The role of HEF1/NEDD9 protein in proliferation and invasion of metastatic breast cancer

点击翻译按钮获取中文摘要

 DESCRIPTION (provided by applicant): HEF1/NEDD9 is a cytoplasmic adaptor protein and a well-established marker of poor prognosis in different cancers with invasive tumor signature. We have previously reported that NEDD9 regulates stability and activation of mitotic kinase AurA/AURKA leading to phosphorylation of multiple cytoplasmic substrates, such as HDAC6, Src, CTTN, Arp/C and cofilin involved in migration and invasion. Our novel findings indicate that decrease in NEDD9 expression in TNBCs leads to translocation of AURKA to the nucleus. Presence of nuclear AURKA correlates with increase in metastatic colonization and sensitivity to AURKA inhibitors, but molecular mechanisms of this phenomenon and its role in tumor progression and metastasis is currently unknown. Interestingly, depletion of NEDD9 in HER2+ cancers decreases metastasis, thus suggesting differential role of NEDD9 in HER2+ BCs. Our novel findings indicate that NEDD9 emerges as a critical regulator of proliferation and sensitivity of HER2+ breast cancers to Herceptin via regulation of HER2 trafficking/recycling. The objective of this application is to determine the role of nuclear AURKA in metastasis in TN and HER2+ breast cancers using characterized cell lines, patient-derived xenografts and a conditional NEDD9 knock-in mouse model. Our central hypothesis is that NEDD9 is required for retention of AURKA in the cytoplasm to promote migration/invasion of tumor cells and a decrease in NEDD9 leads to nuclear translocation of AURKA, thus promoting cell survival in the metastatic niche of TNBCs. Furthermore, upregulation of NEDD9 in HER2+ BCs will lead to an increase in tumor incidence and disease progression. We will test this hypothesis by execution of the following aims: AIM 1. Determine the role of NEDD9 in AURKA cytoplasmic/nuclear translocation and the impact of nuclear AURKA on metastasis. Our hypothesis is that nuclear AURKA promotes survival and resistance to apoptosis, through the inactivation TFEB and activation of NUPR1 and Sox2 pathways. AIM 2. Elucidate the role and mechanisms by which overexpression of NEDD9 promotes HER2+ breast cancer using genetically modified mouse models and patient derived xenografts. Our hypothesis is that overexpression of NEDD9 heightens HER2-driven tumorigenesis and confers Herceptin resistance via upregulation of HER2 protein and recycling via late endosomes.