Effect on cell proliferation and proteolytic enzyme of human gastric carcinoma by MUC2 antisense oligodeoxynucleotide in vitro
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Effect on cell proliferation and proteolytic enzyme of human gastric carcinoma by MUC2 antisense oligodeoxynucleotide in vitro
Journal of Army Medical UniversityVol. 29, Issue 6, Pages: 498-502(2007)
作者机构:
1. 重庆医科大学:附属第二医院普通外科,基础医学院病理学教研室
2. 山东省临沂市中心医院
作者简介:
基金信息:
DOI:
CLC:R73-354;R735.2;R730.23
Published:2007,
Published Online:30 March 2007,
稿件说明:
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LUO WEN-JUN, YI YONG-FEN, ZHANG XIAO-YAN, et al. Effect on cell proliferation and proteolytic enzyme of human gastric carcinoma by MUC2 antisense oligodeoxynucleotide in vitro. [J]. Journal of army medical university, 2007, 29(6): 498-502.
DOI:
LUO WEN-JUN, YI YONG-FEN, ZHANG XIAO-YAN, et al. Effect on cell proliferation and proteolytic enzyme of human gastric carcinoma by MUC2 antisense oligodeoxynucleotide in vitro. [J]. Journal of army medical university, 2007, 29(6): 498-502.DOI:
Effect on cell proliferation and proteolytic enzyme of human gastric carcinoma by MUC2 antisense oligodeoxynucleotide in vitro
of mucin gene MUC2 antisense oligodeoxynucleotide (ASODN) on its gene expression and proteolytic enzyme on gastric cancer cell line. Methods Phosphorothioated MUC2 ASODN were synthesized and transfected to SGC7901 cells mediated by lipofectin. MUC2 mRNA and MUC2 protein expressed on SGC7901 cells was detected by RT-PCR and immun
ohistochemical method. The inhibitory effects of ASODN on proteolytic enzyme
such as cathepsin D
MMP-2 and MMP-9 protein were detected by immunohistochemical staining. The cell cycle and apoptosis were determined by flow cytometry (FCM). Results The inhibition effects peaked at 48th hour after transfection
and the inhibition rate reached 55% when the concentration of ASODN was 0.5 μmol/L. The number of the cells treated with MUC2 ASODN was decreased as compared to the control cells. MUC2 ASODN transfection could inhibit the transition period of S phase to G
2
/M phase
and G
2
/M did not change much. The apoptosis rate was about 4.38%. As compared with blank control group
MUC2 ASODN could significantly inhibit MUC2 mRNA expression of SGC7901 cells. ASODN could downregulate the expression levels of MUC2 protein
MMP-2 and cathepsin D protein. Conclusion MUC2 ASODN transfection could specifically inhibit SGC7901 cells by downregulating the expression levels of proteolytic enzyme.