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纸质出版:2011
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邓雪松,王立.HIF-1α516对人肝癌HepG2细胞侵袭转移能力的影响[J].陆军军医大学学报(原第三军医大学学报),2011,33(02):169-172.
Deng Xuesong,Wang Li.Silencing HIF-1α516 inhibits invasive ability of HepG2 cells[J].J Amry Med Univ (J Third Mil Med Univ),2011,33(02):169-172.
邓雪松,王立.HIF-1α516对人肝癌HepG2细胞侵袭转移能力的影响[J].陆军军医大学学报(原第三军医大学学报),2011,33(02):169-172. DOI:
Deng Xuesong,Wang Li.Silencing HIF-1α516 inhibits invasive ability of HepG2 cells[J].J Amry Med Univ (J Third Mil Med Univ),2011,33(02):169-172. DOI:
目的 观察HIF-1α
516
对人肝癌HepG2细胞侵袭转移能力的影响。 方法 人肝癌HepG2细胞分为空白组(同步培养,不做任何处理)、对照组(转染siRNA)和siRNA干扰组(转染HIF-1α
siRNA)。siRNA和HIF-1α
siRNA通过脂质体转染HepG2,转染18 h 后Western blot 检测HepG2细胞中HIF-1β核蛋白和全细胞蛋白的表达、ELISA法检测细胞培养上清中MMP-2、MMP-9的含量,Transwell小室观察HepG2的转移侵袭能力。 结果 HIF-1α
siRNA能显著降低HepG2细胞HIF-1α
mRNA的表达(降低70.0%)(P0.01);增强HepG2细胞的侵袭转移能力(增强71.10%)(P0.01)。HIF-1α
siRNA对全细胞HIF-1β蛋白的表达无影响,但能促进HIF-1β蛋白的核转移(增强64.1%)(P0.01)。HIF-1α
siRNA能明显升高HepG2细胞培养上清中MMP-2、MMP-9蛋白表达,分别升高37.72%、55.46% (P0.01)。 结论 HIF-1α
能抑制HepG2的转移侵袭,其机制可能与抑制HIF-1β的核转移有关。
Objective To explore the effect of HIF-1α
on invasive ability of HepG2 cells. Methods HepG2 cells were divide into blank group
control group and HIF-1α
siRNA groups
The blank group received no intervention
and the control group and HIF-1α
siRNA group were transfected by siRNA control and HIF-1α
siRNA
respectively with the aid of Liposome. In 18 h later
the effect of HIF-1α
siRNA on HepG2 cells invasive ability in vitro was measured by Boyden chamber invasive models. The expression of HIF-1α
mRNA were measured by real-time PCR. Expression of HIF-1β were detected by Western blot analysis
and the contents of MMP-2 and MMP-9 in the supernatant was measured by ELISA. Results In HIF-1α
siRNA group
the expression of HIF-1α
mRNA were decreased by 70.0%
and contents of MMP-2 and MMP-9 protein were increased by 37.72% and 55.46% (P0. 01)
respectively. The invasive ability of the HIF-1α
siRNA transfected cells was increased by 71.1% (P0.01). HIF-1α
siRNA had no effect on HIF-1β protein expression in HepG2 cells
but it increased the HIF-1β protein expression in HepG2 nucleus by 64.1%(P0.01). Conclusion Silencing HIF-1α
suppresses the invasive ability of HepG2 cells. This may be concerned with that it could inhibit the nuclear transfer of HIF-1β.
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