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1.
Zhonghua Zhong Liu Za Zhi ; 35(7): 497-500, 2013 Jul.
Artigo em Chinês | MEDLINE | ID: mdl-24257299

RESUMO

OBJECTIVE: To explore the molecular mechanism of miR-124 suppressing the proliferation and invasion of gastric cancer cells. METHODS: SPHK1 3'UTR-luciferase vector was constructed and luciferase reporter gene assay was employed to examine the effect of miR-124 on luciferase activity. Human gastric cancer MGC-803 cells were transfected with miR-124 mimics, and then Western blot was performed to detect the expression of SPHK1 protein. RESULTS: Luciferase reporter vector system confirmed that SPHK1 was a target gene of miR-124. Western blot showed that the expression of SPHK1 protein was inhibited by miR-124. After transfection of miR-124 mimics or SPHK1 siRNA for 12 h, 24 h and 48 h, respectively, MTT assay showed that the A values of the three groups were significantly different (P < 0.05), and it was in a time-dependent manner. After transfection of miR-124 mimics or SPHK1 siRNA for 24 h, transwell invasion assay showed that the number of transmembrane cells was 54.6 ± 8.3 in the SPHK1 siRNA group and 47.8 ± 6.6 in the miR-124 mimics group, both were significantly lower than 100.6 ± 11.3 of the control group (P < 0.05), indicating that SPHK1 siRNA can slow down the invasion of MGC-803 cells. CONCLUSION: miR-124 can suppress the cell proliferation and invasion by targeting SPHK1 in gastric carcinoma.


Assuntos
Proliferação de Células , MicroRNAs/genética , Fosfotransferases (Aceptor do Grupo Álcool)/metabolismo , Neoplasias Gástricas/patologia , Linhagem Celular Tumoral , Vetores Genéticos , Humanos , Luciferases/genética , Luciferases/metabolismo , Invasividade Neoplásica , Fosfotransferases (Aceptor do Grupo Álcool)/genética , RNA Interferente Pequeno/genética , Proteínas Recombinantes/genética , Proteínas Recombinantes/metabolismo , Neoplasias Gástricas/metabolismo , Transfecção
2.
Cell Mol Biol Lett ; 11(3): 408-23, 2006.
Artigo em Inglês | MEDLINE | ID: mdl-16874458

RESUMO

Diallyl disulfide (DADS) is a major constituent of garlic. Previously, we found that DADS both inhibited proliferation in human gastric cancer cells in vitro and in vivo, and induced G2/M arrest. In this study, we investigated whether this differentiation effect was induced by DADS in human gastric cancer MGC803 cells, and whether it was related to an alteration in ERK activity. The results showed that the growth of MGC803 cells was inhibited by DADS. Cells treated with DADS displayed a lower nucleocytoplasmic ratio and tended to form gland and intercellular conjunction structures. The ConA-mediated cell agglutination ratio and cells' ALP specific activity decreased. In MGC803 cells, dye transfer was limited to a few cells neighbouring the dye-injected cell and to a depth of 1-2 layers beneath the scrape site. However, after treatment with DADS, the LY (Lucifer Yellow) was transferred to several cells immediately neighbouring the microinjected cell and to a depth of 2-4 cell layers from the scrape site. This indicated that DADS induced differentiation in MGC803 cells. Western blot analysis revealed that although DADS did not influence the quantity of ERK1/2 protein expressed, it did decrease its phosphorylation in a concentration-dependent manner, compared with the controls. At 30 mg x L(-1), DADS inhibited the activation of ERK1/2 in 15-30 min. These results suggested that the DADS-induced differentiation of MGC803 cells involved an alteration of the ERK1/2 signaling pathway.


Assuntos
Compostos Alílicos/farmacologia , Diferenciação Celular/efeitos dos fármacos , Dissulfetos/farmacologia , Proteína Quinase 1 Ativada por Mitógeno/metabolismo , Proteína Quinase 3 Ativada por Mitógeno/metabolismo , Neoplasias Gástricas/enzimologia , Neoplasias Gástricas/patologia , Aglutinação/efeitos dos fármacos , Fosfatase Alcalina/metabolismo , Butadienos/farmacologia , Linhagem Celular Tumoral , Sobrevivência Celular/efeitos dos fármacos , Concanavalina A/farmacologia , Humanos , Nitrilas/farmacologia , Fosfoproteínas/metabolismo , Fosforilação/efeitos dos fármacos , Neoplasias Gástricas/ultraestrutura
3.
World J Gastroenterol ; 4(1): 29, 1998 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-11819224

RESUMO

INTRODUCTION:To study effect of garlic and garlic-green tea mixture on serum contents of Tch,LDL and HDL in MNNG induced gastric carcinoma (GC) and precancerous lesion (PL) in Wistar rats.METHODS:Serum contents of Tch,LDL and HDL in normal control group (n=10,NG),MNNG group (n=30,MG),prevention group (n=30,PG),treatment group I (n=20,TG I) and treatment group II(n=20,TG II) were detected by PGE 6000/COD.RESULTS:Serum Tch and LDL of rats of MG (6.86±1.39 3.72±1.10) and its GC(6.95±1.37 3.77±1.08) and PL(6.42±1.04 3.56±0.74) were lower than that of NG (8.74±1.89 5.89±1.61) PG(7.73±3.18 4.96±2.89) and its GC(8.36±3.41 5.93±3.31) and PL(7.45±3.16 4.55±2.71),TGI(8.86±1.75 5.38±1.76) and its GC (9.10±2.27 5.55±2.51) and PL (8.61±1.17 5.22±0.55) and TG II (8.16±0.76 5.32±0.72) and its GC(8.52±0.67 5.96±0.48) and PL (8.02±0.79 5.09±0.65),respectively (P <0.01-0.05).Serum HDL of MG rats (2.76±0.48) and its GC(2.79±0.48) were remarkably higher than that of MG (2.20±0.85) and GC of PG (2.24±0.38) (P <0.05).CONCLUSION:Experimental gastric carcinoma and precancerous lesion were associated with hypocholesterolaemia,LDL and HDL.Garlic and garlic-green tea mixture can inhibit and reverse MNNG-induced gastric carcinoma and precancerous lesion in Wistar rats.

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