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Yangfei Kongliu Formula, a compound Chinese herbal medicine, combined with cisplatin, inhibits growth of lung cancer cells through transforming growth factor-β1 signaling pathway 被引量:4
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作者 Shui-jie Shen Yong-hong Zhang +2 位作者 Xiao-xia Gu Shui-ju Jiang Ling-jun Xu 《Journal of Integrative Medicine》 SCIE CAS CSCD 2017年第3期242-251,共10页
OBJECTIVE: To investigate the tumor inhibition effect of Yangfei Kongliu Formula (YKF), a compound Chinese herbal medicine, combined with cisplatin (DDP) and its action mechanisms. METHODS: C57BL/6 mice with Lew... OBJECTIVE: To investigate the tumor inhibition effect of Yangfei Kongliu Formula (YKF), a compound Chinese herbal medicine, combined with cisplatin (DDP) and its action mechanisms. METHODS: C57BL/6 mice with Lewis lung carcinoma were divided into six groups: control group (C), DDP group (2 mg/kg, DDP), low-dose YKF group (2.43 g/kg, L), high-dose YKF group (24.3 g/kg, H), low- dose YKF combined with DDP group (L + DDP) and high-dose YKF combined with DDP group (H + DDP). Transforming growth factor-β1 (TGF-β1), mothers against decapentaplegic homolog 3 (Smad3) and Smad7 levels were measured with quantitative real-time polymerase chain reaction (qPCR), Western blotting and immunohistochemistry. An enzyme-linked immunosorbent assay was used to analyze the expressions of interleukin-2 (IL-2) and tumor necrosis factor-α (TNF-α). RESULTS: YKF combined with DDP significantly inhibited the growth and metastasis of tumors relative to the control group, and YKF groups (P 〈 0.05). There was no significant difference between high-dose YKF group and low-dose YKF group (P 〉 0.05). We also found that the expression levels of TGF-β1 and Smad3 were both significantly decreased by YKF relative to the control group (P 〈 0.05). Furthermore, after treatment with YKF combined with DDP, the expression levels of TGF-β1 and Smad3 were decreased but the expression level of Smad7 was increased relative to the DDP group (P 〈 0.05). Compared to the DDP group, the combination of YKF and DDP enhanced the effect of tumor inhibition (P 〈 0.05), showing obvious synergy between YKF and DDP. Treatment with DDP or YKF decreased serum levels of IL-2 and TNF-α relative to the control group (P 〈 0.05). Furthermore, the expression levels of IL-2 and TNF-α were significantly decreased when treated with YKF in combination with DDP. Co-treatment with YKF and DDP significantly inhibited tumor growth, decreased the expressions of TGF-β1, Smad3, IL-2 and TNF-α and increased the expression of Smad7; these differences were significant relative to both YKF groups and the control group (P 〈 0.05). CONCLUSION: YKF can inhibit tumor growth synergistically with DDP, mainly through the TGF-β1 signaling pathway. 展开更多
关键词 CISPLATIN transforming growth factor-β1 SMAD3 SMAD7 lung cancer drugs chinese herbal
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伤科接骨片对实验型骨折愈合过程中TGF-β_1的影响 被引量:16
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作者 石关桐 吴宇峰 +1 位作者 沈培芝 曹月龙 《中国骨伤》 CAS 2001年第12期727-729,共3页
目的 观察应用伤科接骨片后骨折愈合过程中TGF β1(转化生长因子 β1)的变化 ,以进一步探讨其促进骨折愈合的机理。方法  72只日本大耳白兔随机分为实验组和对照组 ,每组各 36只。在兔桡骨处用手术方法制备骨折模型 ,术后即日起试验... 目的 观察应用伤科接骨片后骨折愈合过程中TGF β1(转化生长因子 β1)的变化 ,以进一步探讨其促进骨折愈合的机理。方法  72只日本大耳白兔随机分为实验组和对照组 ,每组各 36只。在兔桡骨处用手术方法制备骨折模型 ,术后即日起试验组给与伤科接骨片 ,15 0mg/kg/d。于术后 3天、1周、2周、3周、4周、6周每组分别处死 6只兔 ,取标本 ,采用免疫组化方法进行染色 ,光镜下观察 ,并利用图像分析的方法测定其TGF β1表达强度。结果 在骨折后的同一时间 ,实验组和对照组的骨痂组织中TGF β1的染色有差异 ,实验组的峰值比对照组约提前一周出现 ,且比对照组的峰值高。结论 伤科接骨片可以调节骨折愈合过程中TGF β1的合成和分泌 ,从而促进骨折的愈合。TGF β1可能是伤科接骨片对骨折愈合过程影响的一个作用环节。 展开更多
关键词 中成药 骨折 转化生长因子Β
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参麦液对早期退变腰椎间盘组织中NO、TGF-β_1表达的影响 被引量:3
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作者 林定坤 郭玉海 +4 位作者 陈博来 孔畅 杨仁轩 赵帅 黄刚 《中国骨伤》 CAS 2005年第3期142-143,共2页
目的:探讨参麦液在延缓椎间盘退变中的作用。方法:对6例年轻腰椎间盘突出患者的椎间盘组织采取体外细胞培养,随机分为4组:对照组、1%参麦液组、2 . 5 %参麦液组、5 %参麦液组,用分光光度法测定各组培养上清液中NO含量与NOS活性,并采用... 目的:探讨参麦液在延缓椎间盘退变中的作用。方法:对6例年轻腰椎间盘突出患者的椎间盘组织采取体外细胞培养,随机分为4组:对照组、1%参麦液组、2 . 5 %参麦液组、5 %参麦液组,用分光光度法测定各组培养上清液中NO含量与NOS活性,并采用免疫组化的研究方法测定椎间盘细胞TGF β1表达。结果:对照组退变椎间盘组织产生的NO为(14 4. 1±9 .7) μmol/L ,NOS为(6 . 2±0 .6 )U/ml,高于参麦液组,有统计学差异。参麦液组中的椎间盘细胞呈不同程度的棕黄色,对照组则呈阴性改变。结论:参麦液可降低椎间盘内炎症因子的浓度,促进椎间盘细胞TGF -β1表达,有效减缓椎间盘组织的退变。 展开更多
关键词 TGF-β1表达 参麦液 腰椎间盘组织 早期退变 椎间盘细胞 体外细胞培养 腰椎间盘突出 椎间盘退变 NOS活性 培养上清液 分光光度法 mol/L 统计学差异 对照组 NO含量 免疫组化 不同程度 炎症因子 椎间盘内 棕黄色 测定
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