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机构地区:[1]中国医科大学第二临床学院血液研究室,沈阳市110003 [2]中国医科大学第二临床学院细胞生物实验室,沈阳市110003
出 处:《中国肿瘤临床》2004年第5期248-251,共4页Chinese Journal of Clinical Oncology
基 金:国家自然科学基金项目(编号:39470739);卫生部科学研究基金项目(编号:20122167);辽宁省教育厅科研基金项目(编号:202013122)资助
摘 要:目的:探讨TrkA基因通过抑制神经母细胞瘤(NB)血管生成而阻止其生长、转移的可行性。方法:常规培养对照组SY5Y细胞、TrkA基因高表达的实验组细胞(SY5Y-TrkA)和表达载体基因的空载体组细胞(SY5Y-Vec);比较三组细胞的裸鼠皮下致瘤性;通过RT-PCR、免疫组织化学、微血管面积计算检测并比较三种细胞所致的肿瘤瘤体内血管生成情况。结果:SY5Y-TrkA细胞在裸鼠皮下的致瘤性和其所致肿瘤的血管生成能力明显下降。肿瘤终体积:对照组1.736±0.485cm3,空载体组1.803±0.751cm3,实验组0.3945±0.015cm3(P<0.01);对照组与实验组相比,血管内皮生长因子(VEGF)的表达差别显著(P<0.01);微血管密度(MVD):对照组27.21±14.58,空载体组27.76±14.15,实验组4.08±4.72(P<0.01)。结论:TrkA基因能有效抑制神经母细胞瘤的血管生成和肿瘤生长,为应用基因抗血管治疗神经母细胞瘤提供理论依据。Objective: To investigate the feasibility of gene therapy for human neuroblastoma with TrkA gene inhibiting angionenesis. Methods: We cultured regularly the three groups of cells: SY5Y and SY5Y-TrkA and SY5Y-Vec NB cells. The tumorigenesis of the three groups of cells was compared. The tumor volume and angiogenesis of tumors in nude mices was compare and analysed by RT-PCR and immunohistochemistry and microvessel counting. Results: The capability of tumorigenesis and angiogenesis of the TrkA-SY5Y cells in nude mices was greatly reduced. Tumor volume: Control group 1.736(0.485cm3,Empty-Vec group 1.803(0.751cm3,Experiment group 0.3945(0.015cm3 (p(0.01); The distinction of vascular endothelial growth factor(VEGF)expression between experiment group and control group is significant(p(0.01); Microvessel density(MVD): Control group 27.21(14.58,Empty-Vec group 27.76(14.15(, Experiment group 4.08(4.72((p(0.01). Conclusion: The angiogenesis and tumor growth of human neuroblastoma can be effectively inhibited by TrkA gene. This experiment provides a theoretical basis for neuroblastoma angiostatic gene therapy.
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