Ontology highlight
ABSTRACT: Background/aim
We examined the gene expression changes of breast cancer cells spontaneously undergoing epithelial-mesenchymal transition (EMT) and its reverse process mesenchymal-epithelial transition (MET) and the role of exosomes in these transitions.Materials and methods
Highly invasive mesenchymal-like breast cancer cells, MDA-MB-231 (basal cells), EMT and MET variants, were characterized by microarray gene expression profiling, immunocytochemistry and chemo-sensitivity.Results
Spontaneously disseminated cells were anoikis resistant, exhibited a dissociative, EMT-like phenotype and underwent MET when reseeded in cell-free plates. MET was inhibited by exosomes secreted by basal cells. Chemo-sensitivity to doxorubicin, vincristine and paclitaxel decreased in the order EMT
SUBMITTER: Bigagli E
PROVIDER: S-EPMC6542641 | biostudies-literature | 2019 May-Jun
REPOSITORIES: biostudies-literature
Bigagli Elisabetta E Cinci Lorenzo L D'Ambrosio Mario M Luceri Cristina C
Cancer genomics & proteomics 20190501 3
<h4>Background/aim</h4>We examined the gene expression changes of breast cancer cells spontaneously undergoing epithelial-mesenchymal transition (EMT) and its reverse process mesenchymal-epithelial transition (MET) and the role of exosomes in these transitions.<h4>Materials and methods</h4>Highly invasive mesenchymal-like breast cancer cells, MDA-MB-231 (basal cells), EMT and MET variants, were characterized by microarray gene expression profiling, immunocytochemistry and chemo-sensitivity.<h4>R ...[more]