Effects of a new matrix metalloproteinase inhibitor, MMI-166, in nude mouse xenografts of human pancreatic cancer
10.3760/cma.j.issn.1007-8118.2012.11.014
- VernacularTitle:新型基质金属蛋白酶抑制剂MMI-166对裸鼠胰腺癌移植瘤作用的研究
- Author:
Huaiyong XU
;
Bengang GONG
;
Chongchong GAO
;
Mengyu LI
;
Junben WU
;
Tinghai XIANG
;
Piguang CHENG
- Publication Type:Journal Article
- Keywords:
Pancreatic neoplasms;
Protease inhibitors;
Matrix metalloproteinases;
Apoptosis
- From:
Chinese Journal of Hepatobiliary Surgery
2012;(11):859-862
- CountryChina
- Language:Chinese
-
Abstract:
Objective To investigate of the MMI-166 on the expression of MMP-2,MMP-9 and the cell apoptosis of nude mouse xenografts of SW1990 human pancreatic cancer cells.Methods Establishment of control and experimental groups,randomly,the human pancreatic cancer xenograft model of SW1990 was constructed.The control group was treated with normal saline,and experimental group was treated with MML-166 (200 mg · kg-1 · d-1).The tumor volume and tumor inhibition rate was measured by vernier caliper through length and short diameter.The expression of MMP-2 and MMP-9 protein was observed using immunohistochemistry in the tumor tissues.Apoptosis index was detected by deoxynucleotidyl transferase-mediated nick end labeling (TUNEL method).Results The tumor volume of MMI-166 group (1252.30± 464.84) mm3 was less than the control group (2241.82±208.06) mm3,significantly.The inhibition rate was 34.47％ between the experimental groups (treat with MMI-166) (1.42±0.15) g and control group (2.17±0.20) g.The expression of MMP-2 (2.80 ± 1.10) ％ and MMP-9 (2.60 ± 1.52) ％ protein was significantly downregulated in MMI-166 group,compared with the control group.Apoptotic index in the experimental group (75.60±9.71) ％ was higher than the control group (17.40 ± 10.14) ％,significantly.Conclusion The mechanism of MMI-166 inhibiting pancreatic tumor growth and inducing apoptosis may be related to the suppression of MMP-2 and MMP-9 protein expression.
