Twist, a master regulator of morphogenesis, plays an essential role in tumor metastasis

被引:3131
作者
Yang, J
Mani, SA
Donaher, JL
Ramaswamy, S
Itzykson, RA
Come, C
Savagner, P
Gitelman, I
Richardson, A
Weinberg, RA
机构
[1] Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
[2] Broad Inst, Canc Genom Program, Cambridge, MA 02141 USA
[3] MGH Ctr Canc Res, Charlestown, MA 02129 USA
[4] Ecole Normale Super, F-75230 Paris 05, France
[5] INSERM, EMI 0229, CRLC Val Aurelle Paul Lamarque, F-34298 Montpellier 5, France
[6] Ben Gurion Univ Negev, Dept Mol Genet & Dev, IL-84105 Beer Sheva, Israel
[7] Harvard Univ, Brigham & Womens Hosp, Sch Med, Dept Pathol, Boston, MA 02115 USA
关键词
D O I
10.1016/j.cell.2004.06.006
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
Metastasis is a multistep process during which cancer cells disseminate from the site of primary tumors and establish secondary tumors in distant organs. In a search for key regulators of metastasis in a murine breast tumor model, we have found that the transcription factor Twist, a master regulator of embryonic morphogenesis, plays an essential role in metastasis. Suppression of Twist expression in highly metastatic mammary carcinoma cells specifically inhibits their ability to metastasize from the mammary gland to the lung. Ectopic expression of Twist results in loss of E-cadherin-mediated cell-cell adhesion, activation of mesenchymal markers, and induction of cell motility, suggesting that Twist contributes to metastasis by promoting an epithelial-mesenchymal transition (EMT). In human breast cancers, high level of Twist expression is correlated with invasive lobular carcinoma, a highly infiltrating tumor type associated with loss of E-cadherin expression. These results establish a mechanistic link between Twist, EMT, and tumor metastasis.
引用
收藏
页码:927 / 939
页数:13
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