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机构地区:[1]中南大学湘雅三医院肿瘤科,长沙410013 [2]中南大学湘雅二医院妇科,长沙410011 [3]中南大学肿瘤研究所,长沙410078
出 处:《中南大学学报(医学版)》2007年第5期890-894,共5页Journal of Central South University :Medical Science
摘 要:目的:探讨槲皮素对小鼠宫颈癌U14的抗癌作用及其可能机制。方法:建立615近交系小鼠U14移植瘤动物模型,并随机分成4组:对照组、低剂量干预组[1.5g/(kg·d)]、中剂量干预组[3.0g/(kg·d)]及高剂量干预组[6.0g/(kg·d)],腹腔注射给药,连续用药20d,于接种后26d处死各组小鼠,检测各组小鼠的瘤体平均质量并计算抑瘤率,采用免疫组织化学半定量检测肿瘤组织微血管密度(MVD)及核因子-κB(NF-κB)表达水平,用原位TdT检测法(TUNEL)检测肿瘤细胞凋亡指数(AI)。结果:高剂量干预组肿瘤的生长明显受到抑制,肿瘤体积和瘤质量均明显低于对照组(P<0.01),其抑瘤率显著高于低、中剂量干预组(P<0.01);高剂量干预组MVD及NF-κB表达水平明显降低,AI则明显升高,与对照组比较,差异均有统计学意义(P<0.01),但低、中剂量槲皮素对MVD,NF-κB表达及AI无明显影响(P>0.05)。结论:槲皮素对小鼠宫颈癌的生长具有显著的抑制作用,其抗癌机制可能与抑制微血管生成和促进细胞凋亡有关。Objective To investigate the antitumor effect and mechanism of quercetin on mufine cervical carcinomal U14. Methods The 615-strain mice with U14 cervical cancer cells were randomly divided into 4 groups: a control, a low-dose intervention group [ 1.5 g/(kg·d) ] , a mid- dle-dose intervention group [ 3.0 g/( kg·d) ] , and a high-dose intervention group [6.0 g/( kg·d ) ] . Different treatments were inoculated intraperitoneally after 6 days of transplantation and all mice were sacrificed after 26 days. The weight of tumors and inhibitory rates were measured. The expression levels of microvessel density ( MVD ) and nuclear factor- KappaB ( NF-κB ) were detected by immunhistochemistry. The apoptosis index (AI) was measured by terminal deoxynucleotydyl transferase assay in situ (TUNEL). Results Compared with the control group, the tumor growth in the high-dose intervention group was suppressed significantly, and the weight and volume of the tumor were markedly decreased (P 〈0.01 ). The inhibitory rate in the high-dose intervention group was higher than that in the low- and middle-dose groups ( P 〈 0. 05 ) . The expression levels of NF-κB and MVD were significantly decreased, and AI was enhanced in the high-dose intervention group (P 〈0.01). However, the low- and middle-dose quercetin had no obvious influence on the NF-κB ex-pression, MVD and AI ( P 〉 0. 05 ). Conclusion Quercetin showed a marked inhibitive effect on U14 growth, and its antitumor mechanism may be associated with inhibiting the angiogenesis and inducing apoptosis.
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