The high mobility group A (
HMGA) proteins are thought to work as ancillary
transcription factors and to regulate the expression of a growing number of genes through direct binding to
DNA or via
protein-
protein interactions. Both HMGA1 and HMGA2 are important regulators of basic biological processes, including cell growth, differentiation and transformation. Their qualitatively or quantitatively altered expression has been described in a number of human
tumors. We studied and review here their expression in neuroblastic
tumors. HMGA2 is expressed only in a subset of ex vivo
neuroblastoma (NB)
tumors and in the embryonic adrenal gland, but it is undetectable in the adult adrenal gland, suggesting that its anomalous expression might be associated with NB
tumorigenesis and/or
tumor progression. In vitro, its expression is easily detectable in
retinoic acid (RA)-resistant cell lines. The exogenous expression of HMGA2 is sufficient to convert RA-sensitive SY5Y NB cells into RA-resistant cells, thus suggesting that HMGA2 might be a relevant player in determining NB cell responses to endogenous or therapeutically important growth inhibitory substances. In contrast, HMGA1 expression is readily detectable in all NB cell lines and
tumors, but its expression is consistently higher in less differentiated NBs compared with
ganglioneuromas and
ganglioneuroblastomas. Interestingly, RA increases HMGA1 expression in RA-resistant NB cells but inhibits it in cells undergoing RA-induced growth inhibition and neuronal differentiation. Our studies indicate that
HMGA molecules might be biologically and pathologically relevant factors in neuroblastic
tumor development and progression.