EWI-2 controls nucleocytoplasmic shuttling of EGFR signaling molecules and miRNA sorting in exosomes to inhibit prostate cancer cell metastasis.
Chenying FuQing ZhangAni WangSongpeng YangYangfu JiangLin BaiQuan WeiPublished in: Molecular oncology (2021)
Early and accurate diagnosis of prostate cancer (PCa) is extremely important, as metastatic PCa remains hard to treat. EWI-2, a member of the Ig protein subfamily, is known to inhibit PCa cell migration. In this study, we found that EWI-2 localized on both the cell membrane and exosomes regulates the distribution of miR-3934-5p between cells and exosomes. Interestingly, we observed that EWI-2 is localized not only on the plasma membrane but also on the nuclear envelope (nuclear membrane), where it regulates the nuclear translocation of signaling molecules and miRNA. Collectively, these functions of EWI-2 found in lipid bilayers appear to regulate PCa cell metastasis through the epidermal growth factor receptor-mitogen-activated protein kinase-extracellular-signal-regulated kinase (EGFR-MAPK-ERK) pathway. Our research provides new insights into the molecular function of EWI-2 on PCa metastasis, and highlights EWI-2 as a potential PCa biomarker.
Keyphrases
- epidermal growth factor receptor
- tyrosine kinase
- prostate cancer
- small cell lung cancer
- cell migration
- mesenchymal stem cells
- advanced non small cell lung cancer
- stem cells
- signaling pathway
- induced apoptosis
- pi k akt
- squamous cell carcinoma
- radical prostatectomy
- single cell
- oxidative stress
- protein kinase
- molecular dynamics simulations
- cell therapy
- cell cycle arrest
- cell proliferation
- transcription factor
- small molecule
- risk assessment
- amino acid
- binding protein
- genome wide identification