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作 者:马佰菁[1] 黄菱[1] 韩梅[1] 王玉巧[2] 赵建宁[1] 孙伯坚[1] 林佳静[1] 宋婷阁[1]
机构地区:[1]宁夏医科大学病原生物学与免疫学系,银川750004 [2]宁夏人民医院ICU
出 处:《中华肿瘤杂志》2011年第5期331-333,共3页Chinese Journal of Oncology
基 金:基金项目:宁夏自然科学基金(NZ1095);宁夏高等学校科学研究项目(2009-47)
摘 要:目的 研究赖氨酰氧化酶(LOX)对胃癌细胞HGC-27体外迁移和黏附能力的影响.方法 体外培养胃癌细胞HGC-27,以不同浓度的B-氨基丙腈(BAPN)抑制LOX的活性.采用体外划痕实验检测对细胞迁移能力的影响,采用同质黏附和异质黏附实验分析对细胞黏附能力的影响.结果 当BAPN浓度为0.2 mmol/L时,胃癌细胞的体外迁移能力在8、24、32、48 h各时间点均较未加BAPN下降(P〈0.05);且HGC-2q细胞在同质黏附介质上生长60 ndn后,同质黏附细胞数为(7.78±0.11)×103个/ml,与对照组[(6.97±O.07)×103个/ml]比较,差异有统计学意义(P〈0.05);异质黏附细胞数为(8.35±0.10)×103个/ml,与对照组[(8.98±0.15)×103个/ml]比较,差异有统计学意义(P〈0.05).当BAPN浓度为0.3 mmol/L时,胃癌细胞的体外迁移能力在各时间点均较未加BAPN下降,同质黏附细胞数增加至(8.02±0.11)×103个/ml,异质黏附细胞数减少至(7.93±0.07)×103个/ml,与对照组或0.2 mmol/L BAPN组比较,差异均有统计学意义(P〈0.05).结论 LOX可能通过促进肿瘤细胞的迁移和异质黏附能力,降低其同质黏附能力,促进肿瘤的转移.Objective To study the effects of lysyl oxidase ( LOX) on the migration and adhesion of the human gastric cancer cell line HGC-27 cells in vitro. Methods The human gastric cancer cell line HGC-27 cells were cultured in vitro, and treated with different concentration of β-aminopropionitrile (BAPN). The ability of migration was assessed by wound-healing assay. The ability of adhesion was detected by homogenous and heterogeneous adhesion experiments. Results Compared that with 0 mmol/L BAPN, the ability of migration of the cells after treatment with 0.2 mmol/L BAPN was descended at 8, 24, 32 and 48 h; the number of cells with homogeneous adhesion was increased from (6.97 ± 0.07) x l03/ml to (7.78±0.11) ×103/ml; and the number of cells with heterogeneous adhesion was decreased from (8.98± 0. 15) x 103/ml to (8. 35 ±0. 10) ×103/ml, both 〈0. 05. Compared with that of cells treated with 0 mmol/L and 0.2 mmol/L BAPN, the migration ability of cells after treatment with 0.3 mmol/L BAPN was descended at 8, 24, 32 and 48 h; the number of cells with homogeneous adhesion was raised to (8. 02 ± 0. 11) ×103/ml and the number of cells with heterogeneous adhesion was down to (7.93 ±0.07) ×103/ml (P 〈 0. 05). Conclusion LOX may promote the metastasis of cancer cells by enhancing invasion, increasing heterogeneous adhesion and decreasing homogeneous adhesion.
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