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作 者:黄来珍[1] 王长秀[1] 马润娣[1] 于立坚[1] 苏伟明[1] 廖铭能[1] 于廷曦[1]
机构地区:[1]广东海洋大学海洋药物研究与开发重点实验室,湛江524025
出 处:《中国细胞生物学学报》2010年第2期223-228,共6页Chinese Journal of Cell Biology
基 金:国家自然科学基金项目(No.30271493);广东省自然科学基金重点项目(No.021386);广东省海洋与渔业局科技兴海重大项目(No.A200099B01)资助~~
摘 要:以小鼠Lewis肺癌(Lewis lung carcinoma,LLC)自发转移和小鼠黑色素瘤(B16)细胞实验转移为模型,检测福安泰-03(Fuantai-03,FAT-03)对小鼠Lewis肺癌生长和转移的影响,Western印迹和免疫组化法分析FAT-03对小鼠Lewis肺癌转移相关基因CD44和nm23-H1表达水平的影响。结果显示,FAT-03明显抑制LLC的生长和肝转移,显著抑制B16细胞的肺转移,并与环磷酰胺(CY)有协同作用。每天腹腔注射FAT-03 10.0、20.0 mg/kg,共用药14天,对LLC生长的抑制率分别为53.8%、61.3%(CY的抑制率为58.8%);对LLC肝转移的抑制率分别为37.4%、76.5%(CY的抑制率为64.5%)。对B16细胞肺转移的抑制率分别为51.4%和63.7%(CY的抑制率为44.0%,10.0mg/kg FAT-03+CY的抑制率为88.1%)。显著下调促癌转移基因CD44,上调抑癌转移基因nm23-H1的表达。结果提示FAT-03值得作为一种具有抗癌转移作用的先导物质继续研究,它的抗癌转移效果可能部分与其下调促癌转移基因CD44和上调抑癌转移基因nm23-H1的表达有关。Western blot analysis and immunohistochemistry protocol were performed to assay the expressions of CD44 and nm23-H1; mouse Lewis lung carcinoma (LLC), a spontaneous tumor metastasis model, and mouse B 16 melanoma (B 16), a experimental tumor metastasis model, were utilized to study the effects of intraperitoneal (ip) injection of Fuantai-03 (FAT-03) on cancer metastasis. The results showed that FAT-03 resulted in downregulation of expression of CD44, and up-regulation of expression of nm23-H1 in vitro and in vivo, and that the growth inhibition rates of primary tumors of LLC in the FAT-03 [10.0, 20.0 mg/(kg·d), ip, for 14 days]-administered mice were 53.8% and 61.3% [vs 58.8% of cyclophosphamide (CY) ], and the liver metastasis inhibition rates (MIR) of LLC were 37.4% and 76.5% (vs. 64.5% of CY), and the lung MIR of B16 were 51.4% and 63.7% (vs 44.0% of CY, and 88.1% of 10.0 mg/kg FAT-03+CY), respectively. These observations qualify FAT-03 as an interesting lead component to prevent cancer metastasis; FAT-03-induced change of expressions of metastasis-related genes may be partially responsble for its inhibitory effect on metastasis.
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