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1.
Journal of Sun Yat-sen University(Medical Sciences) ; (6): 264-269, 2019.
Artigo em Chinês | WPRIM | ID: wpr-817749

RESUMO

@#【Objective】Serum gamma-glutamyltransferase(GGT)has recently been implicated in the pathogenesis of atherosclerosis and coronary heart disease(CHD). We aimed to evaluate the association between the serum GGT level and the 10-year risk score for CHD(Framingham Risk Score,FRS)in a Chinese population.【Methods】We conducted a population-based cross-sectional study in 9,544 Guangzhou residents aged 40 years and older. Participants were divided into four quartiles according to their GGT levels:Quartile 1 <15 U/L(n=2 407),Quartile 2 15~19.9 U/L(n=2 302), Quartile 3 20~28.9 U/L(n=2 442),and Quartile 4 ≥29 U/L(n=2 393). The multivariate logistic regression analysis was used to assess the incidence of intermediate and high risk of developing CHD at 10 years(FRS≥10%)in relation to each quartile increase of serum GGT level.【Results】The incidence of FRS≥10% increased with elevating serum GGT levels(P for trend<0.001). Compared with the lowest quartile of serum GGT level ,the adjusted odds ratio in the highest quartile was 1.72(95% confidence interval 1.28 to 2.29).【Conclusion】Serum GGT level is associated with the FRS for CHD ,and might be used as an adjuvant marker for identifying patients at increased risk of cardiovascular events and early intervention.

2.
Journal of Experimental Hematology ; (6): 43-47, 2012.
Artigo em Chinês | WPRIM | ID: wpr-331025

RESUMO

The study was aimed to investigate the synergistically effect of interferon-α (IFN-α) and homoharringtonine (HHT) on the proliferation, apoptosis, cell cycle of K562 cells and the expression of β-catenin. The proliferation, apoptosis, cell cycle and β-catenin mRNA expression of K562 cells treated with IFN-α and/or HHT were assayed with MTT, flow cytometry or RT-PCR respectively. The results showed that HHT alone, but not IFN-α alone, displayed a proliferation inhibition, apoptosis induction, G(0)/G(1) phase block and down-regulation of β-catenin expression in K562 cells with concentration- and time-dependent manners. The expression level of β-catenin mRNA after being treated with HHT was 0.5576 ± 0.0373, which were lower than that in control group (0.9369 ± 0.0142). The down-regulation of β-catenin expression in group of IFN-α combined with HHT was higher significantly than that in HHT group (0.3737 ± 0.0529 vs 0.5576 ± 0.0373, P < 0.05). Otherwise, HHT combined with IFN-α did not demonstrate obvious toxicologic effect on bone marrow mononuclear cells. It is concluded that IFN-α combined with HHT can enhance the cytotoxic effect of HHT on K562 cells, which may be associated with down-regulation of β-catenin expression.


Assuntos
Humanos , Proliferação de Células , Harringtoninas , Farmacologia , Interferon-alfa , Farmacologia , Células K562 , beta Catenina , Genética , Metabolismo
3.
Chinese Medical Journal ; (24): 517-522, 2012.
Artigo em Inglês | WPRIM | ID: wpr-262580

RESUMO

<p><b>BACKGROUND</b>Interferon-induced transmembrane protein 1 (IFITM1) has been identified as a molecular marker of the colorectal tumors; however its influences on the biological behaviors of the colorectal cancer cells are currently unknown. We aimed to study the influences of IFITM1 on the proliferation, invasion, and metastasis of the colorectal cancer SW480 cell lines.</p><p><b>METHODS</b>We constructed IFITM1/pEGFP-C3 recombinant plasmids and transfected them into the colorectal cancer SW480 cell lines. IFITM1/pEGFP-C3 recombinant plasmids were identified by means of immunofluorescence, laser confocal scanning microscopy, and reverse transcription polymerase chain reaction. IFITM1/SW480 cells with stable over-expression of IFITM1 were confirmed by G418 screening. The influences of IFITM1 on the proliferation of the SW480 cell lines were investigated by MTT assay and tumor transplantation experiments in nude mice. Cell invasion experiments were performed to determine the invasion capacity of the IFITM1/SW480 cells. Matrix metalloproteinase 2 (MMP-2) and MMP-9 activities were detected by the gelatin zymographic analysis, and MMP-9 expression by the Western blotting analysis.</p><p><b>RESULTS</b>IFITM1/pEGFP-C3 recombinant plasmids were successfully constructed in this study, and the IFITM1/SW480 cells with stable IFITM1 gene over-expression were confirmed by G418 screening. MTT results showed that the proliferation of the IFITM1/SW480 cells was significantly enhanced (P < 0.01). Tumors were harvested from four weeks old mice. Tumor volumes were (1347.00 ± 60.94) mm(3), (1032.40 ± 111.38) mm(3) and (1018.78 ± 28.83) mm(3); and tumor weights were (1522.34 ± 62.76) mg, (1137.78 ± 97.22) mg and (1155.76 ± 133.31) mg for mice inoculated with the IFITM1/SW480 cells, pEGFP-C3/SW480 cells and SW480 cells, respectively. Tumor volumes and weights from mice inoculated with the IFITM1/SW480 cells were significantly increased (P < 0.01). In addition, the numbers of the SW480 cells and IFITM1/SW480 cells that migrated through Matrigel were 448.64 ± 38.09 and 540.45 ± 44.61, respectively; so the invasive ability of the SW480 cells transfected with IFITM1 gene was significantly greater than that of the SW480 cells (P < 0.01). Gelatin zymographic analysis showed that MMP-9 and MMP-2 protein activities in the IFITM1/SW480 cells were significantly enhanced, and Western blotting analysis showed that MMP-9 expression in the IFITM1/SW480 cells was also increased.</p><p><b>CONCLUSION</b>IFITM1 can enhance the proliferation, invasion, and metastasis of the colorectal cancer SW480 cell lines.</p>


Assuntos
Humanos , Linhagem Celular Tumoral , Proliferação de Células , Neoplasias Colorretais , Metabolismo , Regulação Neoplásica da Expressão Gênica , Genética , Fisiologia , Metaloproteinase 2 da Matriz , Genética , Metabolismo , Metaloproteinase 9 da Matriz , Genética , Metabolismo , Plasmídeos , Proteínas de Transporte Vesicular , Genética , Metabolismo
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