关键词: EMT FMRP TNBC cell invasion mRNA metabolism

Mesh : Animals Breast Neoplasms / metabolism pathology Cadherins / metabolism Cell Adhesion Cell Line, Tumor Cell Movement Cell Shape Disease Progression Epithelial-Mesenchymal Transition Female Fragile X Mental Retardation Protein / antagonists & inhibitors genetics metabolism Humans Immunohistochemistry Lung Neoplasms / metabolism pathology secondary Mice RNA Interference RNA, Messenger / metabolism RNA, Small Interfering / metabolism Vimentin / metabolism

来  源:   DOI:10.1002/emmm.201302847   PDF(Sci-hub)

Abstract:
The role of the fragile X mental retardation protein (FMRP) is well established in brain, where its absence leads to the fragile X syndrome (FXS). FMRP is almost ubiquitously expressed, suggesting that, in addition to its effects in brain, it may have fundamental roles in other organs. There is evidence that FMRP expression can be linked to cancer. FMR1 mRNA, encoding FMRP, is overexpressed in hepatocellular carcinoma cells. A decreased risk of cancer has been reported in patients with FXS while a patient-case with FXS showed an unusual decrease of tumour brain invasiveness. However, a role for FMRP in regulating cancer biology, if any, remains unknown. We show here that FMRP and FMR1 mRNA levels correlate with prognostic indicators of aggressive breast cancer, lung metastases probability and triple negative breast cancer (TNBC). We establish that FMRP overexpression in murine breast primary tumours enhances lung metastasis while its reduction has the opposite effect regulating cell spreading and invasion. FMRP binds mRNAs involved in epithelial mesenchymal transition (EMT) and invasion including E-cadherin and Vimentin mRNAs, hallmarks of EMT and cancer progression.
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