Wu Jian,Zhang Min,Dai Tianyang,Ren Delian.Biological effects of MACC1 siRNA interference on esophageal carcinoma TE-1 cells[J].J Amry Med Univ (J Third Mil Med Univ),2014,36(05):442-445.
Wu Jian,Zhang Min,Dai Tianyang,Ren Delian.Biological effects of MACC1 siRNA interference on esophageal carcinoma TE-1 cells[J].J Amry Med Univ (J Third Mil Med Univ),2014,36(05):442-445.DOI:
Biological effects of MACC1 siRNA interference on esophageal carcinoma TE-1 cells
Objective To determine the effects of siRNA interfering metastasis-associated in colon cancer 1 (MACC1) on the extracorporeal proliferation
migration and invasion of the esophageal squamous cell carcinoma (ESCC) cell line TE-1. Methods The special MACC1-siRNA sequence was chemically synthesize
and then transfected into the T
E-1 cells with lipofectamine
TM
2000. RT-quantity PCR and Western blotting were used to detect the mRNA and protein level of MACC1 in untreated TE-1 cells
lipo2000-treated cells (mock)
siRNA-nc transfected cells
and siRNA-MACC1 transfected cells. MTT assay was used to detect the proliferation of TE-1 cells. Scratching test and Transwell chamber assay were evaluated the migration of the cells. Results Compared with the untreated cell
mock
and siRNA-nc cells
the expression of MACC1 was obviously decreased by 71% at mRNA and 87% at protein levels. In 7 dafter transfection
MTT assay indicated that the proliferation of the transfected TE-1 cells was significantly inhibited compared with the other 3 types of cells (
P
0.05)
especially from the fourth day. Scratching test showed that there were obviously less migrated cells from the siRNA-MACC1 group than those from the control (10.6±2.2 vs 68.2±2.5
P
0.05). Transwell assay also showed the invasion ability of TE-1 cells transfected with siRNA-Macc1 was lesser than the control cells (4.2±1.92 vs 58.4±7.44
P
0.05). But no significant difference was seen among the untreated cell
mock
and siRNA-nc cells. Conclusion siRNA interference of MACC1 obviously down-regulates the molecule at mRNA and protein levels in TE-1 cells
and results in significant inhibition in the proliferation
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