Godin, F., Villette, S., Vallée, B., Doudeau, M., Morisset-Lopez, S., Ardourel, M., Hevor, T., Pichon, C. and Bénédetti, B.
Biochemical and Biophysical Research Communications (sous presse) doi:10.1016/j.bbrc.2012.01.079
Neurofibromatosis type 1 is a common genetic disease that causes nervous system tumors, and cognitive deficits. It is due to mutations within the NF1 gene, which encodes the Nf1 protein. Nf1 has been shown to be involved in the regulation of Ras, cAMP and actin cytoskeleton dynamics. In this study, using immunofluorescence
experiments, we have shown a partial nuclear localization of Nf1 in the astrocytoma cell
line: CCF and we have demonstrated that Nf1 partially colocalizes with PML (promyelocytic leukemia) nuclear bodies. A direct interaction between Nf1 and the multiprotein complex has further been demonstrated using ‘‘in situ’’ proximity ligation assay (PLA).
“Imaging of diagnostic and therapeutic biomarkers in Oncology” Workshop.
TAX2 peptide: from discovery to clinical development.