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Effects of Chinese Jianpi herbs on cell apoptosis and related gene expression in human gastric cancer grafted onto nude mice

机译:健脾中药对裸鼠人胃癌细胞凋亡及相关基因表达的影响

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摘要

AIM: To explore the mechanism of the Sijunzi decoction and another Chinese herbal recipe (SRRS) based mainly on the Sijunzi decoction in treatment of gastric cancer.METHODS: A human gastric adenocarcinoma cell line SGC-7901 grafted onto nude mouse was used as the animal model. The mice were divided into 3 groups, one control and the two representative experimental conditions. Animals in the two experimental groups received either Sijunzi decoction or SRRS over a 40-day period starting at 1st day after grafting. Control animals received saline on an identical schedule. Animals were killed 41 d after being grafted. The effect of therapy was assessed by two ways: (1) tumor size was periodically measured during the life of the animals; (2) tumor weight was determined by a electron balance immediately after the animals killed. For detection of apoptotic cells, apoptotic indices (AI) were examined by the terminal deoxynucleotidyl transferase-mediated deoxyuridine triphosphate fluorescence nick end labeling (TUNEL) method. Morphological alterations were observed with electron microscopy. S-P immunohistochemical method was used to detect the expression of Ki-67 in xenografts. Expression of bcl-2 and p53 was semiquantitatively detected using a reverse transcriptase-polymerase chain reaction (RT-PCR) technique.RESULTS: When compared with controls, tumor growth (size and weight) was significantly inhibited by treatment with the Sijunzi decoction (P < 0.05) or SRRS (P < 0.01). The tumor inhibitory rate in the Sijunzi decoction group was 34.33% and SRRS group 46.53%. AI of human gastric cancer xenografts in nude mice was significantly increased to 16.24% ± 3.21% using TUNEL method and 11.38% ± 6.46% by FACScan in the Sijunzi decoction group compared with the controls (TUNEL: 2.63% ± 1.03%, P < 0.01; FACScan: 7.15% ± 1.32%, P < 0.05). SRRS group was also found a significantly increased AI by using TUNEL method and flow cytometry analysis compared with the controls (TUNEL: 13.18% ± 3.05%, P < 0.05; FACScan: 11.58% ± 5.71% (P < 0.05). Under electron microscope, cell shrinkage, nuclear chromatin condensation, formation of membrane blebs and apoptotic bodies were frequently observed in Sijunzi decoction group and SRRS group. The average labeling index (LI) for Ki-67 in SRRS group was significantly decreased to 8.43% ± 2.22% compared with the control group (10.37% ± 4.91%) (P < 0.05). The average labeling index for Ki-67 in sijunzi decoction group was 7.95% ± 2.54% which was lower than that of the control group, but showed no significance (P = 0.07). The expression level of p53 mRNA was lower in both Sijunzi decoction group and SRRS group than that in control group (P < 0.05; P < 0.01). The expression of bcl-2 mRNA was also decreased in SRRS group compared with the control (P < 0.01).CONCLUSION: The inhibition of gastric cancer cell growth in vivo by Chinese Jianpi herbs and SRRS is related to induction of the cell apoptosis which may be involved in aberrant expression of p53 and bcl-2 genes.
机译:目的:探讨四君子汤和另一种以四君子汤为主要成分的中草药配方治疗胃癌的机理。方法:以裸鼠移植人胃腺癌细胞SGC-7901为动物。模型。将小鼠分为3组,一组为对照组,两组为代表性实验条件。两个实验组的动物在移植后第一天开始的40天内接受了四君子汤或SRRS。对照动物以相同的时间表接受盐水。移植41天后将动物处死。通过两种方法评估治疗效果:(1)在动物的生命周期中定期测量肿瘤大小; (2)杀死动物后立即通过电子平衡确定肿瘤重量。为了检测凋亡细胞,通过末端脱氧核苷酸转移酶介导的脱氧尿苷三磷酸荧光缺口末端标记(TUNEL)方法检查了凋亡指数(AI)。用电子显微镜观察形态变化。采用S-P免疫组化方法检测Ki-67在异种移植物中的表达。结果:与对照组相比,四君子汤(P组)显着抑制了肿瘤的生长(大小和重量),与对照相比,bcl-2和p53的表达被半定量检测。 <0.05)或SRRS(P <0.01)。四君子汤组肿瘤抑制率为34.33%,SRRS组为46.53%。与对照相比,四君子汤组的裸鼠人胃癌异种移植物的AI通过TUNEL法显着提高至16.24%±3.21%,通过FACScan显着提高至11.38%±6.46%(TUNEL:2.63%±1.03%,P <0.01 ; FACScan:7.15%±1.32%,P <0.05)。 SRRS组通过TUNEL法和流式细胞术分析也发现AI明显高于对照组(TUNEL:13.18%±3.05%,P <0.05; FACScan:11.58%±5.71%(P <0.05)。在四君子汤组和SRRS组中经常观察到细胞收缩,核染色质浓缩,膜泡和凋亡小体的形成,SRRS组中Ki-67的平均标记指数(LI)显着降低至8.43%±2.22%与对照组相比(10.37%±4.91%)(P <0.05)。四君子汤组Ki-67的平均标记指数为7.95%±2.54%,低于对照组,但无统计学意义( P = 0.07)。四君子汤组和SRRS组的p53 mRNA表达水平均低于对照组(P <0.05; P <0.01); SRRS组的bcl-2 mRNA表达也降低。结论:胃癌的抑制作用与对照组相比差异有统计学意义(P <0.01)。健脾中药和SRRS在体内癌细胞的生长与细胞凋亡的诱导有关,其可能与p53和bcl-2基因的异常表达有关。

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