转移
RAC1
基因沉默
癌症研究
乳腺癌
癌症
体内
转移性乳腺癌
乳腺癌转移
化学
生物
癌症转移
医学
细胞生物学
内科学
基因
信号转导
生物化学
遗传学
作者
Yong Teng,Haiyan Qin,Abdulaziz Bahassan,N. George Bendzunas,Eileen J. Kennedy,John K. Cowell
出处
期刊:Cancer Research
[American Association for Cancer Research]
日期:2016-07-18
卷期号:76 (17): 5133-5142
被引量:74
标识
DOI:10.1158/0008-5472.can-16-0562
摘要
Inactivation of the WASF3 gene suppresses invasion and metastasis of breast cancer cells. WASF3 function is regulated through a protein complex that includes the NCKAP1 and CYFIP1 proteins. Here, we report that silencing NCKAP1 destabilizes the WASF3 complex, resulting in a suppression of the invasive capacity of breast, prostate, and colon cancer cells. In an in vivo model of spontaneous metastasis in immunocompromized mice, loss of NCKAP1 also suppresses metastasis. Activation of the WASF protein complex occurs through interaction with RAC1, and inactivation of NCKAP1 prevents the association of RAC1 with the WASF3 complex. Thus, WASF3 depends on NCKAP1 to promote invasion and metastasis. Here, we show that stapled peptides targeting the interface between NCKAP1 and CYFIP1 destabilize the WASF3 complex and suppress RAC1 binding, thereby suppressing invasion. Using a complex-disrupting compound identified in this study termed WANT3, our results offer a mechanistic proof of concept to target this interaction as a novel approach to inhibit breast cancer metastasis. Cancer Res; 76(17); 5133-42. ©2016 AACR.
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