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磁性载药微球联合反义寡核苷酸对人胰腺癌裸鼠模型的疗效观察
引用本文:赵会庚,权广前,潘耀振,尹家俊. 磁性载药微球联合反义寡核苷酸对人胰腺癌裸鼠模型的疗效观察[J]. 实用癌症杂志, 2017, 0(2): 181-184. DOI: 10.3969/j.issn.1001-5930.2017.02.003
作者姓名:赵会庚  权广前  潘耀振  尹家俊
作者单位:1116001,大连大学附属中山医院
基金项目:辽宁省自然科学基金(201102006)
摘    要:目的 探讨辐射促细胞转染的多药耐药(multidrug resistance,MDR)基因mdr1反义寡核苷酸(ASON)联合5-氟尿嘧啶磁性载药微球(PEG-5-FU-MAMS)治疗裸鼠人胰腺癌的效果.方法 通过构建裸鼠人胰腺癌耐药肿瘤模型基础上,肿瘤局部以2 Gy60 Coγ辐射,瘤内注射阳性脂质体介导的mdr1反义寡核苷酸(ASON),经磁导下利用磁性载药微球(PEG-5-MAMS)联合化疗.结果 联合辐射组与未联合辐射组及对照组肿瘤生长曲线肿瘤生长曲线差异有显著性(P<0.01).联合组能显著抑制肿瘤的生长,联合组肿瘤重量抑制率为85.00%,肿瘤体积抑制率为87.74%.结论 辐射促转染的mdr1ASON联合磁性载药微球对肿瘤细胞具有较好的耐药逆转作用.

关 键 词:电离辐射  反义寡核苷酸  转染  多药耐药  PEG-5-FU-MAMS

Reversal of Multidrug Resistance Antisense Oligodeoxynucletedes and PEG-5-FU-MAMS for Human Pancreatic Carcinoma Model in Nude Mice
Abstract:Objective To investigate the efficacy of reversal of multidrug resisitance ( MDR) by MDR gene mdrl anti-sense oligodeoxynucletdes (ASON) and Polyethylene Glycol modified 5-Fluorouracil magnetic albumin miscrospheres (PEG-5-FU-MAMS) for the human pancreatic cancer cell line in SW 1990/Fu,and realize magnetic targeted therapy the human pancreatic cancer in nude mouse model .Methods dr1 ASON was injected into the tumor 1 hour after local 2 Gy60 Coγirradition.The tumor-suppressing rate and tumor-suppressing curve were observed in the 2 groups of cells after treatment with Polyethylene Glycol modified 5-Fluorouracil magnetic albumin miscrospheres (PEG-5-FU-MAMS).Results Significant differences in tumor weight and tumor volume were also observed between the 2 different treat group(P<0.01).The suppressing rates of tumor volume and weight were 87.74%and 85.00%respectively in grouop accepted combined radiation .Conclusion The reversal effect of mdr1 ASON and ionizing radiation plus Polyethy-lene Glycol modified 5-Fluorouracil magnetic albumin miscrospheres ( PEG-5-FU-MAMS) is stronger on resistant cell than that of mdr 1 ASON and Polyethylene Glycol modified 5-Fluorouracil magnetic albumin miscrospheres(PEG-5-FU-MAMS) alone.
Keywords:Ionizing radition  Antisense Oligodeoxynuce-letides  Gene transfection  Multidrug resistance  PEG-5-FU-MAMS
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