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首页|期刊导航|中山大学学报(医学科学版)|VEGF-C调节miR-145/SIP1增强宫颈癌细胞侵袭能力

VEGF-C调节miR-145/SIP1增强宫颈癌细胞侵袭能力

程杨 顾正田

中山大学学报(医学科学版)2018,Vol.39Issue(2):215-219,5.
中山大学学报(医学科学版)2018,Vol.39Issue(2):215-219,5.

VEGF-C调节miR-145/SIP1增强宫颈癌细胞侵袭能力

VEGF-C Promotes Cervical Cancer Invasion via Regulation of microRNA-145/Smad Interacting Protein 1

程杨 1顾正田1

作者信息

  • 1. 广州市第一人民医院妇产科,广东广州510180
  • 折叠

摘要

Abstract

[Objective]To investigate the role of microRNA-145/Smad interacting protein 1(SIP 1)in VEGF-C-enhanced cervical cancer metastasis.[Methods]Cervical cancer cell line SiHa cells were cultured and treated with VEGF-C to observe its effect on the expression of miR-145 and SIP1. After transfection with specific SIP1 siRNA,the invasion number of cultured cells were calculated by transwell chamber assay.[Results]Treatment with VEGF-C(100 ng/mL)for 12 h,24 h and 48 h all reduced miR-145 expression,with the expression abundance of(82.4±6.4)% (P<0.05),(72.5±7.2)%(P<0.01),and(60.6±9.6)%(P<0.001),respectively,when compared to control.Meanwhile, the same treatment with VEGF-C also increased SIP1 protein expression,with the expression abundance of(142.4 ± 16.5)%(P<0.05),(183.6 ± 11.4)%(P<0.01)and(220.8 ± 15.7)%(P<0.001),respectively. The transfection of miR-145 mimic significantly impaired VEGF-C effect on SIP1 expression. Finally,VEGF-C promoted SiHa cell invasion,which was largely inhibited by the tranfection of SIP siRNA with the inhibitory rate of(56.6±10.3)%(P<0.01).[Conclusion]VEGF-C downregulates miR-145,thus increases SIP1 expression and promotes cervical cancer cell invasion,which may contributes to cervical cancer malignant progression.

关键词

宫颈癌/血管内皮生长因子C/microRNA-145/Smad相互作用蛋白1/侵袭

Key words

cervical cancer/vascular endothelial growth factor C/microRNA-145/Smad interacting protein 1/invasion

分类

医药卫生

引用本文复制引用

程杨,顾正田..VEGF-C调节miR-145/SIP1增强宫颈癌细胞侵袭能力[J].中山大学学报(医学科学版),2018,39(2):215-219,5.

基金项目

广东省医学科研基金(A2015058),广州市科技计划项目(2014J4100113),广东省科技计划项目(2013B021800068) (A2015058)

中山大学学报(医学科学版)

OA北大核心CSCDCSTPCD

1672-3554

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