101. The p53 family member p73 modulates the proproliferative role of IGFBP3 in short children born small for gestational age.
- Author
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Marzano F, Ventura A, Caratozzolo MF, Aiello I, Mastropasqua F, Brunetti G, Cavallo L, Sbisà E, Faienza MF, and Tullo A
- Subjects
- Base Sequence, Cell Proliferation physiology, Cells, Cultured, Child, DNA-Binding Proteins genetics, Female, Genes, p53, HCT116 Cells, HEK293 Cells, Human Growth Hormone metabolism, Humans, Infant, Infant, Newborn, Infant, Small for Gestational Age, Insulin-Like Growth Factor Binding Protein 1 genetics, Insulin-Like Growth Factor Binding Protein 3 genetics, MCF-7 Cells, Male, Molecular Sequence Data, Nuclear Proteins genetics, Transfection, Tumor Protein p73, Tumor Suppressor Proteins genetics, DNA-Binding Proteins metabolism, Insulin-Like Growth Factor Binding Protein 1 metabolism, Insulin-Like Growth Factor Binding Protein 3 metabolism, Nuclear Proteins metabolism, Tumor Suppressor Proteins metabolism
- Abstract
The regulation of insulin-like growth factor-binding protein 3 (IGFBP3) gene expression is complex, because it can be induced by agents that both stimulate and inhibit the proliferation. The principal aim of this study was to investigate whether p73, a member of the p53 gene family, has a role in the regulation of the IGFBP3 expression and whether this regulation occurs in a context of cell survival or death. We demonstrate that IGFBP3 is a direct TAp73α (the p73 isoform that contains the trans-activation domain) target gene and activates the expression of IGFBP3 in actively proliferating cells. As IGFBP3 plays a key role in regulating the growth hormone/insulin-like growth factor type 1 (GH/IGF1) axis, whose alterations in gene expression appear to have a role in the growth failure of children born small for gestational age (SGA), we measured the mRNA expression levels of p73 and IGFBP3 in a group of SGA children. We found that mRNA expression levels of p73 and IGFBP3 are significantly lower in SGA children compared with controls and, in particular, p73 mRNA expression is significantly lower in SGA children with respect to height. Our results shed light on the intricate GH/IGF pathway, suggesting p73 as a good biomarker of the clinical risk for SGA children to remain short in adulthood., (© 2015 Marzano et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0).)
- Published
- 2015
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