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Correlative Expression of Glutathion S-Transferase-π and Multidrug Resistance Associated Protein in Bladder Transitional Cell Carcinoma 被引量:7
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作者 杨为民 曾晓勇 +2 位作者 陈春莲 陈忠 杜广辉 《Journal of Huazhong University of Science and Technology(Medical Sciences)》 SCIE CAS 2000年第4期311-314,共4页
In order to elucidate the mechanisms of multidrug resistance (MDR) in bladder cancer, the expression of glutathione S-transferase-π (GST-π) and multidrug resistance associated protein (MRP) in tissue samples resec... In order to elucidate the mechanisms of multidrug resistance (MDR) in bladder cancer, the expression of glutathione S-transferase-π (GST-π) and multidrug resistance associated protein (MRP) in tissue samples resected from 44 patients and 6 normal bladder mucosa as control was de- tected by using immunohistochemical method, and the results were analyzed by computer-assisted im- age analyzing system (IAS) to achieve semi-quantitative data. In addition, correlation between the expression of both factors was studied. The results showed that the positive expression rate of GST- π and MRP in bladder cancer was 72. 7 % (32/44) and 68. 2 % (30/44) respectively, significantly higher than those in normal bladder mucosa, being 16. 7% and 33. 3% respectively. The rate of GST-πpositive staining was increased correspondingly with tumor grade and stage elevated, being higher in recurrent tumors treated by chemotherapy, but not significantly (P>0. 05). There was no significant differences between the expression of MRP and tumors' behaviors and clinical characters. However, the results demonstrated that the correlation between the expression of both resistant fac- tors was very evident (r=0. 695, P<0. 0025). It was suggested that the activation of GST-π and MRP might occur during malignant transformation of normal mucosa, but tumors' differentiation and progression could not be the unique factors that influenced both overexpression. Chemotherapy might be another important reason. The correlation of both indicated that there was a common mech- anism regulating their expression probably, which made them play a pivotal role in chemotherapy drug resistance of bladder cancers. 展开更多
关键词 bladder neoplasm CARCINOMA glutathion S-Transferase-π multidrug resistance as- sociated protein
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姜黄素干预的人结肠癌耐药细胞蛋白质组学分析 被引量:5
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作者 李雷 陈军 +7 位作者 李贺 崔希刚 栾晓鹏 张宇 鲁科翔 曹先圣 毕涛 尹高平 《山东医药》 CAS 2018年第26期18-22,共5页
目的利用蛋白质组学方法,对比经姜黄素处理和未经姜黄素处理的人结肠癌耐药细胞HCT-8/VCR之间差异表达的蛋白,分析与姜黄素逆转结肠癌耐药相关的蛋白。方法取结肠癌耐药细胞HCT-8/VCR,分为观察组和对照组,观察组加入终浓度为25μmol/L... 目的利用蛋白质组学方法,对比经姜黄素处理和未经姜黄素处理的人结肠癌耐药细胞HCT-8/VCR之间差异表达的蛋白,分析与姜黄素逆转结肠癌耐药相关的蛋白。方法取结肠癌耐药细胞HCT-8/VCR,分为观察组和对照组,观察组加入终浓度为25μmol/L的姜黄素作用于人结肠癌耐药细胞HCT-8/VCR 24 h,对照组加入等体积生理盐水。以固相p H梯度等电聚焦为第一向,垂直平板十二烷基磺酸钠聚丙烯酰胺凝胶电泳为第二向(2-DE),分离两组细胞总蛋白;通过凝胶银染显色,扫描仪GS-800采集凝胶图像,图像分析软件PDQuest8.0分析电泳图谱,寻找有意义的差异蛋白点,运用MALDI-TOF-MS系统对选取的蛋白点筛选出差异蛋白并进行质谱鉴定。结果获得了背景清晰、分辨率高、重复性好的HCT-8/VCR细胞2-DE图谱。鉴定出可能与结肠癌多药耐药密切相关的10种蛋白,其中在对照组高表达的有7种,分别是谷胱甘肽S转移酶P1(GSTP1)、重组人FK506结合蛋白4(FKBP4)、X线修复交叉互补基因5(XRCC5)、肿瘤蛋白翻译调节因子1(TPT1)、热休克蛋白8(HSPA8)、超氧化物歧化酶1(SOD1)、前列腺特异性膜抗原剪接变体(PSMA5);在观察组中高表达的有3种,分别是肽基脯氨酰顺反异构酶(PPIB)、鸟氨酸转氨酶(OAT)、核内不均一核糖核蛋白H1(HNRNPH1)。结论姜黄素干预HCT-8/VCR后出现10种差异性表达的蛋白,蛋白功能涉及信号传导、肿瘤细胞的分裂、多药耐药以及抗氧化、凋亡和糖酵解等,可能与姜黄素逆转HCT-8/VCR细胞对化疗药物的耐药性有关。 展开更多
关键词 结肠肿瘤 姜黄素 蛋白质组学 双向凝胶电泳 多药耐药相关蛋白质
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在体单向肠灌流模型研究千金子甾醇在大鼠肠吸收特性 被引量:3
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作者 张秀婷 王英姿 +6 位作者 李韶菁 段飞鹏 王晴 张春泥 李凤英 李文华 骆声秀 《北京中医药大学学报》 CAS CSCD 北大核心 2015年第9期624-627,共4页
目的研究千金子甾醇在大鼠肠道内的吸收情况以及P-糖蛋白(P-gp)和多药耐药相关蛋白(MRP2)对千金子甾醇肠吸收的影响。方法采用大鼠在体单向肠灌流模型,运用高效液相色谱法测定十二指肠、空肠、回肠、结肠灌流液中千金子甾醇的含量,计算... 目的研究千金子甾醇在大鼠肠道内的吸收情况以及P-糖蛋白(P-gp)和多药耐药相关蛋白(MRP2)对千金子甾醇肠吸收的影响。方法采用大鼠在体单向肠灌流模型,运用高效液相色谱法测定十二指肠、空肠、回肠、结肠灌流液中千金子甾醇的含量,计算吸收速率常数(Ka)和表观渗透系数(Papp)。结果千金子甾醇在大鼠结肠的Ka及Papp最高(P<0.05)。加入P-gp抑制剂盐酸维拉帕米后,千金子甾醇在结肠段的Ka及Papp显著增加;而加入MRP2抑制剂吲哚美辛后,千金子甾醇在大鼠结肠段的Ka及Papp普遍降低。结论千金子甾醇在肠道中的主要吸收部位为结肠,推测千金子甾醇可能为P-gp的底物,而非MRP2的底物。 展开更多
关键词 单向肠灌流 千金子甾醇 P-糖蛋白 多药耐药相关蛋白 大鼠
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