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作 者:李学农[1] 丁彦青[1] 周军[1] 朱梅刚[1]
机构地区:[1]第一军医大学病理学教研室,广东广州510515
出 处:《癌症》2000年第11期969-973,共5页Chinese Journal of Cancer
基 金:国家自然科学基金! 39770912);军队医药卫生基金!(96Q47)资助
摘 要:目的: 研究蓼科植物阴阳莲提取物 3, 4, 5-三羟基芪- 3-β-单- D-葡萄糖苷( 3, 4, 5,- trihydroxystibene- 3-β- mono- D- glucoside, THMG)对大肠癌细胞的体外生长特性、粘附性及浸润力的影响;从细胞层次探讨 THMG抗转移作用的基本环节。方法:检测 4种大肠癌细胞( HR8348, Hce8693, HT29, LoVo)在 THMG 0.4 mmol/L, 0.8 mmol/L, 1.6 mmol/L, 3.2 mmol/L等浓度作用下的存活率、生长曲线、粘附率及浸润力。结果:在实验浓度下, THMG对 4种大肠癌细胞的存活率、生长曲线无显著影响( P >0.05),在 3.2 mmol/L浓度时对高转移性的 LoVo细胞的粘附抑制率为 68.09% ,浸润抑制率为 89.95% ,对低转移性的 HT29细胞粘附抑制率为 78.75%、浸润抑制率为 93.31%,且随着浓度加大,粘附和浸润抑制率提高。结论: THMG可能通过抑制癌细胞粘附性和浸润力,发挥抗转移效应。Objective: The current study was designed to investigate anti- adhesion and anti- invasion effects of 3, 4′, 5- trihydroxystibene- 3-β- mono- D- glucoside (THMG) on colorectal carcinoma cell lines in vitro. Methods: Four cell lines (HR8348, Hce8693, HT29 and LoVo) from human colorectal carcinoma were treated with 0.4 mmol/L, 0.8 mmol/L, 1.6 mmol/L and 3.2 mmol/L of THMG. Cell viability was assessed by trypanblue exclusion test. Adhesion test and quantitative invasion assay were performed by using modified human amniotic basement membrane (HABM)model and Boyden chamber model,respectively. Results: At the experimental concentration, THMG had no significant effects in terms of cell viability and cell growth curve on the colorectal carcinoma cell lines while at the concentration of 3.2 mmol/L THMG could markedly inhibit adhesion to HABM, with inhibit rate of 68.09% for highly metastatic cell line(LoVo) and of 78.75% for low metastatic cell line (HT29),respectively. Invasion inhibit rate determined by Matrigel invasion assay was 89.95% for highly invasive cell line(LoVo), and 93.31% for low invasive cell line(HT29), respectively. The adhesion inhibit rate and invasion inhibit rate were enhanced according to the concentration of THMG. Conclusion: THMG, an effective component from Chinese herb (polygonum cuspidatum sieb. et zucc), may have anti- metastasis effect through inhibit adhesiveness and invasiveness of colorectal carcinoma cells.
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