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脂质体-c-raf-1 反义寡核苷酸转染对人卵巢癌裸鼠皮下移植瘤形成的作用[J]. 肿瘤防治研究, 2005, 32(03): 149-151. DOI: 10.3971/j.issn.1000-8578.2462
引用本文: 脂质体-c-raf-1 反义寡核苷酸转染对人卵巢癌裸鼠皮下移植瘤形成的作用[J]. 肿瘤防治研究, 2005, 32(03): 149-151. DOI: 10.3971/j.issn.1000-8578.2462
Effects of Liposome-c-raf-1 Antisense Oligodeoxynucleotides Transfection on the HumanOvarian Cancer Transplanted Subcutaneously in Nude Mice[J]. Cancer Research on Prevention and Treatment, 2005, 32(03): 149-151. DOI: 10.3971/j.issn.1000-8578.2462
Citation: Effects of Liposome-c-raf-1 Antisense Oligodeoxynucleotides Transfection on the HumanOvarian Cancer Transplanted Subcutaneously in Nude Mice[J]. Cancer Research on Prevention and Treatment, 2005, 32(03): 149-151. DOI: 10.3971/j.issn.1000-8578.2462

脂质体-c-raf-1 反义寡核苷酸转染对人卵巢癌裸鼠皮下移植瘤形成的作用

Effects of Liposome-c-raf-1 Antisense Oligodeoxynucleotides Transfection on the HumanOvarian Cancer Transplanted Subcutaneously in Nude Mice

  • 摘要: 目的 探讨经脂质体一硫代磷酸化修饰的c-raf-1反义寡脱氧核苷酸(ASODN)作用后的卵巢上皮癌细胞株SKOV3在裸鼠皮下的成瘤能力。方法 利用脂质体将经硫代磷酸化修饰的寡核苷酸导入SKOV3细胞,然后将这种被转染的细胞接种于裸鼠皮下,观察肿瘤体积的变化,并计算抑瘤率。结果 经脂质体c-raf-1 ASODN作用后的卵巢上皮癌细胞在裸鼠皮下成瘤能力降低,最大抑瘤率达35.3%(P<0.05)。首次出现肉眼可见肿瘤的平均时间延长为8.8天(P<0.05)。结论 c-raf-1癌基因的反义调控能降低卵巢上皮癌细胞的成瘤能力,抑制肿瘤生长,在卵巢上皮癌的基因治疗中有一定作用。

     

    Abstract: Objective  To investigate the effect s of liposome-c-raf-1 antisense phosphoro-thioate oligodeoxy-nucleotides (c-raf-1 ASODN) on the human ovarian epithelial cancer t ransplanted subcutaneously in nude mice. Methods  Human ovarian epithelial cancer cell lines SKOV3 were t reated with liposome-c-raf-1 ASODN, then transplanted subcutaneously in nude mice. The Changes of tumor volume were observed and the tumor growth inhibitory rate was calculated. Results  The tumorigenic ability of the t reated cell lines was reduced, the maximum tumor growth inhibitory rate was 35. 3 %( P < 0. 05) . The first time that tumor can be detected was increased up to 8. 8 days ( P < 0. 05) . Conclusion  The results suggested that c-raf-1 ASODN transfection can inhibit the tumorigenesis of ovarian epithelial cancer cell lines in nude mice, it may be a useful gene therapy for the ovarian epithelial carcinoma.

     

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