作者: Fahd Al-Mulla , Jean Paul Thiery , Tan Tuan Zea , Devasis Chatterjee , Kam C Yeung
DOI:
关键词: Cancer research 、 Proliferative index 、 Epithelial–mesenchymal transition 、 Metastasis suppressor 、 MAPK/ERK pathway 、 Progesterone receptor 、 Estrogen receptor 、 Claudin-Low 、 Medicine 、 Breast cancer
摘要: Raf Kinase inhibitory protein (RKIP) is a well-established metastasis suppressor that frequently downregulated in aggressive cancers. The impact of RKIP and its phosphorylated form on disease-free survival (DFS) other clinicopathological parameters breast cancer yet to be discovered. To this end, we examined expression 3 independent cohorts. At the Protein level, loss or reduced total was associated with large-sized tumors characterized by high proliferative index, high-grade diminished estrogen (ER) progesterone receptor expression. Loss diminution significantly shorter DFS all Moreover, complete p-RKIP an prognostic factor using multivariate analysis operable invasive ductal cancer. We show for first time ER, partly, drives through MTA3-Snail axis. Consistent finding, found that, at mRNA varied across different molecular subtypes Luminal (ER+) subtype expressing levels more Claudin-low (ER-) subtype, which depicted highest epithelial mesenchymal transition (EMT) registered lowest levels. In conclusion, expression/diminution poor diseases-free Determining adds significant value management subtyping disease.