Lung CSC‐derived exosomal miR‐210‐3p contributes to a pro‐metastatic phenotype in lung cancer by targeting FGFRL1 - Wang, Li; He, Jun; Hu, Haoyue; Tu, Li; Sun, Zhen; Liu, Yanyang; Luo, Feng (Journal of cellular and molecular medicine, 2020)
Keywords: Antibodies; Base Sequence; Bioinformatics; Biosynthesis; Biotechnology; Cell culture; Cell interactions; Cell Line, Tumor; Endocytosis; exosome; Exosomes; Exosomes - metabolism; Exosomes - ultrastructure; Fibroblast growth factors; Gene Expression Regulation, Neoplastic; Gene Silencing; Genotype & phenotype; Growth factors; Humans; Lung cancer; lung cancer stem cell; Lung Neoplasms - genetics; Lung Neoplasms - pathology; Membrane vesicles; Metastases; Metastasis; MicroRNAs; MicroRNAs - genetics; MicroRNAs - metabolism; miR‐210‐3p; Neoplastic Stem Cells - metabolism; Original; Phenotype; Phenotypes; Proteins; Receptor, Fibroblast Growth Factor, Type 5 - metabolism; Spheres; Spheroids, Cellular - metabolism; Spheroids, Cellular - pathology; Stem cells; Therapeutic applications; Tumor microenvironment; Tumors; Vimentin; Beijing China; China; lung cancer stem cell; miR-210-3p; metastasis; exosome