Expression of the beta 4 integrin subunit induces monocytic differentiation of 32D/v-Abl cells
Polcini, Alessandro Tartaglia
Mercurio, Arthur M.
UMass Chan AffiliationsDepartment of Cancer Biology
Cell Line, Transformed
Genes, Tumor Suppressor
Mitogen-Activated Protein Kinases
Oncogene Proteins v-abl
Tumor Suppressor Proteins
tumor suppressor protein p73
Amino Acids, Peptides, and Proteins
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AbstractThe alpha 6 beta 4 integrin is the receptor for various laminin isoforms and is a component of the hemidesmosome. Increased expression levels of this integrin correlate with the aggressive phenotype of many epithelial tumors compared with surrounding normal tissue. Furthermore, the long cytoplasmic tail of the beta 4 integrin subunit has been implicated in several signal transduction pathways that are involved not only in invasion, but also in proliferation and apoptosis. Here we report that the exogenous expression of beta 4 integrin in 32D/v-abl-transformed cells reduces tumor aggressiveness in vivo and strongly inhibits cell proliferation in vitro by inducing monocytic differentiation. These effects are accompanied by growth arrest and p73 protein accumulation. The hypothesis that the inhibition of v-Abl oncogenic capacity could allow the activation of the endogenous c-Abl was tested in RKO cells. The results clearly demonstrated a strong increase of c-Abl phosphorylation that is accompanied by its association with p73 protein. Overall, the reported findings indicate that alpha 6 beta 4 integrin promotes growth arrest and differentiation by modulating Abl kinases and p73 protein pathway(s).
Blood. 2002 Jul 1;100(1):96-106.
Permanent Link to this Itemhttp://hdl.handle.net/20.500.14038/26245
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