siRNA沉默VEGF-C基因对宫颈癌HeLa细胞的生物学特性影响  被引量:4

Effect of Molecular Biology of Inhibition of VEGF-C in HeLa Cell Lines by siRNA in Vitro

在线阅读下载全文

作  者:陈星[1] 王美芬[1] 吴朝阳[1] 郑灵芝[1] 任虹平[1] 郑曙民[2] 熊冬生[3] 杨纯正[3] 糜若然[4] 

机构地区:[1]温州医学院附属浙江省台州医院妇产科,317000 [2]山西省肿瘤医院,太原030001 [3]中国医学科学院北京协和医学院血液学研究所,300520 [4]天津医科大学总医院,300520

出  处:《医学研究杂志》2011年第11期58-62,共5页Journal of Medical Research

基  金:浙江省卫生厅科技基金资助项目(2008196B);浙江省台州科技基金课题(08YK14)

摘  要:目的通过RNA干扰技术抑制宫颈癌细胞VEGF-C表达,探讨干扰后VEGF-C、NF-κB、bcl-2基因的表达。方法根据人VEGF-C mRNA编码序列,设计RNA干扰的靶点,并用脂质体转染人宫颈癌HeLa细胞,通过RT-PCR法观察转染后肿瘤细胞VEGF-C、NF-κB、bcl-2基因的变化。结果转染siRNA 24h、48h可以使HeLa细胞VEGF-C mRNA含量降低,在24h降低80.63%±0.24%(P<0.001);在48h降低38.9%±0.85%(P<0.01);NF-κB mRNA含量也分别降低,在24h降低37.55±2.76%(P<0.05);在48h降低30.5%±3.82%(P=0.056);bcl-2mRNA含量同时分别降低,在24h降低76.95%±1.91%,(P<0.01);在48h降低64.11%±2.96%,(P<0.05))。结论脂质体介导的VEGF-C siRNA转染HeLa细胞后,可以有效抑制VEGF-C的表达;可能通过下调转录因子NF-κB,抑制抗凋亡基因bcl-2的表达。Objective To analysis the expression of VEGF - C,NF - KB,bcl - 2 gene by inhibiting VEGF - C expression of tumor cells with RNA interference (RNAi) technique. Methods According to the encoding sequence mRNA of human VEGF - C,the target site for RNAi was designed, siRNA was transfected by liposome and the expression of VEGF - C, NF - KB, bcl - 2 mRNA was further observed by RT - PCR. Results The expression of VEGF - C of HeLa cell lines treated with siRNA for 24h,48h was significantly inhibited,with in24hSO. 63% ±0.24% (P〈O.O01) and in48h38.9% +0.85%(P〈0. O1).The expression of NF-KB was also down-regulated in 24h,48h,with in 24h 37.55% + 2.76% (P 〈0.05) and in 48h 30.5% ±3.82% (P =0. 056). Thus the expression of bcl - 2 was also inhibited in 24h,48h,with in 24h 76. 95%±1 .91% (P〈0.01) and in 48h 64. 11% +2.96% (P〈0.05).Conclusion After being treated with VEGF - C siRNA of the HeLa cells, the expression of VEGF - C is effectively inhibited, NF - KB may be down - regulated and anti - apoptosis bcl - 2 gene is effectively inhibited.

关 键 词:血管内皮生长因子-C BCL-2 NF-ΚB 宫颈癌 RNA干扰 

分 类 号:R284.1[医药卫生—中药学]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象