The reinforcement of invasion in epithelial ovarian cancer cells by 17β-estradiol is associated with up-regulation of Snail

被引:46
作者
Ding, Jing-Xin
Feng, You-Ji
Yao, Liang-Qing
Yu, Min
Jin, Hong-Yan
Yin, Lian-Hua
机构
[1] Fudan Univ, Shanghai Med Coll, Dept Gynecol & Obstet, Gynecol & Obstet Hosp, Shanghai 200011, Peoples R China
[2] Cold Spring Harbor Lab, Cold Spring Harbor, NY 11724 USA
[3] Fudan Univ, Shanghai Med Coll, Dept Pathol Physiol, Shanghai 200032, Peoples R China
关键词
estrogens; epithelial ovarian cancer; Snail; siRNA expression vector; matrix metalloproteinase-2; E-cadherin;
D O I
10.1016/j.ygyno.2006.04.023
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective. The transcription factor Snail, which is implicated in the triggering of epithelial-mesenchymal transitions (EMT), plays an important role in adhesion, invasion and metastasis of tumor cells. In the present study, we assessed 17 beta-Estradiol (E-2)'s effect on Snail, E-cadherin and MMP-2 expression of epithelial ovarian cancer cell line ES-2 and SKOV3. Then we induced Snail gene silencing by RNA interference to explore the effect of E-2 on E-cadherin and MMP-2 expression when Snail gene expression was blocked. Methods. Treated by 10(-8) M E-2, Snail, E-cadherin and MMP-2 mRNA expression of the cells was measured by RT-PCR; Snail, MMP-2 protein expression was detected by IHC; and MMP-2 activity was determined by Zymography. E-cadherin protein level was measured by Western blot. We constructed the small interfering dsRNA expression vector (pRNAT-U6.1/Neo-Snail) targeting Snail gene, as well as a negative control vector (pRNAT-U6.1/Neo-Neg). Then the cells were transiently transfected with the vectors. Western blot and zymography were conducted to determine E-cadherin protein level and matrix metalloproteinase activity of the cells transfected with pRNAT-U6.1/Neo-Snail or pRNAT-U6.1/Neo-Neg after treated with E-2 for 24 h. Results. The expression of ER alpha mRNA and protein was negative in ES-2 cells and positive in SKOV3 cells, and ER beta expression was positive in both cell lines. 10(-8) mol/l E-2 elevated expression of Snail and MMP-2 mRNA and protein in both ES-2 and SKOV3 cells, and reduced expression of E-cadherin mRNA and protein in SKOV3 cells. While in the RNAi group transfected with the small interfering dsRNA expression vector (pRNAT-U6.1/Neo-Snail) targeting Snail gene, E-2 treatment did not have a significant effect on MMP-2 activity or E-cadherin protein in ES-2 and SKOV3 cells. Conclusions. 17 beta-Estradiol increased Snail expression in both ER alpha-negative ES-2 cells and ER alpha-positive SKOV3 cells independent of the existence of ER alpha. The increase of MMP-2 expression in ES-2 and SKOV3 cells and decrease of E-cadherin expression in SKOV3 cells induced by E-2 were associated with up-regulation of Snail. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:623 / 630
页数:8
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