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葡萄糖与甘氨酸在亚硝酸钠存在下发生美拉德反应产物中的GGN-MRP提取物在C3H10T1/2细胞中的促肿瘤作用

Tumor-promoting effect of GGN-MRP extract from the Maillard reaction products of glucose and glycine in the presence of sodium nitrite in C3H10T1/2 cells.

作者信息

Chen C C, Tseng T H, Hsu J D, Wang C J

机构信息

Institute of Biochemistry, College of Medicine, Chung Shan Medical University, Taichung, Taiwan.

出版信息

J Agric Food Chem. 2001 Dec;49(12):6063-7. doi: 10.1021/jf0106897.

Abstract

GGN-MRP is an extract from the Maillard reaction products of nitrite with glucose and glycine in the Maillard browning system. No genotoxicity of GGN-MRP in culture hepatocyte was found. A two-stage transformation protocol was used to transform chemically mouse embryo fibroblast C3H10T1/2 cells. To initiate transformation, the cells were treated with benzo[a]pyrene [B(a)P; 0.1 microg/mL], and GGN-MRP (0.01, 0.1, and 1.0 mg/mL) was employed to subsequently complete the transformation process. Malignant transformed foci were formed in B(a)P-initiated and GGN-MRP-promoted C3H10T1/2 cells after 8 weeks. Cells treated with GGN-MRP alone failed to induce transformation. However, cells initiated with B(a)P and promoted by GGN-MRP demonstrated oncogenic properties. Transformed colonies derived from GGN-MRP-treated cells exhibited enhanced growth rate, anchorage independence, and tumorgenicity in animals relative to parent cells. These results indicated that GGN-MRP contains a tumor promoter and may induce tumor promotion by two-stage oncogenesis.

摘要

GGN-MRP是美拉德褐变体系中亚硝酸盐与葡萄糖和甘氨酸发生美拉德反应的产物提取物。未发现GGN-MRP对培养的肝细胞具有遗传毒性。采用两阶段转化方案对化学转化的小鼠胚胎成纤维细胞C3H10T1/2细胞进行转化。为启动转化,细胞用苯并[a]芘[B(a)P;0.1微克/毫升]处理,随后用GGN-MRP(0.01、0.1和1.0毫克/毫升)完成转化过程。8周后,在B(a)P启动和GGN-MRP促进的C3H10T1/2细胞中形成了恶性转化灶。单独用GGN-MRP处理的细胞未能诱导转化。然而,用B(a)P启动并由GGN-MRP促进的细胞表现出致癌特性。与亲代细胞相比,源自GGN-MRP处理细胞的转化菌落显示出在动物体内增强的生长速率、锚定非依赖性和致瘤性。这些结果表明,GGN-MRP含有肿瘤促进剂,可能通过两阶段肿瘤发生诱导肿瘤促进。

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