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作 者:高军[1] 苏琳 王淑云[1] 王亮 张建立[1] 谭晓杰[1]
机构地区:[1]青岛大学医学院附属医院普外科,266000 [2]淄博市淄川区医院内科
出 处:《中华实验外科杂志》2010年第11期1681-1683,F0004,共4页Chinese Journal of Experimental Surgery
基 金:山东省自然科学基金资助项目(Y2007C030)
摘 要:目的 观察β1整合素表达下调对人结肠癌HT-29细胞侵袭和耐药的影响.方法 反义寡核苷酸技术转染HT-29细胞,逆转录-聚合酶链反应(RT-PCR)检测β1整合素表达下凋.Transwell侵袭窒方法检测HT-29体外侵袭力.流式细胞术(FCM)和噻唑蓝(MTT)比色法检测不同剂量的化疗药物[5-氟尿嘧啶(5-Fu)]对各组凋亡率和生长抑制率的影响.结果 实验组HT-29细胞βl整合素mRNA表达显著降低,体外侵袭实验迁移的HT-29细胞数(59±12)明显减少(P<0.05),在高浓度5-Fu(100、200 mg/L)时HT-29细胞的生长抑制率(36.97%和47.58%)和细胞凋亡率[(15.7l±1.46)%、(27.82±1.58)%]与对照组比较差异有统计学意义(P<0.05).结论 β1整合素表达下调可降低结肠癌细胞侵袭及化疗药物耐药性.Objective To investigate the effects of down-regulation of integrin-β1 expression on cell invasion and chemotherapy-resistance of human colon carcinoma cell line HT-29. Methods The down-regulation of integrin-β1 mRNA expression by antisense oligonucleotide technologies was determined with reverse transcription-polymerase chain reaction (RT-PCR). The invasive ability in vitro was evaluated by Transwell invasion chamber assay. Growth inhibition rates and apoptosis rates of HT-29 cells under different dosages of chemotherapeutic agents [5-fluorouracil (5-Fu)] were measured by methyl thiazol tetrazolium (MTT) colorimetric assay and flow cytometry (FCM). Results In contrast with control group,the expression of integrin-β1 mRNA of HT-29 cells were markedly down-regulated,and the number (59 ±12) of migrated HT-29 cells was significantly decreased in the experimental group (P 〈 0. 05 ). Higher dosages ( 100 mg/L and 200 mg/L of 5-Fu) caused a greater increase of inhibition in experimental group than in control ( P 〈 0. 05 ). Conclusion The results demonstrate that down-regulation of integrin-β1 expression can effectively decrease cell invasion and chemotherapy-resistance of human colon carcinoma cell line HT-29.
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