白血病·淋巴瘤
白血病·淋巴瘤
백혈병·림파류
JOURNAL OF LEUKEMIA & LYMPHOMA
2013年
10期
578-581
,共4页
吴红艳%耿玲玲%刘志刚%董亚琳%何敏
吳紅豔%耿玲玲%劉誌剛%董亞琳%何敏
오홍염%경령령%류지강%동아림%하민
姜黄素%微乳%细胞增殖%细胞凋亡%基因,WT1
薑黃素%微乳%細胞增殖%細胞凋亡%基因,WT1
강황소%미유%세포증식%세포조망%기인,WT1
Curcumin%Microemulsion%Cell proliferation%Apoptosis%Gene,WT1
目的 研究姜黄素微乳对白血病K562细胞增殖与凋亡的影响.方法 制备姜黄素微乳,用四甲基偶氮唑蓝(MTT)方法观察其对K562细胞增殖作用的影响.用AnnexinV-PI双染、流式细胞术分析检测姜黄素微乳对K562细胞早期凋亡率的影响;用反转录PCR检测姜黄素微乳对K562细胞WT1基因表达的影响.均与姜黄素溶液处理的细胞进行比较.结果 制备的姜黄素微乳澄清透明,特性稳定,能剂量依赖性抑制K562细胞的增殖率,2.5、5、10 μg/ml姜黄素微乳作用24 h,细胞增殖抑制率为24%、46%、68%,而同等浓度姜黄素溶液处理后细胞增殖抑制率分别为6%、14%、25%.姜黄素微乳促凋亡作用也优于姜黄素溶液.姜黄素微乳抑制K562细胞WT1 mRNA表达的作用(0.190±0.036)也较姜黄素溶液(0.456±0.047)强.结论 以微乳为载体的姜黄素性状稳定.姜黄素微乳在抑制K562细胞增殖、促进凋亡及抑制WT1基因表达方面均显著强于普通姜黄素溶液.为临床应用姜黄素微乳治疗肿瘤提供了有力的理论依据.
目的 研究薑黃素微乳對白血病K562細胞增殖與凋亡的影響.方法 製備薑黃素微乳,用四甲基偶氮唑藍(MTT)方法觀察其對K562細胞增殖作用的影響.用AnnexinV-PI雙染、流式細胞術分析檢測薑黃素微乳對K562細胞早期凋亡率的影響;用反轉錄PCR檢測薑黃素微乳對K562細胞WT1基因錶達的影響.均與薑黃素溶液處理的細胞進行比較.結果 製備的薑黃素微乳澄清透明,特性穩定,能劑量依賴性抑製K562細胞的增殖率,2.5、5、10 μg/ml薑黃素微乳作用24 h,細胞增殖抑製率為24%、46%、68%,而同等濃度薑黃素溶液處理後細胞增殖抑製率分彆為6%、14%、25%.薑黃素微乳促凋亡作用也優于薑黃素溶液.薑黃素微乳抑製K562細胞WT1 mRNA錶達的作用(0.190±0.036)也較薑黃素溶液(0.456±0.047)彊.結論 以微乳為載體的薑黃素性狀穩定.薑黃素微乳在抑製K562細胞增殖、促進凋亡及抑製WT1基因錶達方麵均顯著彊于普通薑黃素溶液.為臨床應用薑黃素微乳治療腫瘤提供瞭有力的理論依據.
목적 연구강황소미유대백혈병K562세포증식여조망적영향.방법 제비강황소미유,용사갑기우담서람(MTT)방법관찰기대K562세포증식작용적영향.용AnnexinV-PI쌍염、류식세포술분석검측강황소미유대K562세포조기조망솔적영향;용반전록PCR검측강황소미유대K562세포WT1기인표체적영향.균여강황소용액처리적세포진행비교.결과 제비적강황소미유징청투명,특성은정,능제량의뢰성억제K562세포적증식솔,2.5、5、10 μg/ml강황소미유작용24 h,세포증식억제솔위24%、46%、68%,이동등농도강황소용액처리후세포증식억제솔분별위6%、14%、25%.강황소미유촉조망작용야우우강황소용액.강황소미유억제K562세포WT1 mRNA표체적작용(0.190±0.036)야교강황소용액(0.456±0.047)강.결론 이미유위재체적강황소성상은정.강황소미유재억제K562세포증식、촉진조망급억제WT1기인표체방면균현저강우보통강황소용액.위림상응용강황소미유치료종류제공료유력적이론의거.
Objective To determine the effects of curcumin microemulsion on proliferation and apoptosis of the human leukemia cell line K562 cells.Methods The curcumin microemulsion was prepared with the routine procedure.MTT assay was used to determine cell proliferation in cultured K562 cells,flow cytometry analysis was applied to examine cell apoptosis,and WT1 mRNA was determined with RT-PCR.The results about curcumin microemulsion were compared with these on curcumin.Results The prepared curcumin microemulsion was a stable clear solution with diameter of 10-100 nm.Curcumin microemulsion inhibited K562 cell proliferation by 24%,46%,68%with a 24 h incubation at dose of 2.5 μg/ml,5.0 μg/ml,and 10.0 μg/ml respectively,whereas curcumin reduced the proliferation by 6%,14%,25%at equal concentrations.WT1 mRNA level of curcumin microemulsion group(0.190±0.036)was reduced stronger than that of curcusin group(0.456±0.047).Conclusions Microemulsion is a great carrier for curcumin.Curcumin microemulsion is more effective in inhibiting proliferation,pro-apoptosis,and reducing WT1 gene expression than curcumin.A strong basis of medical value for the use of curcumin microemulsion to treat tumors is provided.