Transforming growth factor-α induces human ovarian cancer cell invasion by down-regulating E-cadherin in a Snail-independent manner

被引:20
|
作者
Qiu, Xin [1 ]
Cheng, Jung-Chien [1 ]
Klausen, Christian [1 ]
Fan, Qianlan [1 ]
Chang, Hsun-Ming [1 ]
So, Wai-Kin [1 ]
Leung, Peter C. K. [1 ]
机构
[1] Univ British Columbia, Child & Family Res Inst, Dept Obstet & Gynaecol, Vancouver, BC V5Z 4H4, Canada
基金
加拿大健康研究院;
关键词
TGF-alpha; E-cadherin; Ovarian cancer; Slug; Snail; HER2; REPRESSES E-CADHERIN; FACTOR RECEPTOR; EGF RECEPTOR; CLINICAL-SIGNIFICANCE; MICE LACKING; AMPHIREGULIN; EXPRESSION; SLUG; BREAST;
D O I
10.1016/j.bbrc.2015.03.180
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Transforming growth factor-alpha (TGF-alpha), like epidermal growth factor (EGF) and amphiregulin (AREG) binds exclusively to EGF receptor (EGFR). We have previously demonstrated that EGF, AREG and TGF-alpha down-regulate E-cadherin and induce ovarian cancer cell invasion, though whether these ligands use the same molecular mediators remains unknown. We now show that, like EGF, TGF-alpha- and AREG-induced E-cadherin down-regulation involves both EGFR and HER2. However, in contrast to EGF and AREG, the transcription factor Snail is not required for TGF-alpha-induced E-cadherin down-regulation. This study shows that TGF-alpha uses common and divergent molecular mediators to regulate E-cadherin expression and cell invasion. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:128 / 135
页数:8
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