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脾源性酪氨酸激酶Syk的抗肿瘤作用

Anti-Tumor Effect of Spleen Tyrosine Kinase

  • 摘要: 目的探讨脾源性酪氨酸激酶(spleen tyrosine kinase,Syk)的体内外抗肿瘤作用。方法经脂质体介导将全长Syk cDNA转入Syk阴性表达的高侵袭性人乳腺癌细胞株MDA-MB-231,应用MTT法、Transwell小室法分别检测SykcDNA体外抗肿瘤细胞增殖及侵袭迁移作用;采用BABL/c(nu/nu)裸鼠皮下移植瘤模型,检测转染及未转染肿瘤细胞的成瘤及肺转移情况。结果转染全长Syk cDNA的MDA—MB-231细胞与转染空载体及未转染MDA—MB-231细胞相比,体外增殖情况未见明显改变,而侵袭及迁移实验中的穿膜细胞数(总迁移细胞数/5HPF)却均明显减少(P〈0.05);同样,接种不同肿瘤细胞的裸鼠皮下移植瘤成瘤情况未见明显差异,但接种转染组肿瘤细胞的肺转移率却显著低于未转染组及空载体转染组(P〈0.05)。结论Syk通过改变乳腺肿瘤细胞的侵袭迁移能力参与其抗瘤作用。

     

    Abstract: Objective  To investigate the anti2tumor effect of spleen tyrosine kinase (Syk) in vit ro and in vi vo. Methods  Human breast cancer cell line MDA2MB2231 which expressing Syk negatively was cul2 tured in optimum medium and t ransfected with Syk cDNA by liposome, and cells t ransfected with blank vector were used as cont rol. The inhibited effect of Syk cDNA on the cell proliferation and the ability of assorting in vit ro was detected by MTT and Transwell2ECM methode ; the pulmonary metastasis and tumor growth of t ransformed and unt ransformed human breast cancer cells were investigated by xeno2 graf t s in BABL/ c (nu/ nu) athymic mice. Results  There is no obviously change in proliferation in vit ro, between the MDA2MB2231 cells t ransformed Syk cDNA and t ransformed idling or not t ransformed, but number of the migrating cells (migrating cells/ 5 HPF) reduces obviously in invasion and immigration ex2 periment ( P < 0. 05) ; in the same, there is no difference in tumor growth of athymic mice inoculated dif2 ferent cancer cells, nevertheless, there is lower incidence of pulmonary metastasis in the group of inocula2 ted cancer cells t ransforming Syk cDNA ( P < 0. 05) . Conclusion  Syk can rest rain in tumor by reducing the abilities of invasion and migration of breast cancer cells.

     

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