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垂体瘤转化基因反义寡核苷酸抑制胶质瘤增殖的实验研究 预览 被引量:3

Antisense oligodeoxyribonucleotide of pituitary tumor transforming gene inhibits proliferation of glioblastoma
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摘要 目的观察垂体瘤转化基因(pituitary tumor transforming gene,PTrG)反义寡核苷酸(antisense oligodeoxynucleotide,ASODN)对恶性胶质瘤增殖的抑制作用。方法将c6胶质瘤细胞接种于大鼠右侧尾状核。按照不同的PTTG反义寡核苷酸浓度在选定的时间点立体定向原位注射于肿瘤区域。3周后处死大鼠,取标本做GFAP、PTTG、PCNA免疫组化染色。结果不同浓度的PTTG-ASODN对C6胶质瘤模型的增殖抑制呈时间、浓度依赖性,而且高浓度,早期应用,反复应用PTTG-ASODN抑制胶质瘤模型肿瘤增殖的效果明显。结论PTTG-ASODN可以抑制胶质瘤的增殖,有望成为胶质瘤基因治疗的一种新策略。 Objective To investigate the inhibition effect of pituitary tumor transforming gene (PTTG) antisense oligodeoxynucleotide (ASODN) on C6 glioblastoma in rats. Methods The C6 glioma cells were injec- ted into the right caudate nucleus. PTTG-ASODN of 8 or 16 μg/ml was injected into the tumor-affected area with stereotactic technique immediately, at 1st and 2rid week after inoculation of C6 cells. Three weeks after C6 cell inoculation, all rats were killed and the tumors were excised, then tumor volume was calculated and pathologically analysed, and immunohistochemical statining for GFAP, PCNA ang PTTG was performed. Results PTTG-ASODN could suppress the proliferation of C6 glioblastoma in a dose- and time-dependent manner. The inhibition effect was better when large-dose PTTG-ASODN was repeatedly used for glioblastoma as early as possible. Conclusion PTTG-ASODN can suppress the proliferation of glioblastoma, which may become a new strategy of gene therapy for glioblastoma.
作者 程迎新 高原 唐文渊 陈丙波 CHENG Ying-xin , GAO Yuan, TANG Wen-yuan , CHEN Bing-bo ( 1 Department of Neurosurgery, 2 Department of Gerontology, The First Affiliated Hospital, Chongqing University of Medical Sciences, Chongqing 400016; 3 Laboratory Animal Center, Third Military Medical University, Chongqing 400038, China)
出处 《第三军医大学学报》 CAS CSCD 北大核心 2006年第19期 1962-1964,共3页 Acta Academiae Medicinae Militaris Tertiae
关键词 胶质瘤 垂体瘤转化基因 反义寡核苷酸 glioblastoma pituitary tumor transforming gene ASODN
作者简介 程迎新(1977-),男,山东省潍坊市人,博士,主要从事脑胶质瘤基础方面的研究。电话:13206172038,E-mail:cqykdx@hotmail.com 通讯作者:唐文渊,电话:(023)89011159
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参考文献6

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二级参考文献8

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