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二烯丙基二硫对人胃癌MGC803细胞生长的影响 被引量:29

Inhibitory effect of diallyl disulfide on human gastric cancer cell line MGC803 in vitro
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摘要 目的:研究二烯丙基二硫(DADS)对人胃癌MGC803细胞生长的抑制作用。方法:采用MTT法、生长曲线分析、细胞活力检测、双层软琼脂集落形成率、及倒置显微镜等方法,观察DADS对体外培养的人胃癌MGC803细胞的影响。结果:DADS对MGC803细胞具有明显的生长抑制效应,且呈剂量-效应依赖关系(P<0.05)。培养96 h,35mg/LDADS的抑制作用呈时间-效应依赖关系(P<0.05)。细胞群体倍增时间由33.8 h处长至DADS处理后的84.0 h(P<0.05);细胞存活率分别为阴性对照组97.4%和DADS处理组80.4%(P>0.05);软琼脂集落形成率由 1.23%下降到0.33%(P<0.05)。阴性对照组细胞多角形、圆形,体积大,多形性明显,核大小不一,见双核及核仁,细胞生长紧密呈堆叠生长,DADS处理后细胞异型性降低,为形态一致的梭形,体积小,境界清楚而分散,胞质丰富,核明显变小。结论:DADS对体外培养的MGC803细胞具有明显的增生抑制作用,且呈现剂量-效应依赖关系。 AIM: To investigate the effect of diallyl disulfide(DADS) on human gastric cancer MGC803 cell line in vitro. METHODS: The effect of DADS was confirmed by MTT assay, cell growth curve analysis, cell viability detection, clony formation in soft agar and inversion microscopy. RESULTS: In vitro growth of MGC803 cells was significantly inhibited by DADS in a dose-dependent manner (P<0.05) when MGC803 cells were cultured for 96 hours, and at a higher concentration of 35 mg/L. The inhibiting effect of DADS displayed a time-dependent manner (P<0.05). Cell viability decreased from 97.4 % in negative control group to 80.4 % in treatment group. There was no significance existed between the two groups (P>0.05), and average doubling time was delayed from 33.75 h in negative control group to 84.0 h in treatment group (P<0.05).Clony for- mation ratio was also decreased from 1.23 % in negative control group to 0.33% in treatment group (P<0.05). After treated by DADS, MGC803 cells showed plemorphic and atypia declining, small size, uniform spindle shape, abun- dant cytoplasm and smaller nuclei.All these appeared in 20 mL/L DMSO treated MGC803 cells as well as in DADS- expose cells. CONCLUSION: The effect of growth inhibition of DADS on human gastric cancer MGC803 cells in vitro is Signifecant and exhibits a dose-dependent manner.
出处 《世界华人消化杂志》 CAS 2003年第9期1290-1293,共4页 World Chinese Journal of Digestology
基金 湖南省科委基金 No.97610319 No.00SSY3019 湖南省自然科学基金 No.01JJY2146 No.02JJY2026
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