The Institute of Genetics and Cytology, Northeast Normal University, Changchun, People's Republic of China.
PLoS One. 2011;6(7):e22666. doi: 10.1371/journal.pone.0022666. Epub 2011 Jul 28.
Epithelial to mesenchymal transition (EMT) plays an important role in many biological processes. The latest studies revealed that aggressive breast cancer, especially the triple-negative breast cancer (TNBC) subtype was frequently associated with apparent EMT, but the mechanisms are still unclear. NEDD9/HEF1/Cas-L is a member of the Cas protein family and was identified as a metastasis marker in multiple cancer types. In this study, we wished to discern the role of NEDD9 in breast cancer progression and to investigate the molecular mechanism by which NEDD9 regulates EMT and promotes invasion in triple-negative breast cancer. We showed that expression of NEDD9 was frequently upregulated in TNBC cell lines, and in aggressive breast tumors, especially in TNBC subtype. Knockdown of endogenous NEDD9 reduced the migration, invasion and proliferation of TNBC cells. Moreover, ectopic overexpression of NEDD9 in mammary epithelial cells led to a string of events including the trigger of EMT, activation of ERK signaling, increase of several EMT-inducing transcription factors and promotion of their interactions with the E-cadherin promoter. Data presented in this report contribute to the understanding of the mechanisms by which NEDD9 promotes EMT, and provide useful clues to the evaluation of the potential of NEDD9 as a responsive molecular target for TNBC chemotherapy.
上皮间质转化(EMT)在许多生物学过程中起着重要作用。最新研究表明,侵袭性乳腺癌,尤其是三阴性乳腺癌(TNBC)亚型,常伴有明显的 EMT,但机制尚不清楚。NEDD9/HEF1/Cas-L 是 Cas 蛋白家族的一员,被鉴定为多种癌症类型的转移标志物。在本研究中,我们希望探讨 NEDD9 在乳腺癌进展中的作用,并研究 NEDD9 调节 EMT 并促进三阴性乳腺癌侵袭的分子机制。我们发现,NEDD9 在 TNBC 细胞系中的表达经常上调,在侵袭性乳腺癌肿瘤中,特别是在 TNBC 亚型中上调更为明显。内源性 NEDD9 的敲低降低了 TNBC 细胞的迁移、侵袭和增殖。此外,NEDD9 在乳腺上皮细胞中的异位过表达导致一系列事件的发生,包括 EMT 的触发、ERK 信号的激活、几个 EMT 诱导转录因子的增加以及促进它们与 E-钙黏蛋白启动子的相互作用。本报告中提供的数据有助于理解 NEDD9 促进 EMT 的机制,并为评估 NEDD9 作为 TNBC 化疗的反应性分子靶标提供了有用的线索。