Tumour Hospital, Xinjiang Medical University, Urumqi 830011, Xinjiang, China
  • Received:2011-03-06 Revised:2011-03-24 Online:2011-05-30 Published:2011-05-30
  • Contact: LI Hui-wu

Abstract: To study expressions of matrix metalloproteinase1,2,7 ( MMP-1,MMP-2,MMP-7),tissue inhibitor of matrix metallo proteinase 1(TIMP-1) and metastasis associated gene 1 (MTA1)in esophageal cancer tissue and normal tissue among Kazaks and to investigate the relationship between their expressions and clinical pathological features. METHODS:Using RT-PCR to detect the expressions of MMP-1,MMP-2,MMP-7,TIMP-1 and MTA1 in 75 esophageal cancer specimens. RESULTS:The mRNA expressions of MMP-1,MMP-2,MMP-7 ,TIMP-1 and MTA1 in cancer tissue were higher than those of normal tissues(P<0.05).While the expression levels of MMP-2,MMP-7 and MTA1 mRNA were significantly related to the lymph node metastasis. The expression levels of MMP-1,MMP-7 mRNA were significantly related to the TNM stages(P<0.05). The expression of TIMP-1 in the Kazak's esophageal cancer was positively related to the expressions of MMP-1,MMP-7,MTA1 ( r = 0.446、0.458、0.333,respectively, P<0.01 ). CONCLUSION:The overexpressions of MMP-1,MMP-2,MMP-7,TIMP-1 and MTA1 gene could have important roles in carcinogenesis of esophageal cancer in the Kazaks. Their synergistic effect could promote carcinogenesis and development of esophageal cancer. The MMP-2,MMP-7 and MTA1 genes may be the main players of progression and metastasis in esophageal cancer among Kazaks.

Key words: esophageal cancer, matrix metalloproteinase, tissue inhibitor of matrix metalloproteinase 1, metastasis associated gene 1