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作 者:曾曼丽[1] 孙文忠[2] 徐志文[1] 魏媛媛[1] 郑实兴[1]
机构地区:[1]广西医科大学第一附属医院耳鼻喉-头颈外科南宁市530021 [2]广西柳州市人民医院耳鼻喉-头颈外科
出 处:《中国肿瘤临床》2012年第10期634-638,共5页Chinese Journal of Clinical Oncology
基 金:广西科学基金项目(编号:桂科自0728241)资助~~
摘 要:目的:通过观察海带多糖(laminaria japonica polysaccharides,LJP)在体内外对人鼻咽癌(nasopharyngeal carcinoma,NPC)细胞的抑制作用,探讨其可能的抗癌机制。方法:应用MTT法检测LJP对人NPC细胞株(HONE1和CNE2)增殖的抑制作用;运用PI加Annexin V双染法检测LJP对HONE1细胞凋亡的影响;以人NPC细胞株HONE1建立裸鼠皮下移植瘤模型及行体内抑瘤实验,并在透射电镜(transmission electron microscopy,TEM)下观察移植瘤细胞超微结构。结果:MTT显示LJP对人NPC细胞(HONE1和CNE2)的增殖有抑制作用,且具有剂量相关性,320 mg/L的LJP作用72h的抑制率分别为58.27%(P<0.01)和55.00%(P<0.01);流式细胞仪检测结果显示,LJP具有诱导HONE1细胞凋亡的作用,凋亡率随着LJP浓度的增加而增高,320mg/L的凋亡率为(49.51±1.89)%(P<0.01)。体内实验中,LJP中、高剂量组抑瘤率分别为33.7%(P<0.05)和47.0%(P<0.01),具有明显抑制移植瘤的作用,而低剂量组的抑瘤率仅为16.4%(P>0.05)。TEM结果提示癌细胞呈现凋亡特征的改变。结论:LJP具有抑制NPC细胞生长的作用,机制可能是通过诱导癌细胞凋亡而实现的。Objective: This study aims to evaluate the antitumor activity of Laminaria japonica polysaccharides ( LJP ) on human nasopharyngeal carcinoma ( NPC ) cells in vitro and in vivo, and to explore the underlying mechanisms. Methods: Different human NPC cell lines were treated with LJP, and cell proliferation was examined by MTT assays. The cell apoptosis of LJP-treated HONE1 was examined by double staining assay. A tumor model established by the subcutaneous inoculation of NPC cell HONE1 into nude mice was used to evaluate the inhibitory action of LJP in vivo. Transmission electron microscopy ( TEM ) was used to observe changes in the ultrastructure of the NPC cells in xenografts. Results: The anti-proliferative activity of LJP was found in both human NPC cell lines ( HONE1 and CNE2 ) by MTT assay. Flow cytometry showed that LJP can induce the apoptosis of HONE1. With increased con- centration of LJP, the apoptosis rate increased. The apoptosis rate was 49.51% ± 1.89 % ( P 〈 0.01 ) when treated with 320 mg/L LJP. The inhibition ratio was between 50 % and 60 % at 72 h after treatment with 320 mg/L LJP. Compared with the control group, the growth of xenografts in nude mice was significantly suppressed following the administration of LJP in a dose-dependent manner. The inhibition ratios were 33.7 % ( P 〈 0.05 ) and 47.0 % ( P 〈 0.01 ) when treated with 25 mg/kg and 50 mg/kg LJP, respectively. Howev- er, the inhibition ratio of the 12.5 mg/kg group was only 16.4 % ( P 〉 0,05 ). The typical morphological changes in apoptosis were re- vealed by TEM. Conclusion: LJP can inhibit the growth of NPC probably by inducing the apoptosis of NPC cells in vitro and in vivo.
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